FSP Medical Writing Program Manager – Remote (India)
Job ID: R-01331944
Location: Remote, India
Employment Type: Full-Time
Category: Clinical Research / Medical Writing
Work Mode: Fully Remote
Work Schedule: Monday to Friday
About the Company
Thermo Fisher Scientific, through its PPD® Clinical Research Services portfolio, is a global leader in contract research, supporting the development and delivery of life-changing therapies. With clinical trials conducted in over 100 countries, the organization delivers integrated laboratory, digital, and decentralized clinical trial solutions. Thermo Fisher Scientific’s mission is to enable customers to make the world healthier, cleaner, and safer.
Job Overview
Thermo Fisher Scientific is expanding its Medical Writing Functional Service Provider (FSP) team in India and is seeking an experienced Medical Writing Program Manager. This leadership role is ideal for professionals with strong experience managing large-scale medical writing and narrative development programs within the pharmaceutical or CRO environment.
The position involves strategic program oversight, direct client interaction, quality and risk management, and mentoring of medical writing teams across global projects.
Key Responsibilities
Develop, manage, and continuously optimize project plans, timelines, and budgets for large medical writing programs
Act as the primary point of contact for risk identification, escalation, and resolution related to quality, timelines, or financial performance
Ensure compliance with internal quality standards and global regulatory document development guidelines
Maintain consistency and accuracy across study-level and program-level documentation
Define, track, and report performance metrics for assigned projects
Provide senior-level scientific and editorial review of medical writing deliverables
Train and mentor medical writers on program management processes and technical requirements
Contribute as a primary author or reviewer for study-level and program-level regulatory documents when required
Effectively lead cross-functional study teams and collaborate with global stakeholders
Required Education and Experience
Bachelor’s degree in a scientific discipline (Life Sciences, Pharmacy, Medicine, or related field); advanced degree preferred
Minimum 8+ years of relevant experience in medical writing, clinical research, or regulatory documentation
Proven experience managing large-scale medical writing or narrative development programs
Prior experience within a pharmaceutical company or CRO environment preferred
Professional certifications such as AMWA, EMWA, or RAC are advantageous
Required Skills and Competencies
Strong project and program management capabilities, including resource planning and multi-writer coordination
Excellent medical writing, data interpretation, editorial, and proofreading skills
In-depth knowledge of global and regional clinical and regulatory document development standards
Exceptional written and verbal communication and presentation skills
Strong leadership, negotiation, and stakeholder management abilities
High level of independence, sound judgment, and problem-solving skills
Ability to mentor, coach, and develop junior and mid-level medical writers
Adaptability in a fast-paced, global clinical research environment
What the Company Offers
Competitive compensation aligned with global standards
Comprehensive benefits package focused on employee health and well-being
Flexible and fully remote working model supporting work-life balance
Access to award-winning learning and development programs
Collaborative, inclusive, and growth-oriented work culture
Opportunity to work on global clinical research programs with meaningful impact
Company Values
Thermo Fisher Scientific operates with a strong commitment to Integrity, Intensity, Innovation, and Involvement. With a global workforce of over 100,000 professionals, the organization values diversity, collaboration, and scientific excellence.
Apply Now
Advance your career in global clinical research and medical writing leadership. Join PPD, part of Thermo Fisher Scientific, and contribute to accelerating research that improves lives worldwide.
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