FSP Medical Writing Program Manager (Remote; India)

Program Manager

At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development, and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on now and in the future.

We are excited to expand our Medical Writing FSP Team in India! We are seeking a Program Manager that has experience managing large-scale narrative projects. This role involves significant client engagement as well as opportunities to mentor and train medical writers.

Essential Functions :

• Develops, monitors, and adapts project plans, timelines, and budgets / forecasts for large programs.
• Serves as the point of contact for risk escalation, evaluating and resolving or escalating risks related to project quality, budget, or timeline.
• Ensures compliance with quality processes and requirements for assigned programs, maintaining consistency within and between project documents.
• Develops, reviews, and manages performance metrics for assigned projects.
• Provides senior-level review of project materials.
• Trains medical writers on processes and technical aspects of program management.
• May serve as primary author who writes and provides input on study- and program-level regulatory documents.

Education and Experience :

Bachelor's degree in a scientific discipline or equivalent and relevant formal academic / vocational qualification; Advanced degree preferred.

Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 8+ years).

Experience in managing and directing large medical writing narratives projects required.

Experience working in the pharmaceutical / CRO industry preferred.

Additional qualifications in medical writing (AMWA; EMWA; RAC) advantageous.

Knowledge, Skills, and Abilities :

What We Offer :

At PPD clinical research services we hire the best, develop ourselves and each other, and recognize the power of being one team. We understand that you will want to grow both professionally and personally throughout your career, and therefore at PPD clinical research services you will benefit from an award-winning learning and development programme, ensuring you reach your potential. As well as being rewarded a competitive salary, we have an extensive benefits package based around the health and well-being of our employees. We have a flexible working culture, where PPD clinical research services truly value a work-life balance. We have grown sustainably year on year but continue to offer a collaborative environment, with teams of colleagues eager to share expertise and have fun together. We are a global organization but with a local feel.

Our Mission is to enable our customers to make the world healthier, cleaner, and safer. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.