Faeth Therapeutics · 3 months ago
Senior Clinical Scientist
United States
Full-time
Remote
Senior Level
$150K/yr - $200K/yr
5+ years exp
Faeth Therapeutics is a clinical-stage oncology company focused on advancing innovative therapies. The Senior Clinical Scientist will lead the design, execution, and interpretation of clinical trials, ensuring high-quality data delivery and driving cross-functional collaboration within the Clinical Development team.
BiotechnologyHealthcareHealth CareMedicalTherapeutics
No H1B
Responsibilities
Lead the design and development of clinical protocols, amendments, and core study documents (e.g.,IBs, DSURs, SAPs, CRFs)
Lead ongoing review, monitoring, querying and interpretation of clinical data (safety, efficacy, PK/PD, and biomarker endpoints)
Provide leadership across one or more clinical programs, including lifecycle planning
Oversee execution of Phase 1–3 clinical trials in partnership with Clinical Operations, ensuring quality, timelines, and clinical review of data
Serve as a primary clinical point of contact for CROs, vendors, and investigative sites
Identify and proactively mitigate study risks; drive issue resolution across functions
Drive data quality, including oversight of data cleaning, query resolution, and database lock
Ensure alignment between clinical strategy and translational/biomarker plans
Lead contributions to regulatory submissions (INDs, CTAs, briefing documents, responses to health authorities)
Drive preparation of clinical study reports (CSRs), abstracts, manuscripts, and conference presentations
Represent Clinical Development in internal governance meetings and external interactions
Qualification
Oncology clinical developmentInterventional clinical trials Phase 1–3Clinical trial designClinical trial executionClinical data interpretationOncology drug developmentMetabolismNutritionBiomarker-driven approachesClinical Practice (GCP)ICH guidelinesGlobal regulatory requirementsAnalytical skillsInfluence without authorityCross-functional leadership
Required
5–8+ years of oncology clinical development experience
Demonstrated experience leading components of interventional clinical trials (Phase 1–3)
Strong expertise in clinical trial design, execution, and data interpretation
Deep understanding of oncology drug development; experience in metabolism, nutrition, or biomarker-driven approaches is a plus
Working knowledge of GCP, ICH guidelines, and global regulatory requirements
Proven ability to lead cross-functional initiatives and influence without authority
Excellent communication, analytical, and problem-solving skills
Comfortable operating in a fast-paced, evolving biotech environment
Preferred
Advanced degree (PhD, PharmD, MS, or equivalent) in life sciences, clinical research, or related field
Benefits
Competitive salary and equity in a well-funded, clinical-stage biotech
100% remote work and flexible schedule
Health, dental, and vision for you and your dependents
Flexible time off
Generous parental leave
Traditional and Roth 401k
Mission oriented, remote first culture
Company
Funding
Current Stage
Early StageTotal Funding
$92MKey Investors
S2G InvestmentsFuture Ventures,Khosla Ventures
2026-02-18Acquired
2025-10-20Series A· $25M
2022-06-30Series A· $47M
Recent News
Pharmaceutical Technology
2026-08-19
MarketScreener
2026-08-17
Company data provided by crunchbase