PHARMA STUFF

Job Tag: Pharma Jobs in Chennai

  • Pharmacovigilance Freshers – Associate Safety Data Management Specialist | Pfizer

    Freshers – Associate Safety Data Management Specialist | Pfizer Chennai

    Apply for Pfizer’s Associate Safety Data Management Specialist role in Chennai. Freshers (B.Pharm, M.Pharm, Pharm.D) eligible. Hybrid work model.

    In today’s fast-evolving pharmaceutical landscape, Pfizer stands tall as one of the world’s most trusted leaders in healthcare innovation. The company continues to transform patient outcomes through its research-driven approach and commitment to global health excellence. As part of its growing pharmacovigilance team, Pfizer invites fresh pharmacy graduates to apply for the Associate Safety Data Management Specialist position in Chennai, India. This hybrid opportunity allows aspiring professionals to build a strong foundation in drug safety, regulatory compliance, and medical data management within one of the most reputed pharmaceutical organizations worldwide.

    Company Overview

    Pfizer Inc. is a global biopharmaceutical company headquartered in New York, USA, dedicated to delivering breakthroughs that change patients’ lives. With operations in over 125 countries, Pfizer continues to push the boundaries of science and innovation. In India, Pfizer has established its reputation as a top employer in the pharma and life sciences industry—providing a culture of collaboration, inclusivity, and continuous learning.

    Pfizer’s Chennai center plays a pivotal role in supporting global pharmacovigilance, medical writing, regulatory affairs, and clinical operations. The company’s focus on data-driven safety processes ensures that every medicine released meets the highest standards of quality and compliance.

    Job Role & Responsibilities

    As an Associate Safety Data Management Specialist, you will support Pfizer’s global pharmacovigilance (PV) operations by processing and evaluating individual case safety reports (ICSRs) from both clinical trial and post-marketing sources. This is a highly analytical role ideal for detail-oriented professionals passionate about drug safety and patient well-being.

    Key Responsibilities:

    • Perform ICSR case processing activities within the ARGUS Safety Database.
    • Assess case validity and conduct duplicate checks to ensure data integrity.
    • Identify and code adverse events using MedDRA and WHO Drug Dictionaries.
    • Perform causality assessments, seriousness evaluation, and listedness determination as per company SOPs.
    • Draft comprehensive narratives summarizing patient cases.
    • Perform case prioritization and ensure timely case submissions to regulatory authorities.
    • Collaborate with global cross-functional teams for follow-up actions.
    • Maintain 100% compliance with Good Pharmacovigilance Practices (GVP) and company quality systems.
    • Ensure all tasks adhere to Pfizer’s Standard Operating Procedures (SOPs) and global safety standards.

    Eligibility / Qualifications

    Pfizer welcomes fresh graduates passionate about pharmacovigilance and regulatory safety management.

    Minimum Qualifications:

    • Bachelor’s or Master’s degree in Pharmacy (B.Pharm, M.Pharm) or Doctor of Pharmacy (Pharm.D).
    • Strong attention to detail and ability to manage complex datasets.
    • Excellent analytical and written communication skills.
    • Demonstrated teamwork, collaboration, and continuous learning mindset.

    Preferred Qualifications:

    • Certification or course completion in Pharmacovigilance, Drug Safety, or Clinical Research.
    • Familiarity with medical terminology, safety databases, and regulatory frameworks.
    • Publications in peer-reviewed journals will be an added advantage.

    Location & Work Mode

    • Work Location: Chennai, India
    • Work Type: Hybrid (mix of remote and on-site work)

    Pfizer offers a dynamic workplace that values flexibility and supports a hybrid work environment—balancing productivity, collaboration, and employee well-being.

    Salary & Benefits

    While the official salary details are not disclosed, similar entry-level pharmacovigilance roles at Pfizer offer competitive pay packages ranging from ₹4 LPA to ₹6 LPA for freshers, depending on educational background and skills.

