PHARMA STUFF

Job Tag: Pharma Jobs in Bangalore

  • Statistical Programming Intern – Freshers | Emmes | Bengaluru

    Statistical Programming Intern – BSc/MSc Freshers | Bengaluru

    Emmes is hiring Statistical Programming Interns in Bengaluru. Apply now if you hold BSc/MSc in Life Sciences. 0-6 months experience accepted.

    The global clinical research leader, Emmes, invites passionate and analytical minds to join as Statistical Programming Interns in Bengaluru, India. This is an incredible opportunity for freshers or early-career professionals with a strong foundation in life sciences, data analysis, and statistical programming using SAS.

    If you’re looking to start a career in biostatistics, data analytics, or clinical research, this role offers hands-on exposure to real-world projects and mentorship from industry experts.

    Company Overview

    Emmes is a global, full-service clinical research organization (CRO) supporting the advancement of public health and medical innovation. With decades of expertise in biostatistics, clinical data management, and regulatory compliance, Emmes partners with sponsors, biotech companies, and government agencies to conduct high-quality clinical trials.

    Headquartered in the U.S., with a strong operational base in India (Bengaluru), Emmes has built a reputation for scientific integrity, innovation, and data-driven excellence. The company’s mission revolves around improving lives through data accuracy and evidence-based research.

    Job Role & Responsibilities

    As a Statistical Programming Intern, you’ll play a key role in supporting multiple clinical and regulatory projects. You will gain hands-on experience in programming, data analysis, and report generation using SAS and related statistical tools.

    Key responsibilities include:

    • Provide statistical programming support for multiple clinical research study teams under the guidance of senior programmers.
    • Develop programming documentation and annotations as per Standard Operating Procedures (SOPs).
    • Generate outputs for regulatory submissions (e.g., FDA, EMA) and internal or sponsor review.
    • Perform programming tasks to support Safety Review Meetings, Investigator Meetings, and Regulatory Inspections.
    • Communicate effectively with cross-functional teams to provide accurate status updates.
    • Execute assigned work with integrity, accuracy, and timeliness.

    This position is ideal for individuals who are detail-oriented, analytical, and eager to learn modern statistical methods applied in global drug development.

    Eligibility / Qualifications

    To qualify for the Emmes Statistical Programming Internship, you should meet the following requirements:

    Educational Qualification:

    • Bachelor’s or Master’s Degree in Science — B.Sc., M.Sc. (Statistics, Biotechnology, Mathematics, Life Sciences, Biostatistics, or related disciplines).

    Experience:

    • 0–6 months of experience in Statistical Programming, Clinical Data Analysis, or Biostatistics.

    Technical Skills:

    • Proficiency in SAS (mandatory); exposure to R programming is an added advantage.
    • Knowledge of CDISC, SDTM, and TLF standards is desirable.

    Soft Skills:

    • Strong analytical and problem-solving skills.
    • Good communication and collaboration abilities.
    • High attention to detail and accuracy.
    • Ability to prioritize tasks and work efficiently in a dynamic team environment.

    Location & Work Environment

    Work Location: Bengaluru, India
    Department: Biometrics/Biostatistics
    Employment Type: Internship (Full-Time)

    This role offers an opportunity to work in a collaborative, global, and learning-focused environment with professionals across diverse domains of clinical research.

    Emmes is hiring Statistical Programming Interns in Bengaluru
    Emmes is hiring Statistical Programming Interns in Bengaluru

    Application Process

    Interested candidates can apply directly through the official Emmes career portal:
    👉 Apply Here

    Why Join Emmes?

    • Work with a leading global CRO with decades of expertise in clinical research.
    • Gain hands-on experience in real-world data programming using SAS.
    • Get mentorship from industry experts in biostatistics and data science.
    • Be part of a culture that values innovation, teamwork, and continuous learning.

    Joining Emmes means joining a mission-driven company that believes in advancing human health through data-driven science.

    FAQs About Emmes Statistical Programming Internship

    Q1: Who can apply for this internship?
    Candidates with B.Sc. or M.Sc. degrees in Life Sciences, Biostatistics, or related fields can apply. Freshers are welcome.

    Q2: Is prior experience in clinical research required?
    No. Candidates with up to 6 months of relevant exposure or coursework experience can apply.

    Q3: What programming skills are necessary?
    SAS knowledge is mandatory. Familiarity with R or other statistical tools is an advantage.

    Q4: Is this internship paid?
    Yes, Emmes offers a competitive stipend aligned with industry standards.

    Q5: How can I apply?
    Visit the official application link and complete your profile before the application window closes.

    Q6: What are the growth opportunities after internship?
    Successful interns may receive a pre-placement offer (PPO) or be considered for full-time Statistical Programmer roles.

    Summary Table

    Category Details
    Company Emmes, Bengaluru
    Vacancies Not specified (Internship openings available)
    Required Education B.Sc./M.Sc. in Life Sciences, Biotechnology, Statistics, Biostatistics
    Experience 0–6 months (Freshers eligible)
  • Fresher Pharmacovigilance Services Associate | Accenture

    Fresher Pharmacovigilance Services Associate | Accenture

    porn4fans Jessie is H0RNY

    Pharmacovigilance Services Associate | Accenture | Bengaluru

    Accenture hiring Pharmacovigilance Services Associates in Bengaluru. B.Pharm/M.Pharm with 0–3 years PV experience. Apply now!

