Original listing text, shown exactly as published by the company.
Key Responsibilities
- Collaborate with cross-functional teams to develop clinical documents for trials with scientific rigor, such as protocol, investigator brochure, clinical study report, scientific publications/presentations, etc.
- Contribute scientific input and implementation into the study design and execution, including but not limited to selection of appropriate endpoints, patient populations, and study methodologies; site selection; investigator meetings; and study initiation activities
- Monitor the clinical trials for both quality and safety, ensuring adherence to protocols, timelines, and quality standards
- Analyze clinical trial data, interpret results, and provide scientific insights to guide decision-making
- Collaborate with data management and biostatistics to develop and validate data collection tools and ensure accurate and timely data capture
- Foster relationships with clinical investigators to gather insights, address scientific questions, and promote collaboration
- Stay current with scientific literature and advancements in immunology related to Apogee’s pipeline
- Collaborate with clinical operations, medical affairs, regulatory affairs, biostatistics, and other teams to ensure alignment of clinical strategies with overall program goals
Ideal Candidate
- Advanced degree in life science field (e.g., PhD, PharmD, or DVM)
- Must have 10 +years of experience in research, with 5+ years’ experience working in clinical development within the biotechnology or pharmaceutical industry preferred; focus on immunology and/or dermatology preferred
- Strong understanding of clinical trial design, execution, and data analysis
- Analytical mindset and ability to interpret complex scientific data
- Ability to manage multiple competing priorities with good planning, time management and prioritization skills
- Strong communication, technical writing, and presentation skills, with the ability to effectively convey scientific concepts to diverse audiences
- Proven ability to work in a cross-functional team environment
- Solid knowledge of Good Clinical Practice (GCP) and ethical guidelines governing clinical research
- Successfully exhibit Apogee’s C.O.R.E. values: Caring, Original, Resilient and Egoless
- Position requires approximately 35% travel including mandatory in-person attendance at Apogee All Hands meetings typically held twice per year. Travel is also required to attend key Phase 3 meetings, typically held at the Apogee San Francisco office. This position may also require US and international travel to clinical sites and/or medical conferences.
The anticipated salary range for candidates for this role will be $230,000-$260,000 / year. The final salary offered will depend on several factors, which may include, but is not limited to relevant years of experience, educational background, and geography.