    Employee Benefits Include:

    • Hybrid work flexibility
    • Health and wellness coverage
    • Continuous learning programs
    • Global exposure through collaboration with international teams
    • Opportunities for career advancement in PV and regulatory domains
    Pharmacovigilance Freshers – Associate Safety Data Management Specialist - Pfizer
    Pharmacovigilance Freshers – Associate Safety Data Management Specialist – Pfizer

    Application Process

    To apply, visit the official Pfizer career portal using the link below:
    👉 Apply Now at Pfizer Careers

    Why Join Pfizer?

    Pfizer’s mission—Breakthroughs that change patients’ lives—reflects its dedication to transforming healthcare globally. Joining Pfizer as an Associate Safety Data Management Specialist gives you the opportunity to:

    • Build your career in one of the world’s largest and most respected pharmaceutical organizations.
    • Gain hands-on experience in global drug safety and pharmacovigilance systems.
    • Learn from experts who have contributed to some of the most impactful therapies in modern medicine.
    • Be part of a collaborative culture that values innovation, inclusion, and continuous learning.

    FAQs

    1. Is this role open to freshers?
    Yes, Pfizer’s Associate Safety Data Management Specialist role is open to fresh B.Pharm, M.Pharm, and Pharm.D graduates.

    2. Do I need prior experience to apply?
    No prior work experience is required. Candidates with pharmacovigilance certification or internships will have an added advantage.

    3. What is the salary range for this position?
    The estimated salary for freshers ranges between ₹4,00,000 to ₹6,00,000 per annum, depending on qualifications and skills.

    4. Is this a permanent position?
    Yes, it’s a full-time position with Pfizer’s Chennai division.

    5. What is the work model?
    The role follows a hybrid model, allowing partial remote work flexibility.

    6. How can I apply?
    Apply directly via Pfizer’s official career page: Pfizer Careers – Apply Now

    7. What skills are essential for this role?
    Attention to detail, strong analytical ability, good communication, and basic understanding of pharmacovigilance and regulatory terms.

    Summary Table

    Category Details
    Company Pfizer Ltd.
    Department Pharmacovigilance / Drug Safety
    Position Associate Safety Data Management Specialist
    Location Chennai, India (Hybrid)
    Vacancies Not specified
    Required Education B.Pharm, M.Pharm, Pharm.D
    Experience Level Freshers Only
    Salary Range ₹4 LPA – ₹6 LPA (Estimated)
    Work Type Full-time (Hybrid)
    Application Link Pfizer Careers
  • Access Healthcare Hiring HCC Medical Coder roles

    Access Healthcare Hiring HCC Medical Coder roles

    HCC Medical Coder Vacancies – Certified Coders, 0.6–2 Yrs Exp – Chennai

    Apply for HCC Medical Coder roles at Access Healthcare, Chennai (Ambattur & Porur). Certified coders with 0.6–2 years’ experience eligible. Gingy and cory chase

    Access Healthcare, one of India’s leading healthcare business process outsourcing (BPO) and medical coding service providers, is inviting applications from certified HCC coders for their Chennai locations. With a strong focus on innovation, compliance, and career development, Access Healthcare provides an excellent platform for candidates looking to advance in the field of healthcare revenue cycle management.

    Company Overview

    Access Healthcare is a global provider of revenue cycle management, medical coding, billing, and healthcare outsourcing solutions. Known for its advanced technology platforms and world-class operations, the company empowers healthcare organizations to improve efficiency and compliance. With multiple delivery centers across India and abroad, Access Healthcare has become a trusted name for medical coding careers.

    Job Role & Responsibilities

    HCC Medical Coder / QA / QC

    • Perform Hierarchical Condition Category (HCC) coding in compliance with ICD-10-CM guidelines.
    • Ensure accuracy and completeness of clinical coding for risk adjustment.
    • Conduct QA/QC checks to maintain data integrity.
    • Collaborate with internal teams to achieve coding accuracy and productivity targets.
    • Work in a fast-paced environment with strict compliance and quality standards.