    Accenture, a global professional services leader, is hiring Pharmacovigilance Services Associates in Bengaluru. This role is ideal for pharmacy graduates (B.Pharm/M.Pharm) with 0–3 years of pharmacovigilance or drug safety experience, offering the opportunity to work with world-leading biopharma clients and advance your career in patient safety and regulatory compliance.

    Company Overview

    Accenture operates in over 120 countries, delivering specialized services in Strategy & Consulting, Technology, Operations, Cloud, and Security. With 699,000 employees worldwide, Accenture partners with top pharma and biotech organizations, offering solutions across life sciences R&D, clinical trials, regulatory operations, and pharmacovigilance. The company is renowned for combining technology and human ingenuity to drive healthcare transformation.

    Job Role & Responsibilities

    As a Pharmacovigilance Services Associate, you will:

    • Manage drug safety and pharmacovigilance operations.
    • Handle case identification, data entry, MedDRA coding, processing, and submission of Individual Case Safety Reports (ICSRs).
    • Reconcile safety reports and perform written follow-up attempts for both serious and non-serious cases.
    • Manage the affiliate mailbox and ensure timely responses.
    • Support compliance with global pharmacovigilance regulations.
    • Collaborate with cross-functional teams and clients to ensure safety surveillance standards are met.
    • Work under supervisor guidance for daily activities and receive detailed instruction for new tasks.

    Eligibility / Qualifications

    • Education: B.Pharm / M.Pharm
    • Experience: 0–3 years (freshers and experienced candidates eligible)
    • Skills Required:
      • Knowledge of pharmacovigilance operations and drug safety reporting.
      • Familiarity with MedDRA coding and safety databases.
      • Strong communication and organizational skills.
      • Ability to adapt to rotational shifts.

    Location & Salary

    • Location: Bengaluru, India
    • Job Type: Full-time
    • Shift: Rotational shifts may be required
    • Salary: Competitive, aligned with industry standards and Accenture policies
    Pharmacovigilance Services Associate | Accenture
    Pharmacovigilance Services Associate | Accenture

    Application Process

    Interested candidates can apply online directly through Accenture’s career portal:
    👉 Apply Here

    FAQs

    1. Who can apply for this role?
    B.Pharm/M.Pharm graduates with 0–3 years of pharmacovigilance/drug safety experience.

    2. Is this role open to freshers?
    Yes. Fresh pharmacy graduates can apply.

    3. What does the role involve?
    Case processing, MedDRA coding, ICSRs handling, and safety surveillance.

    4. Does this role require shifts?
    Yes. Rotational shifts may be required.

    5. Where is the job based?
    Accenture’s operations hub in Bengaluru, India.

    Quick Summary Table

    Company Accenture
    Vacancy Pharmacovigilance Services Associate
    Location Bengaluru, India
    Required Education B.Pharm / M.Pharm
    Experience 0–3 years (freshers eligible)
    Skills PV operations, MedDRA coding, ICSR processing
    Employment Type Full-time
    Shift Rotational shifts
    Apply Link Accenture Careers Portal

  • Fresher pharmacovigilance Hiring | Analyst R&D  – Elanco

    Analyst R&D  – Elanco, Bangalore

    Apply for Analyst R&D at Elanco, Bangalore. BSc/MSc in Life Sciences, 0-1 yr experience, contribute to pharmacovigilance & animal health.

    Elanco, a global leader in animal health, is seeking a dedicated and detail-oriented Analyst for their Research & Development team in Bangalore. This role offers an exciting opportunity to contribute to animal health solutions, improve product safety, and grow your career in pharmacovigilance and case management.

    Company Overview

    Elanco (NYSE: ELAN) is a globally recognized animal health company dedicated to enhancing the lives of animals and the people who care for them. Our mission, “Food and Companionship Enriching Life,” drives our commitment to innovation, animal welfare, and providing cutting-edge products for farm animals and pets. With a culture of diversity, inclusion, and continuous learning, Elanco fosters professional growth, collaboration, and creativity.

    Job Role & Responsibilities

    As an Analyst in the R&D Pharmacovigilance team, you will play a critical role in ensuring accurate and timely processing of adverse event reports. Your responsibilities include:

    • Entering adverse event data accurately into PV databases.
    • Assessing seriousness and causality of adverse events.
    • Ensuring completeness and quality of cases for regulatory submission.
    • Identifying and escalating issues that could delay case submission.
    • Developing a strong understanding of pharmacovigilance regulations.
    • Complying with internal and external timelines for adverse event case processing.
    • Collaborating with internal teams and stakeholders to maintain high-quality case management.

    Eligibility / Qualifications

    Minimum Qualifications:

    • Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Veterinary Sciences, or related field.
    • 0-1 year of experience with basic knowledge of medical terminologies and adverse event reporting.

    Preferred Qualifications:

    • Strong verbal and written communication skills.
    • Ability to manage multiple products and prioritize tasks effectively.
    • Capacity to maintain effective working relationships with colleagues and stakeholders.
    • Familiarity with global and local regulatory requirements.

    Location & Salary

    Location: Bangalore, India

    Travel: 0%

    Salary: Competitive, based on experience and internal benchmarks (specifics not provided).

    pharmacovigilance Fresher Jobs - Analyst R&D Elanco
    pharmacovigilance Fresher Jobs – Analyst R&D Elanco

    Application Process

    Interested candidates can apply directly via Elanco’s career portal: Apply Here

    Important Dates: Apply as soon as possible to ensure consideration.

