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Pv Coordinator - Fsp

Thermo Fisher Scientific
1+ years
₹4.5 LPA – ₹8 LPA
Hyderabad
15 Aug. 4, 2026
Job Description
Job Type: Full Time, Hybrid, Remote Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Labelling Assessment, MedDRA Coding, mRS and EQ-5D-5L, Triage of ICSRs, WHO DD Coding

PV Coordinator – Pharmacovigilance

Work Schedule: Standard (Monday–Friday)
Work Environment: Office-Based
Employment Type: Full-Time
Experience Required: 1+ Years

Salary Package

Expected CTC: ₹4.5 LPA – ₹8 LPA (Estimated market range based on pharmacovigilance case processing experience, Argus expertise, and organization. Actual compensation may vary.)

Job Summary

The PV Coordinator supports global pharmacovigilance programs by providing project coordination and safety operations support. The role involves managing serious and non-serious adverse event activities, protocol inquiries, safety documentation, Data Safety Monitoring Board (DSMB) and Endpoint Adjudication Committee (EAC) coordination, regulatory compliance support, and collaboration with Safety Specialists, Medical Monitors, clients, and internal teams.

The position requires strong organizational skills, attention to detail, and the ability to manage safety documentation and project deliverables within strict timelines.

Key Responsibilities

Pharmacovigilance Operations & Safety Coordination

  • Coordinate timely review of:

    • Serious Adverse Events (SAEs)

    • Non-Serious Adverse Events (NSAEs)

    • Protocol inquiries

    • Diagnostic safety information

    • Data Safety Monitoring Board (DSMB) data

  • Track safety information and generate reports for clients, project teams, and external vendors.

  • Perform safety documentation review and ensure accurate tracking of incoming safety information.

  • Support Safety Specialists and Medical Monitors in project execution activities.

  • Maintain accurate safety records and ensure audit readiness.

DSMB & Endpoint Adjudication Committee (EAC) Support

  • Represent the DSMB/EAC Coordination Team during global and domestic committee meetings.

  • Coordinate logistics for virtual and face-to-face committee meetings.

  • Collaborate with:

    • Clients

    • Board members

    • Third-party vendors

    • Internal project teams

  • Prepare meeting materials and support committee activities.

  • Compile adjudication dossiers and coordinate follow-up communication with investigative sites.

Project Coordination & Documentation Management

  • Support project implementation activities and maintain effective communication with stakeholders.

  • Prepare and manage contractual documents, including:

    • Confidentiality Disclosure Agreements (CDAs)

    • Letters of Intent (LOIs)

    • Member Agreements

  • Review documents for accuracy and coordinate internal and external approvals.

  • Coordinate project meetings, prepare meeting minutes, and distribute required materials.

  • Maintain project files, training records, and archival documentation.

  • Ensure pharmacovigilance activities remain inspection and audit ready.

Data Management & Compliance Activities

  • Perform safety data entry into internal and external databases and tracking systems.

  • Support reconciliation activities to identify data issues affecting project timelines.

  • Identify and redact subject identifiers according to privacy requirements.

  • Retrain sites on data privacy requirements and escalate repeated issues.

  • Maintain compliance with:

    • FDA regulations

    • ICH Good Clinical Practice (GCP)

    • Company SOPs

    • Client procedures and work practices

Administrative & Operational Support

  • Manage project expenses and coordinate translation activities within budget limits.

  • Respond to safety hotline calls and coordinate departmental activities.

  • Support local office activities as required.

  • Provide training and guidance to junior team members.

Required Qualifications

  • Graduation in Life Sciences or related healthcare discipline preferred.

  • Minimum 1 year of Pharmacovigilance case processing experience.

  • Experience working with Oracle Argus Safety Database is mandatory/preferred.

  • Understanding of adverse event processing and safety case management.

Required Skills

  • Knowledge of Pharmacovigilance processes and safety reporting requirements.

  • Experience handling adverse event cases and safety documentation.

  • Strong problem-solving and analytical skills.

  • Ability to work independently with minimal supervision.

  • Excellent communication and stakeholder management skills.

  • Ability to coordinate with clients, project teams, and external vendors.

  • Strong attention to detail and accuracy.

  • Ability to manage multiple tasks with strict deadlines.

  • Positive attitude with professional communication skills.

  • Ability to adapt to changing project priorities.

  • Strong computer skills, including:

    • Microsoft Word

    • Microsoft Excel

    • Microsoft PowerPoint

    • Microsoft Access

Preferred Skills

  • Experience supporting clinical trial safety operations.

  • Knowledge of DSMB and Endpoint Adjudication Committee processes.

  • Familiarity with FDA regulations, ICH-GCP guidelines, and pharmacovigilance SOPs.

  • Experience with safety databases and tracking systems.

  • Experience preparing safety reports and reconciliation activities.

  • Ability to train and mentor junior PV team members.

Working Conditions

  • Office-based role with standard Monday–Friday schedule.

  • Majority of work performed using computer-based systems.

  • Occasional travel to clinical sites may be required.

  • Occasional extended working hours based on project requirements.

  •