Senior Clinical Scientist

Atrium Therapeutics • San Diego, CA

4d

About The Position

Atrium Therapeutics is seeking a Senior Clinical Scientist to work with internal stakeholders on developing and executing clinical development plans and clinical trials. In support of the Global Development Lead and cross-functional program teams, this role contributes to the analysis and interpretation of safety and efficacy data, supports regulatory submissions and scientific communications, and helps achieve program goals and milestones in compliance with applicable regulations and ICH/GCP.

Requirements

• Advanced degree: PhD, MD, or PharmD.
• At least 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.
• 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 work in a deadline-driven environment, support multiple projects simultaneously, and work effectively on cross-functional teams.

Nice To Haves

• Publication, peer-review, or scientific conference presentation experience.

Responsibilities

• Contribute to planning and designing 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 in a timely manner, including training related to security, regional data protection requirements, GxP, and SOPs.

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, including job-specific industry training.
• Education reimbursement program.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree