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Safety Submissions Specialist - Clinical Trial Services

Precision Medicine Group
2+ years
Not Disclosed
Bangalore, India
10 May 19, 2026
Job Description
Job Type: Full Time Hybrid Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title

Safety Submissions Specialist – Clinical Trial Services

Company

Precision Medicine Group

Division

Clinical Solutions

Location

Bangalore, Karnataka, India

Employment Type

Regular Full-time

Requisition Number

6488


Role Overview

The Safety Submissions Specialist is responsible for reviewing, preparing, and transmitting Individual Case Safety Reports (ICSRs) and other expedited safety reports to global regulatory authorities, business partners, affiliates, and other stakeholders.

The role requires expertise in global pharmacovigilance reporting regulations, safety databases, and regulatory submission processes, ensuring timely and compliant safety reporting for clinical trial programs.


Key Responsibilities

1. Safety Report Processing & Submission

  • Review and process Individual Case Safety Reports (ICSRs)

  • Prepare and submit expedited safety reports to:

    • Global regulatory agencies

    • Business partners

    • Affiliates

    • Other reporting destinations

  • Support both:

    • Paper submissions

    • Electronic submissions


2. Drug Safety Inbox & Acknowledgement Management

  • Monitor Drug Safety Inbox for:

    • Submission acknowledgements

    • Confirmation receipts

    • Incoming safety communications

  • Ensure timely follow-up and tracking of submissions


3. Regulatory Report Generation

  • Generate final clinical trial safety reports from the global safety database, including:

    • CIOMS I forms

    • MedWatch 3500A

    • XML reports

  • Prepare Investigator Safety Letters and final submission packages


4. Case Management & Documentation

  • Perform:

    • Case closure activities

    • Electronic filing of SAE documentation

    • Maintenance of safety records

  • Ensure all required documentation is properly archived and traceable


5. SAE Reconciliation & Compliance

  • Conduct:

    • SAE reconciliation activities

    • SUSAR Gap Pack reconciliation

  • Send queries and follow-up requests where required

  • Reconcile compliance metrics and submission tracking data


6. Deviation & CAPA Management

  • Manage expedited reporting deviations, including:

    • Deviation initiation

    • Investigation

    • Extension requests

    • CAPA (Corrective and Preventive Actions)

  • Support issue resolution and process compliance


7. Regulatory Intelligence & Reporting Plans

  • Monitor regulatory intelligence databases for:

    • Regulation updates

    • Country-specific reporting requirements

  • Support development and maintenance of Safety Reporting Plans


8. TMF & Compliance Management

  • Ensure submission of relevant documents to:

    • Trial Master File (TMF)

    • Pharmacovigilance System Master File (PSMF)

  • Maintain compliance with:

    • SOPs

    • Work Instructions (WIs)

    • GCP guidelines

    • ICH guidelines

    • GVP requirements

    • Global drug/device regulations


9. Operational Support

  • Maintain submission and distribution trackers

  • Update expedited email distribution lists

  • Attend departmental meetings and support ongoing operational activities


Required Qualifications

Education

  • BA/BS degree preferred


Required Experience

  • Minimum 2 years of experience in:

    • Clinical trial drug safety

    • Pharmacovigilance

    • Pharma or CRO industry

  • Experience with:

    • EMA EudraVigilance

    • UK MHRA

    • Other regulatory reporting portals


Required Technical Knowledge

  • Strong knowledge of:

    • FDA regulations

    • ICH guidelines

    • EU pharmacovigilance regulations

    • Global safety reporting requirements

  • Hands-on experience with:

    • ARGUS Safety Database

    • Electronic safety reporting systems


Required Skills & Competencies

Pharmacovigilance Skills

  • Understanding of:

    • SAE reporting

    • SUSAR processing

    • Safety submissions

    • Regulatory compliance

  • Knowledge of clinical trial safety operations


Operational Skills

  • Strong attention to detail and accuracy

  • Ability to manage multiple submission timelines

  • Strong organizational and tracking skills


Communication & Collaboration

  • Good written and verbal communication skills

  • Ability to work with cross-functional and global teams

  • Ability to support compliance and audit readiness activities


Work Environment

  • Office-based clinical safety environment

  • Collaboration with pharmacovigilance, regulatory, and clinical operations teams

  • Compliance-driven and deadline-oriented setting


Role Summary

The Safety Submissions Specialist is responsible for managing global safety submissions, expedited reporting, SAE reconciliation, and regulatory compliance activities for clinical trial programs. The role requires expertise in pharmacovigilance regulations, ARGUS safety systems, and global submission processes to ensure accurate and timely reporting to regulatory authorities and stakeholders.