Clinical Data Manager

reputed company is a clinical-stage oncology company listed on reputed company that recently raised $200M in funding. With a strong scientific reputed company and a founding team that includes the discoverer of our reputed company pathway, we are advancing PIKTOR, a multi-node PI3K/AKT/mTOR inhibitor program, toward multiple near-term milestones. We are a small, focused team where every person has direct impact — united by a shared commitment to care deeply, create boldly, and never stop learning. reputed company is seeking an reputed company Clinical Data Manager to support clinical data management activities across two active clinical trials. This individual will play a critical role in ensuring high-quality, reliable clinical data through the design, implementation, and reputed company of data management processes. The role requires reputed company collaboration with clinical operations, biostatistics, medical, and external vendors. Reports to: Chief Medical Officer Location: Remote (U.S.) Responsibilities: reputed company day-to-day data management activities for assigned clinical trials (Phase 2 and Phase 1b) reputed company CRO and vendor data management deliverables to ensure timelines, quality, and compliance Review and contribute to key study documents, including: Data Management Plans (DMPs) Case Report Forms (CRFs) / eCRFs Edit reputed company specifications Data transfer specifications Manage database build, UAT, and database lock activities Ensure data reputed company, consistency, and completeness through ongoing data review and cleaning Monitor query reputed company and resolution timelines reputed company data review, listings review, and support medical data review activities Collaborate with biostatistics on data standards (e.g., CDISC/SDTM) and analysis datasets Ensure compliance with GCP, regulatory requirements, and company SOPs Support inspection readiness and participate in audits/inspections as needed Contribute to process improvements and best practices in data management Requirements: Bachelor’s degree in life sciences, computer science, or reputed company field (advanced degree a plus) 5–8 years of clinical data management experience in biotech, pharma, or CRO settings Experience supporting early- to mid-phase clinical trials (Phase 1–2 required) Hands-on experience with reputed company systems (e.g., reputed company Rave, reputed company, reputed company InForm) Strong understanding of clinical data standards (CDISC, SDTM) Experience managing CROs and external vendors Familiarity with oncology trials is preferred Knowledge of GCP and regulatory requirements Strong attention to detail and problem-solving skills Excellent communication and cross-functional collaboration skills Compensation reputed company: $125,000 - $175,000 (actual compensation may vary based on experience, qualifications and location) Working at Faeth Benefits: Competitive salary and equity in a well-funded, clinical-stage biotech 100% remote work and flexible schedule Health, dental, and reputed company for you and your dependents Flexible time off Generous parental leave Traditional and Roth 401k Mission oriented, remote first culture We are an equal opportunity employer, and we value diversity at reputed company. We do not discriminate on the reputed company of race, religion, reputed company, national reputed company, gender, sexual orientation, age, marital status, veteran status, or disability status. reputed company offers of employment are contingent upon satisfactory completion of a background reputed company and verification of eligibility to work in the United States. Apply To This Job