Senior Clinical Scientist
Atrium Therapeutics•San Diego, CA
•$185,000 - $205,000
About The Position
Atrium Therapeutics is seeking a Senior Clinical Scientist to work with internal stakeholders on developing and executing clinical development plans and trials. In support of the Global Development Lead and cross-functional program teams, the role contributes to the analysis and interpretation of safety and efficacy data, supports regulatory submissions, publications, and presentations, and helps achieve program goals and milestones in compliance with applicable regulations and ICH/GCP.
Requirements
- Advanced degree (PhD, MD, or PharmD).
- Minimum of 8 years of relevant experience, including at least 3 years of clinical science experience in a pharmaceutical or biotechnology environment.
- Rare disease and/or cardiology experience.
- Expert knowledge of scientific principles and concepts.
- Experience with publication, peer review, or scientific conference presentations.
- Knowledge of clinical trial design; ability to assimilate technical and scientific information; and proficiency in data analysis and interpretation.
- Experience contributing to clinical and regulatory documents.
- Excellent interpersonal, written and verbal communication, presentation, organizational, and workload-prioritization skills.
- Ability to perform in a deadline-driven environment, support multiple projects simultaneously, and work effectively on cross-functional teams.
Responsibilities
- Contribute to the planning and design of clinical studies in accordance with corporate objectives.
- Provide scientific support through literature searches, interpretation of scientific literature, and evaluation of technologies that aid clinical strategy, study implementation, and due diligence.
- Contribute to clinical oversight and scientific review of trial data, including analysis and interpretation of efficacy and safety data.
- Support the Study Medical Monitor in tracking laboratory results and communicating with site staff.
- Collaborate with Clinical Operations to translate protocols into operational deliverables, review study data, and prepare or review study plans.
- Draft, review, and revise clinical documents, including protocols, clinical study reports, informed consent forms, investigator brochures, annual reports, and regulatory submission materials.
- Contribute to cross-functional and clinical meetings, including study team, investigator, site initiation, ad hoc, and steering committee meetings.
- Complete required training relating to security, regional data protection requirements, GxP, and SOPs in a timely manner.
Benefits
- Stock options and RSUs
- 401(k) with employer match
- Medical, dental, vision, and LTD coverage
- Unlimited time off, including summer and winter breaks
- Learning and development programming
- Job-specific industry training opportunities
- Education reimbursement program
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
Ph.D. or professional degree
