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Lifelancer$245K – $260K per yearUnited States only
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First Shift (Days) Environmental Conditions
Join Us as the FSP Functional Lead for Medical Writing!
At Thermo Fisher Scientific, you’ll 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.
The FSP Functional Lead for Medical Writing is responsible for the Medical Writing FSP portfolio, providing global strategic direction, creative solutions, medical writing expertise and oversight to internal and external clients.
This role involves developing the departmental organizational structure, as well as recruiting, training, and motivating staff to ensure performance excellence.
The FSP Functional Lead for Medical Writing also leads the implementation of changes in departmental remit, processes, and operations to align Medical Writing regionally with the strategic direction and goals of the organization.
Provides program-level and strategic oversight to one or more Medical Writing groups, developing and communicating the strategic direction for the groups.
Recruits, engages, manages, and motivates staff to ensure excellence in performance.
Develops an organizational structure and communicates departmental goals and priorities.
Leads the implementation of changes in departmental remit, processes, and operations to developthe group in line with the strategic direction and goals of the organization.
Develops and leads development and management of the departmental budget.
Promotes and advocates for the business needs of the Medical Writing group.
Builds relationships with other PPD departments and seeks opportunities to collaborate with other functions for mutual benefit (e.g., Phase I medical writing, Pharmacokinetic, biostatistics, pharmacovigilance, regulatory).
Leads collaborative working relationships with business development and senior management insecuring new business by making presentations to clients, conducting contract negotiations,developing, and reviewing proposal texts and budgets, in collaboration with Proposal & ContractsDevelopment.
Resolves or escalates serious project issues and risks to senior management. Prepares reportsregarding significant project issues to senior management as needed.
Provides accountability and leadership in handling complex client management issues.
Assumes primary responsibility for the visibility and reputation of the Medical Writing group withinPPD.
Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 15+ years) or equivalent and relevant combination of education, training, & experience.
Excellent project management skills, including the ability to organize, plan and manage projects, create and modify budgets, develop timelines, allocate resources, and forecast departmental workload
Excellent knowledge of global/regional medical writing/regulatory requirements for clinical trials, marketing authorization and late phase procedures; experience across the product development lifecycle
Demonstrated ability to build teams, maintain collaborative relationships, initiate cross-functional mentoring; anticipate resistance; influence without authority and provide a senior-level presence when necessary
When you join Thermo Fisher Scientific, you become part of a global team that values passion, innovation, and a commitment to scientific excellence. You’ll work in an environment where collaboration and development are part of the everyday experience—and where your contributions truly make a difference.
Apply today to help us deliver tomorrow’s breakthroughs.
The salary pay range estimated for this position Director Medical Writing based in Maryland is $245,000.00–$260,000.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy. We offer a comprehensive Total Rewards package that our U.S. colleagues and their families can count on, which includes:
At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy
Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount
This job is curated by Lifelancer .
Lifelancer is a talent-hiring platform in Life Sciences, Pharma and IT. The platform connects talent with opportunities in pharma, biotech, health sciences, healthtech and IT domains.
Opens the original posting on Himalayas.
Apply nowSource: Himalayas