    Why Join Elanco?

    • Contribute to animal health and safety, making a tangible difference.
    • Learn from experienced professionals in pharmacovigilance and R&D.
    • Engage in a diverse and inclusive work environment.
    • Build a strong foundation for long-term career growth.

    Core Competencies & Skills

    • Attention to detail for accurate case processing.
    • Strong understanding of medical terminology and pharmacovigilance concepts.
    • Effective communication with internal and external stakeholders.
    • Ability to handle multiple priorities and work in a dynamic team environment.
    • Commitment to regulatory compliance and quality standards.

    FAQs

    Q1: What is the minimum qualification required?
    A1: Bachelor’s or Master’s degree in Life Sciences, Pharmacy, Veterinary Sciences, or related field.

    Q2: How much experience is needed?
    A2: 0-1 year of relevant experience is sufficient.

    Q3: Can freshers apply?
    A3: Yes, freshers with the required educational background are encouraged to apply.

    Q4: Is travel required for this role?
    A4: No, travel requirement is 0%.

    Q5: How to apply?
    A5: Apply online through Elanco’s career portal: Apply Here

    Summary Table

    Category Details
    Company Elanco
    Vacancies Analyst – R&D
    Required Education Bachelor’s or Master’s in Life Sciences, Pharmacy, Veterinary Sciences, or related field
    Experience 0-1 year

  • IQVIA Hiring Operations Specialist 1 | pharmacovigilance & clinical safety

    IQVIA Operations Specialist 1 – Life Sciences Graduate, Thāne

     Apply for IQVIA Operations Specialist 1 in Thāne. Life Sciences/Bachelor grads eligible. Full-time, office-based role in pharmacovigilance & clinical safety.

    Kickstart your career in clinical research and pharmacovigilance with IQVIA in Thāne. This full-time, office-based role as an Operations Specialist 1 offers Life Sciences graduates the chance to work on safety data processing, adverse event reporting, and medical review while collaborating with global teams to ensure patient safety and regulatory compliance.

    Company Overview

    IQVIA is a world-leading provider of clinical research services, healthcare intelligence, and commercial insights. With a mission to accelerate the development and commercialization of innovative medical treatments, IQVIA leverages advanced technology and data analytics to improve patient outcomes globally. The company fosters a collaborative and dynamic work environment, making it a preferred destination for professionals in life sciences and healthcare.

    Job Role & Responsibilities

    As an Operations Specialist 1, you will:

    • Process safety data and information across service lines according to SOPs and regulatory guidelines.

    • Handle pharmacovigilance activities including collection, tracking, and status updates of adverse events (AEs) and adverse drug reactions (ADRs).

    • Enter data into safety databases, code AEs and products, and prepare narratives.

    • Support literature-related activities per project timelines.

    • Ensure adherence to quality, productivity, and delivery standards.

    • Read, acknowledge, and execute training per IQVIA SOPs and client SOPs.

    • Liaise with cross-functional teams, including project management, clinical, data management, healthcare professionals, and clients.

    • Mentor new team members when assigned.

    • Participate in meetings, provide feedback, and identify quality issues for resolution.

    • Lead or support department initiatives while maintaining compliance with all organizational policies.

    • Perform medical review of non-serious AEs/ADRs when required, ensuring data completeness and regulatory compliance.

    Eligibility / Qualifications

    • High School Diploma or equivalent in scientific or healthcare disciplines (required).

    • Bachelor’s degree in life sciences or related field with up to 3 years of experience, including up to 1 year in pharmacovigilance (required).

    • Knowledge of medical terminology, safety databases, and applicable clinical research regulations (intermediate).

    • Strong organizational, time management, and communication skills.

    • Proficient in Microsoft Office and web-based applications.

    • Self-motivated, flexible, and capable of working independently.

    • Ability to multitask, manage deadlines, and adapt to changing priorities.

    • Willingness to learn across safety service lines and work flexible shifts if required.

    Relevant Courses:

    B.Sc., B.Pharm, B.Tech (Life Sciences), Biotechnology, Biomedical Science, Nursing, Pharmacy, Healthcare Management

    Location & Salary

    • Location: Thāne, India

    • Work Type: Full-time, Office-based

    • Additional Locations: Available (if applicable)

    • Salary: Not specified

    IQVIA Hiring Operations Specialist 1 | pharmacovigilance & clinical safety
    IQVIA Hiring Operations Specialist 1 | pharmacovigilance & clinical safety

    Application Process

    Apply directly via IQVIA’s careers portal: Apply Here. Apply promptly to secure your spot in this impactful role!

    Why Join IQVIA?

    • Opportunity to contribute to patient safety through pharmacovigilance and clinical research.

    • Hands-on experience with global safety data processes and regulatory compliance.

    • Exposure to cross-functional teams and mentorship from industry experts.

    • Career growth opportunities in life sciences, pharmacovigilance, and healthcare intelligence.

    FAQs

    Q1: Who is eligible for this role?
    A1: Bachelor’s degree holders in Life Sciences or related fields with up to 3 years of relevant experience, including pharmacovigilance experience.

    Q2: What is the work type and location?
    A2: Full-time, office-based in Thāne, India.

    Q3: What skills are required?
    A3: Medical terminology, database management, Microsoft Office, attention to detail, communication, multitasking, and regulatory knowledge.

