Clinical Science Lead, Phase 3 Trial (Onsite)

Kailera Therapeutics; Boston (MA); On-site; USD 159,000 - 195,000; Full time

Benefits offered by this job

Health coverage

Wellness stipend

401(k) match

Tuition reimbursement

Commuter benefits

Equity grants

Job summary

Kailera Therapeutics seeks an Associate Director, Clinical Scientist to lead and execute Phase 3 clinical trials, working closely with Medical Directors and cross-functional teams. This on-site role in Waltham, MA involves end-to-end trial oversight, data review, and strategic input to study design and reporting.

The ideal candidate brings 5+ years in clinical development, strong leadership and communication skills, and a deep understanding of the drug development life cycle across preclinical

Qualifications

• 5+ years experience in clinical development and trials.
• Experience leading cross-functional study teams.
• Experience reviewing clinical trial data listings.
• Strong understanding of drug development process.

Responsibilities

• Support Medical Directors for Phase I–III studies.
• Lead studies across full trial lifecycle from start-up to database lock.
• Provide scientific input on efficacy and safety endpoints.
• Identify data trends and issues with Data Management and Biostatistics.
• Collaborate with Clinical Operations, Data Management, Biostatistics, Programming, Safety and Regulatory.
• Provide clinical oversight of study execution and ensure alignment with strategy.
• Author/review trial documents including protocols and CRFs.
• Develop and deliver presentations to study teams.

Skills

Clinical trial leadership

Cross-functional collaboration

Data interpretation

Study start-up

Scientific communication

Project management

Education

RN, MS, PhD or PharmD

Tools

SAS

EDC systems

Job description

Kailera Therapeutics seeks an Associate Director, Clinical Scientist to lead and execute Phase 3 clinical trials, working closely with Medical Directors and cross-functional teams. This on-site role in Waltham, MA involves end-to-end trial oversight, data review, and strategic input to study design and reporting.

The ideal candidate brings 5+ years in clinical development, strong leadership and communication skills, and a deep understanding of the drug development life cycle across preclinical