The Associate Director serves as a key strategic partner to senior clinical leadership for determining medical writing strategies across therapeutic areas
Job Summary
The Associate Director serves as a key strategic partner to senior clinical leadership for determining medical writing strategies across therapeutic areas.
This role is accountable for leading cross-functional teams to develop messaging strategies that ensure regulatory submissions are compelling, accurate, and consistent.
The position requires managing a team of Senior Medical Writers while overseeing budgeting, resource planning, and the efficient preparation of high-quality deliverables.
Matching Summary
The Associate Director serves as a key strategic partner to senior clinical leadership for determining medical writing strategies across therapeutic areas.
Skills & Requirements
Must-have
8 years medical writing experience
3 years supervisory role
CTD format submission experience
Cross-functional team leadership
Clinical development strategy
Nice-to-have
PhD or MD preferred qualification
Global therapeutic area expertise
Vendor governance participation
eCTD and EDMS knowledge
Lifecycle management work
Key Requirements
Minimum 8 years medical writing experience in biopharma or CRO
Minimum 3 years in a supervisory role
Post-graduate qualifications (PhD or MD preferred)
Mastery of English language grammar and punctuation
Prior experience with Common Technical Document (CTD) submissions