Faeth Therapeutics is a clinical-stage oncology company listed on Nasdaq that recently raised $200M in funding. With a strong scientific foundation and a founding team that includes the discoverer of the PI3K pathway, we are advancing PIKTOR, a multi-node PI3K/AKT/mTOR inhibitor program, into late stage development. 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.
The Senior Clinical Scientist is a key scientific leader within the Clinical Development team, responsible for the design, execution, and interpretation of clinical trials across Faeth’s oncology programs. This individual will drive cross-functional collaboration, provide strategic input into clinical development plans, and ensure delivery of high-quality data to support regulatory and scientific objectives. The role requires deep scientific expertise, operational insight, and the ability to influence both internal and external stakeholders.
Reports to: CMO
Location: Remote (U.S.)
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
Requirements:
- 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
Compensation Range: $150,000 - $200,000 (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 vision 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 our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
All offers of employment are contingent upon satisfactory completion of a background check and verification of eligibility to work in the United States.
