Job Tag: Pharma Jobs in Bangalore

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Clinical Data Associate II Vacancy | Trialmed PPD Clinical Research Bangalore

Apply for Clinical Data Associate II at Trialmed (PPD, Thermo Fisher Scientific), Bangalore. Openings for graduates with 2+ years’ data management experience.

Trialmed, a global site network and the early phase clinical solution for PPD® clinical research, part of Thermo Fisher Scientific Inc., is hiring for the role of Clinical Data Associate II (CDA) in Bangalore, India. This fully remote role provides an exceptional opportunity to join a leading global contract research organization (CRO) dedicated to accelerating drug development and bringing cures to market.

Company Overview

Thermo Fisher Scientific

is a world leader in serving science, with the mission to make the world healthier, cleaner, and safer. Through its PPD clinical research division, Thermo Fisher advances clinical trial data management and operations on a global scale. Trialmed, as part of PPD, powers early phase clinical research with cutting-edge data-driven solutions. Joining this team means contributing directly to innovative drug development and patient health worldwide.

Job Role & Responsibilities

As a Clinical Data Associate II, you will be responsible for managing critical aspects of clinical trial data, ensuring accuracy, compliance, and regulatory alignment. Your responsibilities include:

• Identifying and resolving data discrepancies and updating clinical databases.
• Generating, tracking, and resolving data clarifications and queries.
• Reviewing data listings for accuracy, consistency, and regulatory compliance.
• Producing regular status reports for CDM management and sponsors.
• Managing Serious Adverse Event (SAE) and Third-Party Vendor data reconciliations.
• Performing advanced data cleaning processes to ensure patient safety and efficacy analysis.
• Working independently on complex assignments requiring critical thinking and innovation.
• Contributing to CRF (Case Report Form) design and database development.
• Facilitating effective communication with internal teams, sponsors, and global partners.

Eligibility / Qualifications

• Education: Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, Clinical Research, or related fields.
• Experience:
  • Minimum 2+ years of data management or related experience.
  • Hands-on expertise with clinical trial data management tools.
• Skills:
  • Proficiency with Medidata Rave, Veeva Vault, and EDC databases.
  • Strong knowledge of GCP, eTMF, and data validation processes.
  • Excellent written and verbal communication in English.
  • Strong analytical, problem-solving, and documentation skills.
  • Ability to manage projects independently with minimal supervision.
  • Adaptability to global teams, diverse cultures, and dynamic environments.

Location & Salary

• Job Location: Bangalore, Karnataka, India (remote opportunity).
• Work Mode: Fully remote / Hybrid / Office (flexible).
• Work Schedule: 1:00 PM to 10:00 PM IST (Second Shift).
• Salary: Competitive, based on experience and qualifications.

Application Process

Candidates interested in joining the global PPD/Trialmed team can apply through the official Thermo Fisher Scientific careers portal: Apply Here

Apply early to maximize your chance of being shortlisted!

FAQs

1. Who is eligible to apply?

Graduates in Life Sciences, Pharmacy, Biotechnology, or related fields with at least 2 years’ data management experience.

2. Is prior experience with EDC tools required?
Yes, experience with Medidata Rave, Veeva Vault, or similar EDC systems is preferred.

3. Can this role be performed remotely?
Yes, this position offers remote, hybrid, and office work options.

4. What is the standard work schedule?
The role requires working second shift hours (1:00 PM – 10:00 PM IST).

5. What is the career growth potential?
Clinical Data Associates at Trialmed gain exposure to global projects, cutting-edge data technologies, and career progression in clinical data management.

Career Benefits at Trialmed (PPD/Thermo Fisher Scientific)

• Be part of a leading global CRO shaping the future of clinical research.
• Exposure to international data management standards and regulatory compliance.
• Career growth in clinical trials, data management, and biostatistics.
• Flexibility to work remotely, enabling better work-life balance.
• Access to training, global networking, and advanced digital tools.

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Safety Science Coordinator II – Fortrea (2–3 Years Experience, Bangalore)

Safety Science Coordinator II – Pharma, 2-3 Yrs, Bangalore
Apply for Safety Science Coordinator II at Fortrea, Bangalore. Pharma/Life Sciences graduates with 2–3 years drug safety experience.

Looking for an exciting opportunity in drug safety and pharmacovigilance? Fortrea is inviting applications for the role of Safety Science Coordinator II at its Bangalore location. This position is ideal for professionals with 2–3 years of experience in pharmacovigilance or clinical trial case processing who are eager to contribute to global clinical safety operations.

