Senior Clinical Scientist

Atrium Therapeutics

. Work with key internal stakeholders on the development and execution of clinical development plans and clinical trials .

Posted 10/30/2026full-timeSan Diego • California • United StatesSenior💰 $185,000 - $205,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial design, regulatory submissions, and data analysis within the pharmaceutical or biotechnology sectors. Proven ability to collaborate with cross-functional teams and communicate complex scientific information effectively.

Highest-signal resume keywords

Clinical Trial DesignRegulatory SubmissionsData Analysis and InterpretationScientific Literature InterpretationCross-Functional Collaboration

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Science ExperienceSafety and Efficacy Data AnalysisClinical Document DraftingPublication and Presentation ExperienceTechnology Evaluation

Soft Skills

Excellent Communication SkillsOrganizational SkillsWorkload PrioritizationInterpersonal Skills

Certifications & Qualifications

Advanced Degree (PhD, MD, or PharmD)

Industry Keywords

PharmaceuticalBiotechnologyRare DiseaseCardiologyGxPSOP Training

About the role

Key responsibilities & impact

Work with key internal stakeholders on the development and execution of clinical development plans and clinical trials
Support the Global Development Lead and cross-functional program teams
Analyze and interpret safety and efficacy data
Support regulatory submissions, publications, and presentations
Contribute to clinical study planning and design in accordance with corporate objectives
Provide scientific support through literature searches, scientific literature interpretation, and technology evaluation
Contribute to clinical oversight and scientific review of trial 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
Participate in cross-functional and clinical meetings
Complete required security, regional data protection, GxP, and SOP training

Requirements

What you’ll need

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
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

Benefits

Comp & perks

Stock options & RSUs
401(k) with an employer match
Wellness program
Medical coverage
Dental coverage
Vision coverage
LTD coverage
Unlimited time off, including summer & winter breaks
Learning and development programming
Job-specific industry training opportunities
Education reimbursement program