    Eligibility / Qualifications

    • Certification: AAPC or AHIMA-certified coders (CPC, COC, CRC, CCS, or equivalent).
    • Experience: 0.6 months to 2 years in HCC medical coding.
    • Shift: Day shift (Work from Office only).
    • Notice Period: 0 to 90 days accepted.

    Required Education & Courses: B.Sc Life Sciences, B.Pharm, M.Pharm, BDS, BHMS, BAMS, Nursing, or equivalent healthcare-related degrees.

    Location & Salary

    • Work Locations: Chennai – Ambattur Industrial Estate & Porur.
    • Compensation: Competitive salary package with industry-leading benefits.
    • Work Mode: Work from Office only.
    Apply for HCC Medical Coder roles at Access Healthcare
    Apply for HCC Medical Coder roles at Access Healthcare

    Application Process

    To apply, send your updated resume, recent photo, and Aadhar card to the HR contact below. Ensure to include the required details such as current company, experience, location, work preference (WFO only), certification number, salary details, and notice period.

    Contact for Interview Scheduling:
    Tharshini (HR) – +91 7550015097 (WhatsApp only – no calls)
    Email: tharshini.outsource@accesshealthcare.com

    FAQs

    1. Who can apply for HCC Medical Coder positions at Access Healthcare?
    Certified coders with CPC, COC, CRC, or equivalent from AAPC/AHIMA and 0.6–2 years’ coding experience.

    2. Is work-from-home (WFH) available for these roles?
    No, these are strictly Work from Office (WFO) positions in Chennai (Ambattur & Porur).

    3. What is the shift timing?
    Day shift only.

    4. What documents are required to apply?
    Updated resume, recent photo, Aadhar card, certification details, and salary details.

    5. How do I schedule an interview?
    Contact HR via WhatsApp (+91 7550015097) or email your details to tharshini.outsource@accesshealthcare.com.

    Quick Summary Table

    Company Access Healthcare
    Vacancies HCC Medical Coders (QA/QC roles also available)
    Required Education Life Sciences, B.Pharm, M.Pharm, BDS, BHMS, BAMS, Nursing, or equivalent
    Experience 0.6 months – 2 years in HCC coding
    Certification AAPC/AHIMA-certified (CPC, COC, CRC, CCS, etc.)
  • Associate STEM Content Analyst – MSc Chemistry Vacancy

    Associate STEM Content Analyst – MSc Chemistry Vacancy

    Apply now for Associate STEM Content Analyst role at Clarivate. Openings for M.Sc Chemistry graduates in Hyderabad & Chennai. Freshers eligible.

    Are you a chemistry graduate looking to kickstart your career in research, analysis, and intellectual property? Clarivate, a global leader in analytics and insights, is inviting applications for the Associate STEM Content Analyst role in Hyderabad and Chennai. This is an excellent opportunity for M.Sc Chemistry, General Chemistry, Organic Chemistry, or Pharmaceutical Chemistry graduates (0–1 year experience) who want to build expertise in chemical data analysis, intellectual property, and scientific research.

    Company Overview

    Clarivate is a trusted partner to the world’s most influential organizations, including pharmaceutical, chemical, medical services, and managed care companies. Each year, Clarivate supports clients in their strategic planning, technology management, competitive intelligence, and market development. Their dedicated chemistry team focuses on providing research-driven insights and market analysis that fuel the development of innovative drugs, chemical compositions, and research strategies.

    With more than 21+ members in the current team and continuous opportunities for professional growth, Clarivate is committed to fostering talent and building careers in STEM-driven industries.

    Job Role & Responsibilities

    As an Associate STEM Content Analyst, you will:

    • Analyze and interpret chemical processes from multiple data sources.
    • Draw and map chemical structures, adding specific codes to chemical structures.
    • Apply knowledge of chemical reactions, formulae, catalysts, and additives to generate insights.
    • Prepare detailed reports and communicate findings clearly and concisely.
    • Meet and exceed production volume and quality targets.
    • Record and monitor performance against targets.
    • Keep up-to-date with current developments in your domain area.
    • Maintain consistent quality standards across deliverables.
    • Demonstrate flexibility in adapting to process changes.
    • Assist team members as required and provide support in their absence.
    • Identify training and development needs and proactively upskill.
    • Follow safe working practices and adhere to compliance requirements.