Company Overview

Fortrea is a global leader in clinical research and drug development services, working closely with pharmaceutical and biotechnology organizations worldwide. With a mission to deliver safer and more effective therapies, Fortrea is recognized for its innovation, regulatory expertise, and dedication to advancing healthcare.

As a trusted partner in the life sciences industry, Fortrea provides end-to-end support in clinical development, patient safety, and data-driven insights—helping shape the future of drug safety and pharmacovigilance.

Job Role & Responsibilities

As a Safety Science Coordinator II, you will be responsible for ensuring compliance and quality in pharmacovigilance and clinical safety operations. Your role will involve:

• Adverse Event Case Processing

  • Receipt, review, and entry of AE/SAE reports from clinical trials or spontaneous sources.

  • Writing patient narratives and coding adverse events using MedDRA.

  • Identifying missing or clinically significant data and generating queries for collection.

• Regulatory Submissions & Reporting

  • Submitting expedited SAE reports to clients, regulatory authorities, ethics committees, and investigators.

  • Managing Expedited Safety Reports (ESRs) and Periodic Safety Reports (PSRs).

  • Ensuring timelines for safety submissions are strictly met.

• Quality Management & Documentation

  • Maintaining project files, central documentation, and adverse event tracking systems.

  • Supporting database reconciliation and quality review of processed reports.

  • Assisting in preparation for audits and regulatory inspections.

• Training & Collaboration

  • Mentoring junior pharmacovigilance staff.

  • Coordinating with internal stakeholders, clients, and regulatory agencies.

  • Participating in client meetings and contributing to project metrics and monthly reports.

Eligibility / Qualifications

Essential:

• Bachelor’s or Master’s degree in Pharmacy, Biological Sciences, Nursing, Medical Sciences, Life Sciences, or related fields.

• 2–3 years of drug safety experience with exposure to clinical trial case processing.

Desirable Skills:

• High accuracy and attention to detail in pharmacovigilance case handling.

• Strong knowledge of MS Office and safety databases.

• Excellent written and verbal communication skills.

• Ability to work independently with minimal supervision.

• Mentoring and leadership skills are a plus.

Location & Salary

• Location: Bangalore, India

• Work Mode: Hybrid (office environment with flexibility)

• Compensation: Competitive salary with benefits aligned to global CRO industry standards

Application Process

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

📅 Application Deadline: 28 September 2025

Why Join Fortrea?

• Be part of a global leader in clinical safety and drug development.

• Work on cutting-edge projects ensuring patient safety across markets.

• Gain exposure to international pharmacovigilance regulations and practices.

• Grow your career with continuous learning, mentoring, and professional development.

FAQs

Q1: Who can apply for this position?
Candidates with a degree in Pharmacy, Life Sciences, Medical Sciences, or Nursing and at least 2–3 years of pharmacovigilance/drug safety experience can apply.

Q2: What kind of work environment does Fortrea offer?
Fortrea offers a hybrid work model with an office base in Bangalore, ensuring both flexibility and team collaboration.

Q3: Is prior clinical trial experience mandatory?
Yes, exposure to clinical trial case processing is required for this role.

Q4: What software skills are needed?
Working knowledge of pharmacovigilance databases, MedDRA coding, and MS Office tools is required.

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Drug Safety Associate I | Qinecsa | Mysore & Bangalore

Apply now for Drug Safety Associate I role at Qinecsa. Hybrid work model, 1+ year PV experience, B.Pharm/M.Pharm/Pharm.D required. Immediate joiners!

Qinecsa, a trusted leader in pharmacovigilance and drug safety solutions, is hiring for the role of Drug Safety Associate I. This hybrid position offers candidates an exciting opportunity to begin their journey with a global team focused on patient safety and regulatory compliance.

Company Overview

Qinecsa is dedicated to ensuring patient safety and compliance with global pharmacovigilance standards. With cutting-edge technology, a strong focus on quality, and a mission-driven culture, Qinecsa supports life sciences organizations in delivering safe and effective therapies. Joining Qinecsa means contributing to a team that is committed to improving healthcare outcomes worldwide.

Job Role & Responsibilities

As a Drug Safety Associate I, your responsibilities include:

• Performing case processing of adverse events in compliance with regulatory timelines and quality standards.
• Ensuring accurate data entry and narrative writing for pharmacovigilance reports.
• Supporting safety signal detection and regulatory submissions.
• Collaborating with cross-functional teams to maintain compliance and quality.
• Contributing to the development of standard operating procedures (SOPs) and best practices.

Eligibility / Qualifications

• Education: B.Pharm, M.Pharm, or Pharm.D from a recognized university.
• License: Must hold a valid Pharmacy License.
• Experience: Minimum 1 year of pharmacovigilance experience.
• Skills:
  • Strong attention to detail and accuracy.
  • Good communication and teamwork abilities.
  • Knowledge of PV databases and global reporting guidelines.

