- Location
- Waltham, MA
- Workplace
- Onsite
- Type
- Full-time
- Department
- Openings
- Seniority
- Entry
- Experience
- 2+ years
- Source
- Lever
Description
Crescent Biopharma’s vision is to build a world leading oncology company bringing the next wave of therapies for cancer patients. The Company’s clinical-stage pipeline includes its lead program, a PD-1 x VEGF bispecific antibody, as well as novel antibody-drug conjugates. By leveraging multiple modalities and established targets, Crescent aims to rapidly advance potentially transformative therapies as single agents and as part of combination regimens to treat a range of solid tumors. For more information, visit www.crescentbiopharma.com and follow the Company on LinkedIn and X.
We are seeking a Clinical Trial Associate (CTA) will work with the Clinical Study Lead and Director of Clinical Operations to support the conduct of clinical trials. The CTA will partner with the Clinical Study Lead to ensure studies are completed on time, within budget, and in compliance with SOPs, FDA regulations and ICH/GCP guidelines.
CTA may independently manage components of clinical studies, including but not limited to vendor oversight, budgets, responsibility for a subset of sites or countries, or phases of the trial (startup period, for example), with oversight.
Skills
GCPExcelClinical TrialsFDACompliance
Benefits
Opportunity to join a mission-driven team where you'll contribute to impactful work, take on varied responsibilities, and grow quickly in a dynamic environmentCompetitive compensation, including base salary, performance bonus, and equity100% employer-paid benefits packageFlexible PTO; also, two, one-week company-wide shutdowns each yearA commitment to your professional development, with access to resources, mentorship, and growth opportunities