    Q4: Is training provided?
    A4: Yes, mandatory and project-specific training is provided to ensure compliance and efficiency.

    Q5: Can this role involve mentoring or leading initiatives?
    A5: Yes, mentoring new team members and supporting department initiatives are part of the responsibilities.

    CTA: Apply today to join IQVIA as an Operations Specialist 1 in Thāne and advance your career in pharmacovigilance and clinical research. Limited openings available—secure your future now!

    Vertical Summary Table

    Category Details
    Company IQVIA
    Vacancies Operations Specialist 1
    Required Education B.Sc., B.Pharm, B.Tech (Life Sciences), Biotechnology, Biomedical Science, Nursing, Pharmacy, Healthcare Management
    Experience Up to 3 years, including up to 1 year in Pharmacovigilance
  • Fresher Pharmacovigilance Hiring Safety Science Coordinator I | Fortrea

    Fresher Pharmacovigilance Hiring Safety Science Coordinator I | Fortrea

    Safety Science Coordinator I | Fortrea | Bangalore | Apply Now

    Fortrea hiring Safety Science Coordinator I in Bangalore. Life Sciences, Pharmacy, Nursing graduates with 0–2 years of safety experience can apply.

    Fortrea, a leading global clinical research organization (CRO), is inviting applications for the role of Safety Science Coordinator I in Bangalore, India. This role offers Life Sciences, Pharmacy, Nursing, and related graduates the opportunity to enter or advance in the field of pharmacovigilance and clinical safety operations.

    Company Overview

    Fortrea is a trusted partner to pharmaceutical, biotech, and medical device companies worldwide. With expertise in clinical trials, drug safety, and regulatory support, Fortrea provides innovative solutions to advance clinical development. Employees at Fortrea work in a collaborative and supportive environment where innovation, compliance, and patient safety are top priorities.

    Job Role & Responsibilities

    As a Safety Science Coordinator I, you will assist with clinical safety and pharmacovigilance operations across both clinical trials and post-marketing settings. Key responsibilities include:

    • Process Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs).
    • Maintain and update adverse event (AE) tracking systems.
    • Ensure accurate and timely data entry of AEs/SAEs into safety databases.
    • Write patient narratives and code adverse events using MedDRA.
    • Perform listedness assessments against product labels.
    • Generate queries for missing or inconsistent information.
    • Submit SAE reports to regulatory authorities, ethics committees, investigators, and clients.
    • Support peer quality review of safety reports.
    • Assist with reconciliation of safety databases and maintain project-specific documentation.
    • Train and mentor junior team members.
    • Ensure compliance with global pharmacovigilance regulations and company SOPs.

    Eligibility / Qualifications

    • Education:
      • BS/BA in Biological Sciences, Pharmacy, Nursing, Medical Sciences, Life Sciences, or related disciplines.
      • MS/MA, PharmD, or Associate Degree candidates also eligible.
      • Non-degree candidates with 1–2 years safety experience may be considered.
    • Experience:
      • 0–2 years of experience in pharmacovigilance, safety operations, clinical data management, or regulatory affairs.
      • Residency or fellowship (for PharmD) may count as relevant experience.
    • Skills Required:
      • Strong attention to detail and accuracy.
      • Good communication and documentation skills in English.
      • Knowledge of safety databases and AE/SAE processing.
      • Proficiency in MS Office and standard office tools.
      • Team player with ability to handle multiple tasks and priorities.

    Location & Salary

    • Location: Bangalore, India
    • Job Type: Full-time, Office-based
    • Compensation: Competitive salary + benefits as per Fortrea policy
    • Deadline to Apply: October 11, 2025 (11 hours left to apply)

    Application Process

    Apply directly through Fortrea’s career portal:
    👉 Apply Here

    FAQs

    1. What is the minimum qualification required?
    Bachelor’s in Life Sciences, Pharmacy, Nursing, or related fields. Equivalent experience may also be considered.

    2. Can freshers apply?
    Yes. Fresh graduates with strong academic backgrounds are welcome, provided they meet eligibility criteria.

    3. What is the last date to apply?
    October 11, 2025 (11 hours left to apply)

    4. What does the role involve?
    Processing adverse events, safety reporting, database management, and ensuring compliance with global PV regulations.

    5. Is prior safety experience required?
    Not mandatory. Candidates with up to 2 years of PV or related experience will be considered.

    Quick Summary Table

    Company Fortrea
    Vacancy Safety Science Coordinator I
    Location Bangalore, India
    Required Education BS/BA/MS/MA/PharmD in Life Sciences, Pharmacy, Nursing, Medical Sciences
    Experience 0–2 years in PV, safety, or related fields
    Employment Type Full-time, Office-based
    Salary Competitive with benefits
    Apply By October 11, 2025 (11 hours left to apply)
    Apply Link Fortrea Careers Portal

  • Fortrea Apprentice RFI – STEM & Healthcare

    Fortrea Apprentice RFI – STEM & Healthcare Careers

    Meta Description: Apply for Fortrea Apprentice RFI in Bangalore. STEM/Bachelor grads eligible. Full-time hybrid program with hands-on clinical research exposure.

    Fortrea is opening doors for early-career professionals with its India Apprentice Program. If you are a STEM or Business student eager to kickstart your career in healthcare innovation and clinical research, this is your opportunity. Join a global team that celebrates curiosity, fresh ideas, and the drive to make a real-world impact.