    Eligibility / Qualifications

    Candidates applying for this role must meet the following criteria:

    • Educational Qualification: M.Sc in Chemistry, General Chemistry, Organic Chemistry, or Pharmaceutical Chemistry.
    • Experience: 0–1 year (freshers with relevant skills are encouraged to apply).
    • Technical Skills: Proficiency in chemical drawing tools such as ISIS Draw; familiarity with structure handling tools; strong knowledge of IUPAC nomenclature.
    • Core Skills:
      • Strong analytical and problem-solving ability.
      • Excellent attention to detail.
      • Clear and objective communication (written and spoken English).
      • Ability to interpret and analyze complex datasets.
      • Strong teamwork skills with the ability to work independently.

    Location & Salary

    • Work Locations: Hyderabad & Chennai (Hybrid model available).
    • Work Hours: Full-time, 40 hours per week, IST shift.
    • Salary: Competitive package based on qualifications and experience (discussed during the interview).
    Associate STEM Content Analyst – <a class=
    MSc Chemistry Vacancy” width=”1200″ height=”675″ /> Associate STEM Content Analyst – MSc Chemistry Vacancy

    Application Process

    Interested and eligible candidates can apply directly through Clarivate’s official careers portal:

    👉 Apply Now at Clarivate Careers

    We encourage candidates to apply early as applications may close soon.

    Why Join Clarivate?

    • Opportunity to work with global leaders in pharmaceutical, chemical, and healthcare research.
    • Hybrid work model offering flexibility and work-life balance.
    • Hands-on exposure to intellectual property, market research, and scientific insights.
    • Career progression and continuous learning through training opportunities.
    • Equal Employment Opportunity (EEO) workplace with diversity and inclusion at its core.

    FAQs

    Q1. Who can apply for the Clarivate Associate STEM Content Analyst role?
    M.Sc graduates in Chemistry, General Chemistry, Organic Chemistry, or Pharmaceutical Chemistry with 0–1 year experience can apply. Freshers are welcome.

    Q2. Do I need prior industry experience?
    No, freshers with relevant technical skills and academic knowledge are encouraged to apply.

    Q3. Is the role remote or on-site?
    The position is offered in Hyderabad and Chennai with a hybrid work model.

    Q4. What technical skills are preferred?
    Proficiency in chemical drawing tools (e.g., ISIS Draw), familiarity with structure handling tools, and strong knowledge of IUPAC nomenclature.

    Q5. What is the typical salary for Associate STEM Content Analyst at Clarivate?
    The salary is competitive and based on qualifications and experience, discussed during the interview.

    Call to Action

    If you are a passionate chemistry graduate eager to work in intellectual property and scientific research, don’t miss this opportunity.
    Apply today to secure your spot at Clarivate!

    👉 Submit Your Application Here

    Summary Table

    Company Clarivate
    Vacancies Multiple (Associate STEM Content Analyst)
    Required Education M.Sc Chemistry, General Chemistry, Organic Chemistry, Pharmaceutical Chemistry
    Experience 0–1 year (Freshers Eligible)
  • Freshers Certified Medical Coders | ASP RCM Solutions

    Freshers Certified Medical Coders | ASP RCM Solutions

    Freshers fayletha onlyfan leak Fayletha Certified Medical Coders | ASP-RCM Solutions Chennai

    ASP-RCM Solutions hiring fresh graduates for Certified Medical Coder (HCC Coding) role in Chennai. CPC/CRC certification preferred. Apply now!

    ASP-RCM Solutions is inviting fresh graduates to join its team as Certified Coders for HCC Coding at Kosmo One Tech Park, Ambattur, Chennai. This opportunity is ideal for candidates who want to start their careers in medical coding and healthcare revenue cycle management (RCM).