Location & Work Type

• Job Location: Hybrid – Mysore/Bangalore
• Work Mode: Initial 6 months work-from-home; relocation required after probation.
• Start Date: Immediate joiners only.

Compensation & Benefits

• Competitive salary package based on qualifications and experience.
• Exposure to global pharmacovigilance practices.
• Career growth opportunities in drug safety and regulatory sciences.
• Hybrid work flexibility with structured training and onboarding support.

Application Process

Interested candidates should email their updated CV to:
📧 nithin.vijendra@qinecsa.com
Subject line format: Name_Drug Safety Associate I_Notice Period

Apply today to accelerate your pharmacovigilance career with Qinecsa!

FAQs

1. Who can apply for this position?
Candidates with B.Pharm, M.Pharm, or Pharm.D and a valid pharmacy license, along with at least 1 year of pharmacovigilance experience.

2. Is remote work allowed?
Yes. The role offers 6 months work-from-home before relocation to Mysore/Bangalore.

3. What is the notice period requirement?
Only immediate joiners will be considered.

4. What kind of career growth can I expect?
Qinecsa provides structured learning, global exposure, and opportunities for advancement in drug safety and regulatory affairs.

5. How can I apply?
Send your CV to nithin.vijendra@qinecsa.com with the subject line format mentioned above.

Quick Summary Table

Infosys Hiring Regulatory & Clinical Business Analyst – Bangalore

Infosys Limited hiring Regulatory & Clinical Business Analyst in Bangalore. Apply with 3–15 years’ experience in life sciences or regulatory IT solutions.

Infosys Limited, a global leader in consulting, technology, and outsourcing, is inviting applications for the position of Regulatory and Clinical Business Analyst in Bangalore, India. This is a full-time opportunity for professionals with IT and life sciences expertise to contribute to regulatory compliance, clinical trial solutions, and pharmacovigilance technology systems.

Company Overview

Infosys is a world-renowned IT and consulting firm, recognized for driving digital transformation and delivering high-value solutions across industries. In the Life Sciences domain, Infosys partners with global pharmaceutical, biotechnology, and healthcare clients to build technology-driven solutions for clinical trials, drug safety, pharmacovigilance, and regulatory compliance. With a strong focus on innovation, Infosys empowers its employees to collaborate with global clients and design impactful strategies.

Job Role & Responsibilities

As a Regulatory and Clinical Business Analyst, your role will involve:

• Leading projects in Clinical or Regulatory IT solutions for Life Sciences clients.
• Collaborating with SMEs, development teams, and client teams across the project lifecycle.
• Utilizing expertise in clinical trials, drug safety, and pharmacovigilance systems.
• Working with CSV tools and regulatory compliance systems.
• Developing value-creating strategies to help clients innovate and improve profitability.
• Contributing to software configuration management and technology solution design.
• Identifying process improvement opportunities and recommending innovative IT solutions.
• Managing project teams and financial processes effectively.

Eligibility / Qualifications

• Education: Bachelor of Engineering, Bachelor of Technology, BCA, B.Pharm, M.Pharm, MCA, M.Tech.
• Experience: 3–15 years total IT experience, with at least 3 years in Clinical or Regulatory solutions for Life Sciences.
• Essential Skills:
  • Life Sciences domain knowledge (Clinical Trials, Drug Safety, Pharmacovigilance).
  • Familiarity with CSV tools and US Life Sciences market.
  • Client interfacing and project management skills.
  • Strong logical thinking, problem-solving, and collaboration abilities.
• Preferred Skills:
  • Clinical Trials domain knowledge.
  • Regulatory compliance systems expertise.
  • Awareness of emerging technologies and industry trends.

Relevant courses under eligibility: B.Pharm, M.Pharm (Regulatory Affairs/Clinical Research), B.Tech/M.Tech Biotechnology, MCA, BCA, Life Sciences IT specialization.

Location & Salary

• Location: Bangalore, India
• Work Model: Full-time (onsite with client interfacing responsibilities)
• Compensation: Competitive salary as per Infosys pay scales and industry standards
• Service Line: Application Development and Maintenance

Application Process

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

Why Join Infosys?

• Work with a global IT leader on regulatory and clinical solutions for top life sciences clients.
• Gain exposure to cutting-edge compliance technologies and US Life Sciences market.
• Collaborate with global SMEs and client stakeholders across domains.
• Access structured career growth opportunities in pharma IT solutions.
• Be part of an organization recognized for innovation, integrity, and inclusion.

