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Senior/Lead Medical Reviewer

Navitas Lifesciences
Navitas lifesciences
1-3 years
Not Disclosed
Bangalore, India
10 April 21, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing

Job Title: Senior / Lead Medical Reviewer

Department: Pharmacovigilance / Drug Safety

Experience Required: 1–3+ Years (Aggregate Reporting, Signal Management, or RMP)


Role Overview

The Senior / Lead Medical Reviewer is responsible for reviewing and managing aggregate safety reports, ensuring medical accuracy, regulatory compliance, and timely delivery. The role includes team mentoring, stakeholder coordination, and oversight of pharmacovigilance activities.


Key Responsibilities

1. Safety Writing & Medical Review

  • Review and ensure medical consistency of aggregate reports such as:

    • Risk Management Plans (RMPs)

    • Periodic Safety Update Reports (PSURs)

    • PBRERs, DSURs, PADERs, and Canadian Aggregate Reports

  • Author and review safety documents as required

  • Ensure high-quality, accurate, and compliant safety reporting

2. Project & Operational Management

  • Oversee service performance and ensure timely delivery within budget and quality standards

  • Manage logistical aspects of report development and submission

  • Coordinate with cross-functional authors to meet client and regulatory expectations

  • Assist in scheduling, allocation, and tracking of reports

3. Team Leadership & Mentoring

  • Mentor and guide team members to work independently and efficiently

  • Conduct training sessions to improve team performance

  • Ensure completion of required organizational and client-specific training

  • Lead daily status meetings and support team productivity

4. Compliance & Quality Assurance

  • Ensure compliance with internal SOPs, work instructions (WIs), and client procedures

  • Support development and updating of SOPs and guidance documents

  • Maintain and update project trackers and documentation

  • Ensure adherence to pharmacovigilance and regulatory requirements

5. Stakeholder & Client Management

  • Act as the point of contact for aggregate reporting teams and clients

  • Develop and present project-specific slides for internal and external stakeholders

  • Provide expert input for report finalization and issue resolution

6. Audit & Inspection Support

  • Participate in internal and external audits and regulatory inspections

  • Ensure audit readiness and compliance with health authority requirements

7. Cross-Functional Support

  • Assist Individual Case Safety Report (ICSR) teams as needed

  • Support literature review teams based on workload

  • Collaborate with multiple departments for seamless project execution


Required Skills & Competencies

  • Strong understanding of pharmacovigilance and medical terminology

  • Knowledge of aggregate safety reporting processes and documentation

  • Excellent writing, review, and analytical skills

  • Strong organizational and multitasking abilities

  • Effective communication and stakeholder management skills


Technical Skills

  • Proficiency in Microsoft Office (Word, Excel, PowerPoint)

  • Familiarity with pharmacovigilance databases and reporting tools (preferred)


Regulatory Knowledge

  • Good understanding of:

    • GCP, GVP, and ICH guidelines

    • USFDA and global pharmacovigilance regulations

  • Awareness of patient safety and regulatory reporting obligations


Preferred Experience

  • Experience in aggregate reporting, signal management, or RMP

  • Exposure to regulatory submissions and pharmacovigilance processes

  • Familiarity with global safety reporting standards


Personal Attributes

  • Strong leadership and mentoring skills

  • High attention to detail and accuracy

  • Ability to work under deadlines and manage multiple priorities

  • Team-oriented with strong interpersonal skills

  • Reliable, structured, and proactive approach to work