Position Summary:
Atrium Therapeutics is seeking a Senior Clinical Scientist to work with key internal stakeholders on the development and execution of 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, publications, and presentations; and helps achieve program goals and milestones in compliance with applicable regulations and ICH/GCP.
Job 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 the 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 all training requirements, including relating to security, regional data protection requirements, GxP and SOPs in a timely manner.
Education and Experience Requirements:
• Advanced degree required (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; publication, peer-review, or scientific conference presentation experience.
• 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.
What We Provide:
• The base salary range for this role is $185,000-$205,000. The final compensation will be commensurate with such factors as relevant experience, skillset, internal equity and market factors.
• Atrium offers competitive compensation and benefits which include stock options & RSUs, as well as a 401(k) with an employer match. In addition, the comprehensive wellness program includes coverage for medical, dental, vision, LTD, and unlimited of time off including summer & winter breaks.
• A commitment to learning and development which includes a variety of programming internally developed by and for Atrium employees, opportunities for job-specific training offered by industry, and an education reimbursement program.
$185,000 - $205,000 a year