FAQs

Q1: What qualifications are required for this role?
Engineering, Technology, Pharmacy, Computer Applications (BCA/MCA), or related life sciences degrees.

Q2: How much experience is needed?
3–15 years total IT industry experience, with 3+ years in Clinical/Regulatory solutions.

Q3: What skills are most important?
Domain expertise in clinical trials, pharmacovigilance, CSV tools, client management, and regulatory compliance systems.

Q4: Where is the role based?
At Infosys Limited, Bangalore.

Q5: How do I apply?
Applications can be submitted through Infosys’s official career portal (link above).

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Novartis Hiring Clinical Trial Associate – Apply Now India

Novartis seeks Clinical Trial Associates in India. Apply with 1+ years’ clinical operations experience. Full-time role in global pharma.

Novartis, one of the world’s leading pharmaceutical companies, is hiring for the role of Clinical Trial Associate (CTA) in India. This is a full-time opportunity for candidates with experience in clinical operations and trial management, offering the chance to work in a global healthcare leader committed to innovation and patient safety.

Company Overview

Novartis is reimagining medicine to improve and extend people’s lives. With a mission to become the most valued and trusted medicines company, Novartis continues to pioneer cutting-edge therapies across multiple therapeutic areas. Operating worldwide, the company is recognized for its scientific innovation, commitment to diversity, and dedication to patient communities. Employees at Novartis benefit from a supportive work culture, professional growth opportunities, and a strong focus on work-life balance.

Job Role & Responsibilities

As a Clinical Trial Associate, you will play a key role in supporting clinical study setup and execution. Your responsibilities include:

• Supporting document collection, preparation, and submission to IRB/EC and Health Authorities.
• Assisting with vendor selection, third-party risk management (TPRM), and trial management file (TMF) setup and maintenance.
• Ensuring site “Green Light” readiness for drug release in collaboration with Qualified Persons.
• Preparing and translating informed consent forms (ICF) into local languages.
• Managing patient-facing materials and archiving clinical trial documents.
• Supporting Study Start-Up (SSU) strategy, ensuring adherence to deliverables and country-specific commitments.
• Coordinating financial standards, logistics, and compliance with ICH/GCP, SOPs, and health authority regulations.
• Collaborating with clinical research associates (CRAs), clinical project managers (CPMs), and SSU managers across trial phases.
• Implementing innovative and efficient trial processes aligned with Novartis strategies.

Eligibility / Qualifications

• Education: Bachelor’s degree (vocational qualification, commercial/medical training, or equivalent). Preferably trained as a medical records administrator or with similar education.
• Experience: 1+ years in clinical operations with trial setup and contracting exposure.
• Technical Skills:
  • Proficiency in MS Excel, MS Word, and MS PowerPoint; SAP knowledge preferred.
  • Strong understanding of drug development, trial setup, and regulatory processes.
  • Knowledge of international drug development standards (ICH/GCP, FDA, EMA, Health Authorities).
• Soft Skills:
  • Strong organizational and prioritization skills.
  • Ability to collaborate effectively across functions.
  • Self-motivated, structured, and detail-oriented.

Relevant courses under eligibility: B.Sc/M.Sc Life Sciences, B.Pharm, M.Pharm, Clinical Research, Biotechnology, Biochemistry, Medical Records Administration.

Location & Salary

• Location: India (specific office details to be provided upon selection)
• Work Model: Full-time, with possible travel to field sites
• Compensation: Competitive salary and benefits, as per Novartis standards
• Additional Benefits: Refer to the Novartis Life Handbook for rewards and employee benefits.

Application Process

Interested candidates can apply directly through Novartis’ official careers portal:
Apply Here

If you require accommodations during the recruitment process, contact: diversityandincl.india@novartis.com with the job requisition ID REQ-10061713.

Why Join Novartis?

• Be part of a company driving innovation in global healthcare.
• Access a supportive and inclusive work culture with career growth opportunities.
• Collaborate with experts in clinical operations and regulatory affairs.
• Contribute to clinical trials that directly impact patient health and safety worldwide.
• Work in a company recognized for diversity, equity, and inclusion.

FAQs

Q1: What qualifications are required for this role?
A bachelor’s degree or equivalent vocational qualification, with preference for candidates with clinical operations experience.

Q2: How much experience is needed?
At least 1+ years in clinical operations, especially in trial setup and regulatory processes.

Q3: What skills are preferred?
Proficiency in MS Office, knowledge of ICH/GCP, FDA, EMA regulations, and SAP familiarity.

Q4: Where is the role based?
The role is based in India, with some travel to field sites as required.

Q5: How do I apply?
Apply directly via the Novartis careers portal (link provided above).

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