Clinical Science Lead, Study Design & Strategy

Relay Therapeutics; Cambridge (MA); On-site; USD 150,000 - 210,000; Full time

Job summary

Relay Therapeutics in Cambridge, MA is seeking a Manager, Clinical Science to drive asset development and implement the clinical strategy. You will collaborate with clinical PM, regulatory affairs, operations, biostatistics, data management and medical writing to advance studies and provide strategic scientific input.

You will design studies, direct protocol development, oversee DSUR timelines, and support regulatory questions while ensuring data quality and integrity across initiatives with

Qualifications

• Advanced degree in life sciences with 2+ years in pharma/biotech.
• Deep understanding of clinical development phases and study design.
• Strong knowledge of ICH and GCP regulations.

Responsibilities

• Contribute to the design of clinical studies with Medical Lead and Development teams.
• Lead or contribute to protocol development and translation into executable trials.
• Drive medical input for IB, DSUR updates with cross-functional teams.
• Support regulatory queries and submissions related to studies.
• Perform medical data review and analysis; assess protocol deviations.
• Assist in eCRF design and data capture per protocol.
• Support data cleaning and analyses for regulatory submissions and publications.
• Monitor real-time study data with Clinical Operations to resolve issues.
• Review literature for competitive intelligence and contribute to publications.
• Foster collaboration with stakeholders, including investigators and experts.

Skills

Clinical study design

Cross-functional collaboration

Regulatory submissions

Data interpretation

Strategic scientific input

Education

PhD or MS in life sciences

PharmD

BSN

Job description

Relay Therapeutics in Cambridge, MA is seeking a Manager, Clinical Science to drive asset development and implement the clinical strategy. You will collaborate with clinical PM, regulatory affairs, operations, biostatistics, data management and medical writing to advance studies and provide strategic scientific input.

You will design studies, direct protocol development, oversee DSUR timelines, and support regulatory questions while ensuring data quality and integrity across initiatives with