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Icf Medical Writing Program Manager

8+ years
Not Disclosed
10 Nov. 25, 2025
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, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

ICF Medical Writing Program Manager – Remote (India)

Category: Clinical Research
Job Type: Full-Time
Location: Fully Remote, India


About the Opportunity

Join a leading global Contract Research Organization (CRO) supporting the PPD® clinical research portfolio. Our team plays a critical role in accelerating clinical development and ensuring patient-centric medical writing excellence across global programs. As an ICF Medical Writing Program Manager, you will lead end-to-end development of Informed Consent Forms (ICFs) while managing high-visibility client relationships, program timelines, quality standards and operational efficiency.

This role is ideal for experienced clinical or medical writing professionals who excel in program management and client-facing leadership.


Key Responsibilities

  • Lead end-to-end management of complex ICF medical writing programs for global clients.

  • Develop, monitor, and refine project plans, timelines, standards, budgets, and forecasts.

  • Serve as primary liaison across cross-functional teams to ensure quality deliverables and resource alignment.

  • Oversee project progress using tracking tools and ensure timely completion of all contracted deliverables.

  • Identify project risks related to quality, timelines, or budget and escalate or resolve appropriately.

  • Ensure compliance with organizational quality standards and regulatory guidelines.

  • Support business development by preparing proposal content, budgets, presentations, and participating in client meetings.

  • Mentor and train junior program managers in ICF processes and program management best practices.

  • Contribute to continuous improvement of departmental processes, metrics, and performance standards.


Education and Experience Requirements

  • Bachelor’s degree in a scientific discipline; advanced degree preferred.

  • Minimum 8+ years of relevant experience with a bachelor’s degree OR 6+ years with an advanced degree.

  • Proven experience managing medical writing or clinical research projects.

  • Strong background in pharmaceutical or CRO industry operations.

  • Experience in medical writing (regulatory or plain-language writing) preferred.

  • Demonstrated ability to manage client relationships and complex multi-document programs.


Key Skills and Competencies

  • Advanced project management skills including forecasting, budgeting, and resource planning.

  • Strong organizational skills with the ability to effectively prioritize multiple deadlines.

  • Excellent written and verbal communication skills for cross-functional and client interactions.

  • Strong negotiation, problem-solving, and decision-making abilities.

  • Deep knowledge of global regulatory and document development guidelines relevant to patient-centric deliverables.

  • High degree of independence and sound judgment in managing technical and operational challenges.

  • Ability to lead and mentor junior team members effectively.


Work Schedule

  • Second Shift (Afternoon shift)

Work Environment

  • Remote work setting with adherence to organizational quality and documentation standards.


This position offers a unique opportunity to lead impactful patient-centric writing programs that support global clinical development. Candidates with strong leadership capabilities, proven project management skills, and significant medical writing experience are encouraged to apply.