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Senior Dmc Project Coordinator

2-6 years
Not Disclosed
10 Nov. 13, 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

Position Title: Senior DMC Project Coordinator

📍 Location: Bangalore, India
🏢 Department: Clinical
🆔 Job ID: 255456
💼 Employment Type: Full-Time


Job Summary

The Senior Data Monitoring Committee (DMC) Project Coordinator is responsible for managing and supporting all operational activities associated with Data Monitoring Committees. This includes coordination of DMC logistics, documentation, communication between sponsors and committees, and ensuring compliance with timelines, budgets, and quality standards.


Key Responsibilities

1. DMC Coordination & Operations

  • Coordinate and support all activities for Data Monitoring Committees (DMCs), including:

    • Timeline generation and progress tracking

    • Selection and contracting of DMC members

    • Development and review of DMC charters

    • Organizing travel and logistics

    • Preparing, attending, and documenting DMC meetings

    • Managing expense reports and follow-up actions

  • Monitor workflow and project status to ensure that all DMC deliverables and deadlines are met.

  • Ensure all project activities are conducted per Fortrea SOPs, Quality Management System (QMS), and Good Clinical Practice (GCP) guidelines.


2. Project Management & Compliance

  • Maintain compliance with project budgets, identifying and escalating potential out-of-scope work or issues to management.

  • Develop and manage DMC tracking tools, reports, and dashboards for effective project oversight.

  • Conduct and document internal DMC support team meetings and ensure timely follow-ups.

  • Maintain all project-specific documentation, including setup and maintenance of Study Master Files (SMFs).

  • Perform quality control (QC) checks on DMC deliverables to ensure accuracy and completeness.


3. Client & Team Communication

  • Act as a primary liaison between the sponsor, DMC members, and internal Fortrea project teams.

  • Provide guidance and support to clients and internal teams regarding DMC processes and expectations.

  • Present and communicate project updates effectively across functions.

  • Build and maintain strong professional relationships within Clinical Development Services and with external stakeholders.


4. Leadership & Mentoring

  • Provide mentoring, oversight, and quality review for less experienced DMC Project Coordinators.

  • Contribute to training initiatives and help standardize DMC processes across teams.

  • Promote high-quality work standards through ongoing review and process improvement.


Qualifications

Education

  • Bachelor’s degree or higher in a health-related field (e.g., Pharmacy, Life Sciences, Nursing, Biotechnology).

  • Equivalent or relevant experience may be considered in lieu of formal education.


Experience Requirements

Category

Requirement

Experience Range

2–6 years total experience

Core Experience

Direct experience coordinating or managing DMCs (Data Monitoring Committees)

Relevant Experience

At least 2 years in Clinical Research, Safety, or Data Management within pharmaceutical, biotechnology, or CRO settings

Technical Skills

Proficiency in Microsoft Word, Excel, and PowerPoint

Knowledge Areas

Understanding of the clinical trial process, GCP, project management principles


Core Competencies

  • Exceptional attention to detail and organizational skills

  • Strong team player with the ability to work independently under limited supervision

  • Excellent verbal and written communication skills

  • Capable of managing multiple concurrent priorities effectively

  • Problem-solving mindset with proactive issue identification and resolution

  • Customer-focused and able to maintain professionalism at all times

  • Ability to adhere to strict timelines and maintain high-quality standards

  • Demonstrated project management and coordination capabilities


Work Environment

  • Work Mode: Office-based or home-based (as per line manager’s discretion)

  • Work Culture: Collaborative, professional, and quality-driven

  • Physical Demands: Standard office requirements


Equal Opportunity Statement

Fortrea is an Equal Opportunity Employer committed to diversity and inclusion in all aspects of employment. Reasonable accommodations will be provided upon request for qualified individuals with disabilities.

Learn more about EEO & Accommodation policies here.