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Senior Dmc Project Coordinator

2-6 years
Not Disclosed
10 Nov. 11, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior DMC Project Coordinator – Structured Job Description

Location: Bangalore
Category: Clinical
Job ID: 255456


🔹 Summary of Responsibilities

1. DMC Coordination & Support

  • Coordinate and manage all activities related to Data Monitoring Committees (DMCs).

  • Tasks include:

    • Timeline creation

    • Selection and contracting of DMC members

    • Review of DMC contracts

    • Development of DMC Charters

    • Organizing travel, meetings, and logistics

    • Preparing meeting materials, attending meetings, preparing minutes

    • Managing expense reporting

2. Project & Workflow Management

  • Track project workflows to ensure all DMC deliverables meet required deadlines.

  • Ensure project activities stay within the assigned budget.

  • Identify out-of-scope tasks and escalate issues appropriately.

  • Create and maintain DMC tracking tools and progress reports.

3. Stakeholder Communication

  • Act as the primary liaison between:

    • Sponsor

    • DMC members

    • Internal project teams

  • Lead internal DMC support meetings and document outcomes.

  • Provide guidance to clients and internal teams on DMC processes.

4. Quality Oversight & Documentation

  • Perform quality control on specified DMC deliverables.

  • Maintain and update project-specific documents including:

    • Study Master Files

    • Archival and storage documentation

  • Ensure high-quality deliverables through ongoing QC and corrective actions.

5. Mentorship & Team Collaboration

  • Mentor and support junior DMC Project Coordinators.

  • Maintain high professional standards while collaborating across Clinical Development Services.

6. Compliance

  • Follow Fortrea SOPs, GCP guidelines, and quality systems.

  • Ensure all activities meet regulatory and internal compliance standards.


Minimum Qualifications

  • Bachelor’s degree or higher in a health-related field.

  • Relevant experience may be considered in place of formal education.


Required Experience (2–6 Years)

Must include:

  • Direct experience with Data Monitoring Committees (DMCs).

  • Additional relevant experience in:

    • Clinical

    • Safety

    • Data Management

    • Pharmaceutical/CRO industry

Core Skills

  • Strong attention to detail

  • Excellent teamwork

  • Ability to work independently with minimal guidance

  • Capable of managing multiple priorities

  • Strong problem-solving and decision-making skills

  • Good customer focus

  • Strong verbal and written communication

  • Good working knowledge of clinical trial processes

  • Proficiency in Word, Excel, PowerPoint

  • Strong project management and organizational skills

  • Ability to meet strict timelines with high-quality output

  • Professional, discreet communication style


Work Environment

  • Office-based or home-based (depending on line manager’s direction).