    Company Overview

    Fortrea is a leading global healthcare organization committed to bringing life-changing medicines to patients faster. The company prioritizes innovation, early talent development, and continuous learning. Through structured training, mentorship, and hands-on projects, Fortrea empowers apprentices to gain meaningful experience while contributing to real-world solutions in clinical research and healthcare.

    Job Role & Responsibilities

    As an Apprentice in the RFI Team, you will:

    • Participate in entry-level department functions following Fortrea and sponsor SOPs.
    • Support content updates and assign metadata in the Responsive content library.
    • Assist in content edits and addition of new library material.
    • Contribute to low and mid-complexity Requests for Information (RFIs).
    • Communicate with Subject Matter Experts (SMEs) and internal/external stakeholders.
    • Support Requests for Proposal (RFP) content when required.
    • Execute process-driven tasks ensuring quality and timeliness.

    Eligibility / Qualifications

    • Bachelor’s degree in Science, Technology, or related field.
    • Proven experience managing multiple projects in academic or professional settings.
    • Strong collaboration skills to work with internal and external colleagues.
    • Embraces diverse perspectives and encourages partnership-driven solutions.
    • Excellent customer service, attention to detail, and tactful persistence.
    • Proficiency in MS Office (Excel, Word, Outlook).
    • Ability to plan, multi-task, and prioritize effectively.
    • Strong communication (written and verbal), teamwork, and organizational skills.
    • Analytical mindset with a positive attitude and sense of urgency.
    • Flexibility to work irregular or extended hours to meet client deadlines.

    Relevant Courses:

    B.Sc., B.Tech, B.E., BCA, B.Pharm, Life Sciences, Biotechnology, Biomedical Science, Pharmacy, Healthcare Management

    Location & Salary

    • Location: Bangalore, India
    • Work Type: Full-time, Hybrid
    • Salary: Not specified
    Fortrea Apprentice RFI – STEM & Healthcare
    Fortrea Apprentice RFI – STEM & Healthcare

    Application Process

    Interested candidates can apply directly through Fortrea’s official job portal: Apply Here. Apply early to secure your spot in this competitive program!

    Why Join Fortrea Apprentice Program?

    • Hands-on experience in clinical research, early-phase trials, and market access.
    • Mentorship from experienced professionals.
    • Structured training to accelerate career growth.
    • Exposure to global healthcare operations and cross-functional collaboration.
    • Opportunity to contribute to projects that improve patient outcomes worldwide.

    FAQs

    Q1: Who is eligible for this apprenticeship?
    A1: Bachelor’s degree holders in Science, Technology, or related fields with project experience in academic or professional settings.

    Q2: What is the work location and type?
    A2: The role is hybrid in Bangalore, India, full-time.

    Q3: What skills are required?
    A3: MS Office proficiency, analytical thinking, communication, teamwork, planning, and multitasking abilities.

    Q4: How do I apply?
    A4: Apply via Fortrea’s official portal: Click Here

    Q5: Are there any training opportunities?
    A5: Yes, the program provides structured training and mentorship to help build professional and scientific skills.

    Q6: Is prior experience required?
    A6: Not mandatory, but experience managing multiple projects is beneficial.

    **Q7: What are the growth opportunitie

  • Ardent Clinical Research Hiring – Project Manager, CRA, CTA, Developer

    Ardent Clinical Research Hiring

    Ardent Clinical Research Services hiring Project Manager, CRA, CTA, .NET/Full Stack Developer. Multiple vacancies. Apply now!

    Ardent Clinical Research Services (ACRS), a leading name in clinical research, is expanding its dynamic team. If you’re passionate about advancing healthcare and clinical research, this is your chance to join an organization committed to excellence, innovation, and professional growth. We are seeking talented individuals across multiple roles, from project management to clinical operations and software development.

    Company Overview

    Ardent Clinical Research Services (ACRS) is a renowned clinical research organization (CRO) that delivers high-quality services across global clinical trials. With a strong commitment to advancing healthcare, ACRS offers end-to-end solutions from clinical trial design, project management, site monitoring, and regulatory compliance to data management and software solutions. Known for its industry credibility, ACRS provides employees with an opportunity to work on impactful projects, contribute to medical advancements, and grow in a collaborative environment.

    Job Roles & Responsibilities

    1. Project Manager – Clinical Research

    • Lead and manage clinical research projects ensuring adherence to timelines and budgets.
    • Coordinate cross-functional teams, including clinical operations, regulatory, and data management.
    • Manage client interactions, address project risks, and provide strategic solutions.
    • Ensure compliance with ICH-GCP guidelines and regulatory standards.
    • Mentor team members and support their professional development.

    2. .NET / Full Stack Developer

    • Develop and maintain .NET applications including C#, .NET Core, and Web API.
    • Design, implement, and maintain robust SQL databases.
    • Work on front-end development using React and integrate with cloud platforms (AWS/Azure).
    • Collaborate with cross-functional teams to deliver scalable software solutions.
    • Debug, optimize, and improve existing applications for efficiency.

    3. Clinical Research Associate (CRA)

    • Conduct on-site monitoring visits including initiation, interim, and close-out visits.
    • Ensure adherence to ICH-GCP guidelines and regulatory requirements.
    • Review and manage clinical trial documentation.
    • Communicate effectively with site staff, sponsors, and internal teams.
    • Identify and resolve issues during trial execution.

