FREE ACCESS
5,000–10,000 jobs/day

See all jobs on JobTailor
Search thousands of fresh jobs every day.
Discover
- Fresh listings
- Fast filters
- No subscription required
Create a free account and start exploring right away.

Senior Clinical Trial Manager – Global
Bicara TherapeuticsSenior Clinical Trial Manager overseeing operational execution of global clinical trials at Bicara Therapeutics. Partnering with cross-functional teams in a hybrid role based in Boston.
Posted 6/18/2026full-timeBoston • Massachusetts • 🇺🇸 United StatesSenior💰 $179,000 - $211,000 per yearWebsite
About the role
Key responsibilities & impact- Execute Bicara’s clinical operations strategy of high-touch, patient-centered clinical trials with a strong focus on adaptive and seamless designs to support registration.
- Support clinical operations team in ensuring all trial deliverables are met according to timelines, budget, operational procedures, and quality standards.
- Work closely with external collaboration partners with a focus on relationship management and efficiency.
- Lead the proactive identification, assessment, and management of clinical study challenges and risks.
- Support the oversight of all study activities including site identification and selection, enrollment models, clinical supply planning, budget planning and trial execution.
- Monitor oversight of study progress including: CRO and third-party vendors, ensuring compliance with relevant regulations and guidelines by maintaining regular contact with external vendors, including CRAs, as applicable.
- Work with CRO to develop and/or revise scope of service agreements, budgets, plans and detailed timelines and ensure that performance expectations are met.
- Participate in the development and authorship of study documents including protocol, investigator brochure, informed consent, etc.
- Participate in Case Report Form design and user acceptance testing in partnership with Data Management as well as data monitoring over the course of the study.
- Oversee study management and/or clinical development teams (CROs) to facilitate clinical development goals and achievement of study quality metrics.
- Execute CRO/Third Party Oversight Activities including but not limited to: Monitoring visit report review, periodic review of data quality, review of CRO/Vendor KPIs, performing Sponsor Oversight Visits, etc.
- Contribute to and/or author clinical sections of regulatory documents including Investigators’ Brochures, safety updates, and responses to Health Authority / Ethics Committee questions.
Requirements
What you’ll need- Bachelor's Degree is required, preferably in Life Sciences (e.g., Biology, Chemistry, Biochemistry, Nursing, Pharmacy).
- Minimum of 5 years’ clinical trial management experience in the pharmaceutical, biotech and/or CRO industry.
- Demonstrated ability to manage global clinical trials, navigating regional regulatory requirements, cultural nuances, and varying site capabilities across multiple geographies.
- Phase 2/Phase 3 study experience strongly preferred.
- Oncology study experience strongly preferred.
- Clinical research operational knowledge, computer literacy, and strong project planning/management including oversight of CROs/vendors.
- Global clinical trial management in fast paced CRO outsourced environment required.
- Experience and ability to manage global or regional teams in a virtual environment.
- Strong decision-making and communication/collaboration skills are essential to this position, as are analytic skills and effectiveness in seeking solutions to issues.
- Must be adaptable and enjoy working in a fast-paced environment.
- Effective leadership skills and proven ability to foster team productivity, cohesiveness, and quality deliverables.
- Willingness to travel up to 10-20% of the time.
Benefits
Comp & perks- medical, dental, and vision coverage upon hire
- short term and long term incentives including cash bonus and equity incentive opportunities
- comprehensive benefits and wellness package
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial managementadaptive designsseamless designsbudget planningdata monitoringCase Report Form designregulatory document authorshipproject planningclinical research operational knowledgeCRO oversight
Soft Skills
relationship managementdecision-makingcommunicationcollaborationanalytical skillsadaptabilityleadershipteam productivityproblem-solvingcultural awareness
Certifications
Bachelor's Degree in Life Sciences