Oncology Scientific Lead, Med Com (Associate Scientific Dir)
Icon Clinical PLC · Boston, MA
FULL-TIME
Posted Jun 22, 2026
137,795–157,480 a year
Job Description
Experteer Overview
As Scientific Lead at ICON Global Medical Communications, you will oversee and approve scientific content, with increased independence on projects. You mentor junior writers and contribute therapy-area insights, while supporting account teams and internal initiatives. The role blends high-level writing, peer-review, and strategic client engagement in a hybrid capacity. You help manage project development from initiation to completion, including timelines and budgets, while advancing medical publications and communications. This is a values-driven role focused on quality, collaboration, and impact in patient-focused research.
Compensation / Benefits
• oversee and approve scientific/clinical content for assigned projects
• review writers’ outputs for accuracy and quality
• fact-check manuscripts and provide strategic insights related to therapy areas
• collaborate with Scientific Manager and account teams to meet timelines
• manage aspects of project development, including financials
• contribute to scientific/medical writing and content development as needed
• manage writers’ workloads and obtain background materials
• collaborate with graphics/editorial support to complete tasks
• mentor and onboard junior medical writers
• support business development through background research and writing for proposals
Tasks
• advanced degree (PhD preferred; MD/ PharmD considered)
• minimum 4–5 years in medical publications/medical communications with at least 3 years as Senior Medical Writer
• experience with high-level writing and review, ICMJE and GPP guidelines
• demonstrated mentoring ability and people management skills preferred
• strong client relationships and cross-functional collaboration experience
• familiarity with PubMed/Medline, clinicaltrials.gov, and data sources
• ability to work with cross-functional teams (editorial, graphics, presentations)
Key requirements
• competitive base salary and performance-related incentives
• health, dental, and vision coverage
• retirement and pension plans
• life assurance and disability coverage
• employee assistance programmes and wellbeing resources
• learning and development opportunities
As Scientific Lead at ICON Global Medical Communications, you will oversee and approve scientific content, with increased independence on projects. You mentor junior writers and contribute therapy-area insights, while supporting account teams and internal initiatives. The role blends high-level writing, peer-review, and strategic client engagement in a hybrid capacity. You help manage project development from initiation to completion, including timelines and budgets, while advancing medical publications and communications. This is a values-driven role focused on quality, collaboration, and impact in patient-focused research.
Compensation / Benefits
• oversee and approve scientific/clinical content for assigned projects
• review writers’ outputs for accuracy and quality
• fact-check manuscripts and provide strategic insights related to therapy areas
• collaborate with Scientific Manager and account teams to meet timelines
• manage aspects of project development, including financials
• contribute to scientific/medical writing and content development as needed
• manage writers’ workloads and obtain background materials
• collaborate with graphics/editorial support to complete tasks
• mentor and onboard junior medical writers
• support business development through background research and writing for proposals
Tasks
• advanced degree (PhD preferred; MD/ PharmD considered)
• minimum 4–5 years in medical publications/medical communications with at least 3 years as Senior Medical Writer
• experience with high-level writing and review, ICMJE and GPP guidelines
• demonstrated mentoring ability and people management skills preferred
• strong client relationships and cross-functional collaboration experience
• familiarity with PubMed/Medline, clinicaltrials.gov, and data sources
• ability to work with cross-functional teams (editorial, graphics, presentations)
Key requirements
• competitive base salary and performance-related incentives
• health, dental, and vision coverage
• retirement and pension plans
• life assurance and disability coverage
• employee assistance programmes and wellbeing resources
• learning and development opportunities
Benefits
- Health insurance
- Dental insurance
Additional Details
- City
- Boston
- State
- Massachusetts
- Country
- US
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