    Company Overview

    ASP-RCM Solutions is a trusted healthcare service provider specializing in revenue cycle management and medical coding. Driven by healthcare excellence and powered by experienced professionals, the company focuses on enabling providers with accurate coding, compliance, and optimized outcomes. Joining ASP-RCM means becoming part of a team committed to improving healthcare delivery and patient outcomes.

    Job Role & Responsibilities

    As a Certified Medical Coder – HCC Coding, freshers will be trained and guided to ensure accurate and compliant coding practices. Responsibilities include:

    • Applying medical coding knowledge to support accurate patient data recording.
    • Understanding and working with ICD-10-CM, CPT, and HCPCS coding systems.
    • Ensuring coding accuracy for regulatory compliance and optimized billing.
    • Working with healthcare providers to ensure coding supports patient care outcomes.
    • Using medical coding software and tools effectively.

    Eligibility / Qualifications

    • Education: Graduate from any recognized university.
    • Certification: CPC (Certified Professional Coder) and/or CRC (Certified Risk Adjustment Coder) preferred (AAPC or equivalent).
    • Experience: Freshers are eligible.

    Required Knowledge

    • Basic understanding of Anatomy, Physiology, and Medical Terminology.
    • Familiarity with ICD-10-CM, CPT, and HCPCS coding systems.

    Key Skills

    • Strong attention to detail and accuracy.
    • Good analytical and problem-solving skills.
    • Excellent oral and written communication.
    • Basic knowledge of medical coding software and computer systems.
    • Ability to adapt quickly and learn coding tools and guidelines.

    Location & Salary

    • Job Location: Kosmo One Tech Park, Ambattur, Chennai, Tamil Nadu.
    • Mode: On-site, full-time.
    • Salary: Competitive package offered (with additional benefits for certified coders).
    Freshers Certified Medical Coders | ASP-RCM Solutions
    Freshers Certified Medical Coders | ASP-RCM Solutions

    Application Process

    Interested candidates can apply by sending their updated resumes to: recruitment@asprcmsolutions.com

    For more details, candidates may also contact Joshua & Monisha at:
    📞 9240258189 / 9240258187
    📞 9384600158 / 9600707941

    Apply early to secure your opportunity with ASP-RCM Solutions and begin your career in healthcare coding!

    FAQs

    1. Who can apply for this role?
    Any graduate from a recognized university, preferably with CPC/CRC certification, can apply.

    2. Is this role open to freshers?
    Yes, this role is designed for freshers interested in medical coding.

    3. Is certification mandatory?
    CPC/CRC certification is preferred but not mandatory. ASP-RCM will train eligible candidates.

    4. What skills are most valued?
    Attention to detail, strong analytical abilities, communication skills, and knowledge of anatomy and medical terminology.

    5. What is the career growth potential?
    ASP-RCM Solutions provides training, certification support, and opportunities to grow in healthcare coding and RCM services.

    Career Benefits at ASP-RCM Solutions

    • Opportunity for freshers to enter the healthcare IT and medical coding industry.
    • Training and mentoring from experienced professionals.
    • Exposure to international healthcare coding standards.
    • Career advancement in medical coding, billing, and revenue cycle management.
    • Competitive pay packages with certification benefits.

    Summary Table

    Company ASP-RCM Solutions
    Vacancies Certified Coders for HCC Coding
    Required Education Graduate (any discipline)
    Experience Freshers
    Certification CPC/CRC preferred (AAPC or equivalent)
    Location Ambattur, Chennai, Tamil Nadu
  • Icon Plc Hiring Senior Pharmacovigilance Reporting Associate

    Icon Plc Hiring Senior Pharmacovigilance Reporting Associate

    Senior Pharmacovigilance Reporting Associate | ICON | Bangalore, Chennai, Trivandrum

    ICON plc hiring Senior Pharmacovigilance Reporting Associates in Bangalore, Chennai & Trivandrum. Apply now for drug safety careers with global benefits.