    4. Clinical Trial Assistant (CTA)

    • Support clinical operations by managing trial documentation and tracking progress.
    • Coordinate with CRAs, sites, and internal teams for smooth trial conduct.
    • Maintain regulatory files and trial master files as per SOPs.
    • Assist in organizing meetings, reports, and communications.
    • Ensure compliance with clinical research standards.

    Eligibility / Qualifications

    • Project Manager – Clinical Research: M.Pharm, B.Pharm, or Life Sciences background; 7+ years in clinical research with 3+ years in project management.
    • .NET / Full Stack Developer: B.Tech / M.Tech in Computer Science or related fields; 4–6+ years in .NET development.
    • Clinical Research Associate (CRA): B.Sc, B.Pharm, M.Pharm, Life Sciences; 2–5 years of on-site monitoring experience.
    • Clinical Trial Assistant (CTA): B.Sc, B.Pharm, Life Sciences; 1–3 years of clinical research support experience.
    • Knowledge of ICH-GCP, regulatory standards, project management tools, and software development best practices.

    Relevant Courses: M.Pharm, B.Pharm, B.Sc Life Sciences, M.Tech Computer Science, B.Tech Computer Science, Clinical Research Certification, Project Management Certification.

    Location & Salary

    • Location: Bengaluru, India.
    • Salary: Competitive and commensurate with experience (details provided during the interview process).

    Application Process

    Interested candidates are encouraged to send their updated resume to 👉 hr@ardent-cro.com before the positions are filled. Act quickly to secure your spot in this leading clinical research organization!

    FAQs

    Q: What is the application deadline?
    A: Applications are accepted on a rolling basis until positions are filled. Apply promptly to ensure consideration.

    Q: Are freshers eligible?
    A: CTA and junior developer roles may consider candidates with relevant internships or 1–2 years of experience.

    Q: What is the interview process?
    A: Candidates may undergo a multi-stage interview including HR screening, technical/role-specific evaluation, and final discussion with department heads.

    Q: What career growth opportunities exist?
    A: ACRS offers structured career development programs, mentorship, and opportunities to work on global clinical trials.

    Q: Can I work remotely?
    A: The roles primarily require on-site presence in Bengaluru due to project and clinical site coordination needs.

    Q: What benefits does ACRS provide?
    A: Benefits include competitive salary, health insurance, professional development programs, and a collaborative work environment.

    Category Details
    Company Ardent Clinical Research Services (ACRS)
    Vacancies Project Manager – Clinical Research, .NET/Full Stack Developer, CRA, CTA
    Required Education M.Pharm, B.Pharm, B.Sc Life Sciences, M.Tech Computer Science, B.Tech Computer Science, Clinical Research Certification, Project Management Certification
    Experience Project Manager: 7+ yrs (3+ in management), .NET Developer: 4–6+ yrs, CRA: 2–5 yrs, CTA: 1–3 yrs

  • Labcorp Fresher Hiring Technical Reporting Associate

    Technical Reporting Associate Vacancy – Labcorp Bangalore

    Apply for Labcorp Technical Reporting Associate I in Bangalore. Openings for M.Sc, B.Pharm, M.Pharm, M.Tech, B.Tech (Biotech) freshers with 0-6 months exp.

    Labcorp, a global leader in life sciences and clinical research, is inviting applications for the position of Technical Reporting Associate I at its Bangalore location. This is an excellent opportunity for fresh graduates and early-career professionals to build a career in scientific data reporting, clinical research documentation, and non-clinical study support within one of the world’s most respected pharma research organizations.

    Company Overview

    Labcorp is a leading global life sciences company with nearly 70,000 employees across more than 100 countries. Renowned for its innovation in diagnostics and drug development, Labcorp plays a crucial role in accelerating healthcare decisions, advancing medical research, and improving patient outcomes. With state-of-the-art technology, scientific expertise, and an inclusive work culture, Labcorp is recognized as a trusted partner for hospitals, pharmaceutical companies, and healthcare providers worldwide.

    Job Role & Responsibilities

    As a Technical Reporting Associate I, you will be part of the Global Reporting Solutions team. This role focuses on learning, developing, and supporting non-clinical study reports. Key responsibilities include:

    • Learning and using advanced software tools for word processing, spreadsheets, data tables, and collaboration platforms.
    • Preparing accurate data tables from study protocols, including basic statistical analysis using reporting tools like ToxReporting.
    • Drafting and quality-checking data tables, CTD tabulated summaries, and manually prepared reports.
    • Performing QC activities to ensure high-quality deliverables.
    • Managing a full study workload post-training, with varying study designs.
    • Providing peer review of colleagues’ work and mentoring junior team members after gaining proficiency.
    • Collaborating with supervisors and global teams to resolve delivery challenges.

    This role ensures compliance with global regulatory requirements and prepares you for a future career in regulatory writing, medical writing, pharmacovigilance, and clinical research documentation.

    Eligibility / Qualifications

    Labcorp is looking for science graduates with a keen interest in research reporting and scientific documentation. The eligibility criteria include:

    • Education: M.Sc (Life Sciences, Biotechnology, Biochemistry, Microbiology, Zoology, Chemistry), B.Pharm, M.Pharm, B.Tech (Biotechnology), M.Tech (Biotechnology)
    • Experience: 0–6 months (Freshers encouraged to apply)
    • Skills Required:
      • Strong attention to detail and accuracy in reporting.
      • Knowledge of MS Office tools (Word, Excel, PowerPoint).
      • Basic understanding of study design, data entry, and reporting.
      • Good written and verbal communication skills.
      • Ability to work in a team and meet project deadlines.

    Location & Salary

    • Location: Bangalore, India
    • Job Type: Full-time, entry-level position
    • Work Environment: Collaborative, global reporting solutions team
    • Salary: Competitive (as per industry standards for freshers)
    Labcorp Fresher Hiring Technical Reporting Associate Vacancy
    Labcorp Fresher Hiring Technical Reporting Associate Vacancy

    Application Process

    Interested candidates can apply directly through the official Labcorp career portal. Ensure your resume highlights your academic qualifications, research projects, and technical skills.

    👉 Click here to apply now

    Deadline: October 10, 2025 (Apply before the closing date to secure your application).

    Why Join Labcorp?

    • Work with a global leader in clinical research and diagnostics.
    • Gain hands-on exposure to non-clinical study reporting and regulatory documentation.
    • Benefit from mentorship, structured training, and knowledge-sharing.
    • Opportunity to grow into roles like Regulatory Writer, Clinical Data Analyst, or Pharmacovigilance Specialist.
    • Be part of an inclusive, diverse workplace committed to equal opportunity.

    FAQs

    1. Who can apply for Labcorp’s Technical Reporting Associate I role?
    Candidates with M.Sc, B.Pharm, M.Pharm, B.Tech (Biotech), M.Tech (Biotech) and 0–6 months of experience are eligible.

    2. Is this job open for freshers?
    Yes, fresh graduates in life sciences, pharmacy, and biotechnology are encouraged to apply.

    3. What skills are required?
    Attention to detail, proficiency in MS Office, basic knowledge of study design, and good communication skills.

    4. What is the location of this job?
    The role is based in Bangalore, India.

    5. What is the deadline to apply?
    The last date to apply is October 10, 2025.

    6. Does Labcorp provide equal opportunities?
    Yes, Labcorp is an Equal Opportunity Employer and promotes inclusion, diversity, and fairness in all hiring decisions.

    Summary Table

    Company Labcorp
    Vacancies Technical Reporting Associate I
    Required Education M.Sc, B.Pharm, M.Pharm, B.Tech (Biotech), M.Tech (Biotech)
    Experience 0–6 Months
    Location Bangalore, India
    Deadline October 10, 2025

  • Executive Production Vacancy – Apotex

    Executive Production Vacancy – Apotex | M.Pharm/Pharma | Bangalore

    Apply now for Executive Production at Apotex, Bangalore. Openings for B.Pharm/M.Pharm with 3–5 years’ experience in pharma manufacturing.

    Apotex, a Canadian-based global pharmaceutical leader, is inviting applications for the role of Executive, Production at its Bangalore facility. This position is ideal for professionals with a strong background in pharmaceutical production who are passionate about quality, compliance, and teamwork. If you hold a B.Pharm or M.Pharm degree with 3–5 years of industry experience, this is your chance to grow your career with one of the largest Canadian-based pharmaceutical companies.

    Company Overview

    Apotex Inc. is a trusted name in the pharmaceutical industry, headquartered in Toronto, Canada, with global offices across the United States, Mexico, and India. With a robust portfolio of generic medicines, biosimilars, innovative branded pharmaceuticals, and consumer health products, Apotex is committed to improving everyday access to affordable healthcare worldwide.

    Job Role & Responsibilities

    As an Executive, Production, you will be responsible for supervising and ensuring efficient, compliant, and timely production processes. Your key duties include:

    • Supervising packaging and production activities with adherence to cGMP and SOPs.

    • Ensuring safety, cleanliness, and housekeeping practices in the production department.

    • Performing batch documentation, labeling, and online records as per compliance standards.

    • Overseeing equipment calibration, preventive maintenance, and cleaning validation activities.

    • Training operators, contract labor, and new staff on SOPs, GMP, and documentation practices.

    • Planning and executing production activities to meet weekly and daily schedules.

    • Supervising process validation and ensuring compliance with QA/QC standards.

    • Escalating deviations, non-compliances, or abnormal observations to superiors immediately.

    • Collaborating with cross-functional departments to ensure smooth operations.

    • Demonstrating company values – Collaboration, Courage, Perseverance, and Passion – in daily work.

    Eligibility / Qualifications

    • Education: B.Pharm / M.Pharm

    • Experience: 3–5 years in pharmaceutical production or packaging operations.

    • Skills Required:

      • Strong knowledge of cGMP practices

      • Ability to handle and supervise packaging activities

      • Proficiency in documentation and compliance requirements

      • Effective team collaboration and problem-solving

    Executive Production Vacancy – Apotex | M.Pharm/Pharma | Bangalore
    Executive Production Vacancy – Apotex | M.Pharm/Pharma | Bangalore

    Location & Salary

    • Location: Bangalore, Karnataka, India – 560099

    • Salary: As per industry standards (not disclosed in posting).

    Application Process

    Interested candidates can apply directly through the Apotex careers portal:

    👉 Apply Here

    Why Join Apotex?

    • Work with one of the largest Canadian-based pharmaceutical companies.

    • Exposure to global best practices in manufacturing, compliance, and quality standards.

    • Opportunities for professional growth and cross-functional collaboration.

    • Supportive work culture fostering employee development and accessibility.