    ICON plc, a global leader in clinical research and healthcare intelligence, is inviting applications for the role of Senior Pharmacovigilance (PV) Reporting Associate across its Indian offices in Bangalore, Chennai, and Trivandrum. This role offers professionals a chance to contribute to patient safety worldwide while working in a diverse, inclusive, and innovation-driven environment.

    Company Overview

    ICON plc is recognized internationally as one of the top Contract Research Organizations (CROs), specializing in clinical development and data-driven healthcare solutions. With a mission to shape the future of clinical development, ICON partners with leading pharma and biotech companies to deliver cutting-edge drug safety, regulatory, and pharmacovigilance services. By joining ICON, professionals gain global exposure, advanced training, and access to robust employee benefits.

    Job Role & Responsibilities

    As a Senior Pharmacovigilance Reporting Associate, you will:

    • Prepare and submit adverse event (AE) reports and safety data in compliance with global regulatory requirements.
    • Collaborate with cross-functional teams including clinical and regulatory affairs to review and analyze safety data.
    • Contribute to Periodic Safety Update Reports (PSURs), Annual Reports, and DSURs.
    • Monitor reporting timelines, proactively resolving any delays.
    • Maintain pharmacovigilance databases with accuracy and integrity.
    • Provide training and mentorship to junior PV team members.
    • Support regulatory audits and inspections, ensuring compliance with pharmacovigilance guidelines.
    • Stay updated on evolving global safety regulations and industry standards.

    Eligibility / Qualifications

    • Education:
      • Bachelor’s degree in Life Sciences, Pharmacy, Biotechnology, or related fields (mandatory).
      • Advanced degree (Master’s/Ph.D.) preferred.
    • Experience:
      • Extensive prior experience in pharmacovigilance or drug safety reporting.
      • Proven knowledge of ICH-GCP, MedDRA, EudraVigilance, and FDA/EMA safety regulations.
    • Skills:
      • Strong analytical and data interpretation abilities.
      • Excellent written and verbal communication.
      • Proficiency in PV databases and Microsoft Office Suite.
      • Ability to manage multiple projects in fast-paced environments.
      • Commitment to confidentiality and regulatory compliance.

    Location & Salary

    • Locations: Bangalore, Chennai, Trivandrum (India)
    • Work Type: Office-based, full-time
    • Compensation: Competitive salary + country-specific benefits
    • Additional Benefits Include:
      • Health insurance options for employees and families
      • Life assurance
      • Retirement planning programs
      • Annual leave and flexible benefits (childcare vouchers, gym memberships, travel subsidies)
      • Employee Assistance Programme (EAP)
    Senior Pharmacovigilance Reporting Associate
    Senior Pharmacovigilance Reporting Associate

    Application Process

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

    Apply before the deadline to secure your spot in ICON’s global PV team and advance your career in drug safety.

    FAQs

    1. What is the main responsibility of this role?
    Ensuring timely and accurate reporting of safety data and adverse events in compliance with global regulations.

    2. What qualifications are required?
    A degree in Life Sciences, Pharmacy, or related fields, with advanced degrees preferred.

    3. How much experience is needed?
    Extensive experience in pharmacovigilance/drug safety reporting is required.

    4. What locations are hiring?
    ICON is hiring in Bangalore, Chennai, and Trivandrum.

    5. What benefits does ICON provide?
    Competitive salary, global health insurance, life assurance, retirement plans, flexible country-specific benefits, and professional growth opportunities.

    Quick Summary Table

    Company ICON plc
    Vacancy Senior Pharmacovigilance Reporting Associate
    Locations Bangalore, Chennai, Trivandrum
    Required Education Bachelor’s in Life Sciences/Pharmacy (Master’s preferred)
    Experience Extensive PV/Drug Safety Reporting experience
    Skills PV database expertise, regulatory compliance knowledge, communication skills
    Salary & Benefits Competitive pay, insurance, retirement, leave, global benefits
    Apply Link ICON Careers Portal