    FAQs

    Q1. What qualification is required for this role?
    B.Pharm or M.Pharm degree in Pharmaceutical Sciences is required.

    Q2. How many years of experience are needed?
    Applicants should have 3–5 years of experience in production or packaging activities.

    Q3. Is this role open for freshers?
    No, this position requires prior experience in pharmaceutical production.

    Q4. Where is the job location?
    The role is based in Bangalore, Karnataka (560099).

    Q5. How do I apply?
    Submit your application via the official Apotex career link provided above.

    Summary Table

    Company Apotex Inc.
    Vacancies Executive, Production
    Required Education B.Pharm, M.Pharm
    Experience 3–5 years
    Location Bangalore, Karnataka, India (560099)

  • IQVIA Hiring Clinical Data Management Professionals

    Clinical Data Management Lead | B.Pharm | IQVIA | India

    Apply for Clinical Data Management Lead at IQVIA, India. B.Pharm/Biotech, 2–6 yrs experience. Hybrid locations: Bangalore, Kochi, Kolkata.

    Advance Your Career in Clinical Data Management with IQVIA

    IQVIA, a global leader in clinical research services, commercial insights, and healthcare intelligence, is inviting talented professionals to join our Clinical Data Management team. We are seeking skilled individuals who are passionate about delivering high-quality data management services and driving innovative solutions in clinical research. If you have hands-on experience in Core Data Management and are looking for an opportunity to work in a collaborative, hybrid environment, this is your chance to grow your career with a trusted industry leader.

    Company Overview

    IQVIA is a premier global provider of healthcare intelligence, clinical research services, and commercial insights. With a presence across multiple continents, we accelerate the development and commercialization of innovative medical treatments, helping improve patient outcomes worldwide. Our expertise combines advanced analytics, technology, and domain knowledge to deliver intelligent solutions that drive healthcare forward.

    Why Join IQVIA?

    • Work with a globally recognized leader in clinical research and data management.

    • Contribute to advancing medical treatments and improving patient health.

    • Collaborate with multidisciplinary teams in a dynamic, hybrid work environment.

    • Access comprehensive training programs and career growth opportunities.

    Job Role & Responsibilities

    As a Clinical Data Management Lead (CDM Project Lead), you will play a pivotal role in delivering end-to-end data management services across clinical studies. Your responsibilities include:. corinna

    • Managing the delivery of data management services for single or multi-service projects, ensuring timelines, budgets, and quality standards are met.

    • Leading project planning, execution, and close-out activities for assigned studies.

    • Coordinating study set-up requirements and validating new device integrations.

    • Performing regular data cleaning activities to ensure data integrity and timely sponsor deliverables.

    • Overseeing the implementation of database revisions and new technologies.

    • Leading internal study meetings, sponsor audits, and study kick-off sessions.

    • Training new joiners and mentoring junior team members.

    • Reviewing and updating standard operating procedures and working instructions.

    • Maintaining effective communication with line managers, project teams, and cross-functional stakeholders.

    Key Skills & Competencies:

    • Expertise in Rave EDC and other clinical data management systems.

    • Strong understanding of the drug development lifecycle and clinical research processes.

    • Proficiency in Microsoft Excel, Word, Outlook, and other advanced computer applications.

    • Leadership, team collaboration, and project management capabilities.

    Eligibility / Qualifications

    • Bachelor’s Degree in Pharmacy, Life Sciences, or related fields (B.Pharm, B.Sc., Biotechnology).

    • 2–6 years of relevant experience in clinical data management.

    • Minimum 1 year as a CDM Project Lead preferred.

    • Fluent in English, both written and spoken.

    • Strong analytical, organizational, and communication skills.

    Relevant Courses: B.Pharm, M.Pharm, B.Sc Biotechnology, M.Sc Biotechnology, Clinical Research, Life Sciences

    Location & Work Model

    • Work Locations: Bangalore | Kochi | Kolkata

    • Work Model: Hybrid (office + remote flexibility)

    • Employment Type: Full-time, Regular

    IQVIA Hiring Clinical Data Management Professionals
    IQVIA Hiring Clinical Data Management Professionals

    Application Process

    Interested candidates can apply directly through the IQVIA career portal or by sending a resume via email:

    CTA: Apply today to be part of a world-class data management team and drive healthcare innovation! Don’t miss this opportunity—submit your application before the deadline.

    FAQs

    Q1: Can freshers apply for this role?
    A1: This position requires 2–6 years of experience in Core Data Management. Freshers are not eligible.

    Q2: What are the work locations?
    A2: The role offers hybrid work options across Bangalore, Kochi, and Kolkata.

    Q3: What qualifications are required?
    A3: A Bachelor’s degree in Pharmacy, Biotechnology, Life Sciences, or equivalent is required. M.Sc. or relevant postgraduate degrees are preferred.

    Q4: How to apply for the role?
    A4: Candidates can apply via the IQVIA career portal or email their CV directly to vaishnavinandkishor.kamble@iqvia.com.

    Q5: Is training provided for new joiners?
    A5: Yes, IQVIA provides onboarding and continuous training to support career growth and skill development.

    Vertical Summary Table

    Category Details
    Company IQVIA
    Vacancies Clinical Data Management Lead (Multiple Openings)
    Required Education B.Pharm, B.Sc Biotechnology, M.Sc Biotechnology, Life Sciences, Clinical Research
    Experience 2–6 years in Core Data Management, 1 year as CDM Project Lead preferred