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Clinical Scientist – Contractor
Aura Biosciences. Conduct ongoing review and interpretation of clinical trial data, including safety, efficacy, study conduct, and data quality .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in clinical trial methodology, data interpretation, and scientific writing, with a strong focus on ocular oncology and oncology drug development. Proven ability to collaborate cross-functionally and communicate clinical insights effectively.
Highest-signal resume keywords
Clinical Trial MethodologyScientific WritingData InterpretationCross-Functional CollaborationRegulatory Requirements
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
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Hard Skills
Clinical ResearchData ReviewEfficacy Data AnalysisSafety Data AnalysisClinical Study ReportingRegulatory SubmissionsPatient ProfilesTables and Figures CreationStudy DesignClinical Development Plans
Soft Skills
Communication SkillsPresentation SkillsOwnershipTime ManagementCollaboration
Certifications & Qualifications
PhDPharmDODMSMPH
Industry Keywords
Ocular OncologyOncology Drug DevelopmentBiotechnologyPharmaceuticalsMedical DevicesGCPPhase 2 Clinical DevelopmentPhase 3 Clinical DevelopmentInterventional Clinical TrialsHealth Authority Interactions
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Conduct ongoing review and interpretation of clinical trial data, including safety, efficacy, study conduct, and data quality
- Identify emerging clinical trends, inconsistencies, and data issues and drive timely resolution cross-functionally
- Partner with Biostatistics and Data Management on data review plans, patient profiles, listings, tables, figures, data cleaning, and database lock activities
- Serve as a clinical-science resource for study teams and support high-quality study execution with Clinical Operations
- Contribute clinical and scientific input to clinical development plans, study design, and analysis approaches
- Author or contribute to protocols, amendments, clinical study reports, investigator brochures, regulatory briefing documents, health authority responses, and other clinical documents
- Evaluate emerging clinical data, scientific literature, and competitive programs to inform study and development strategy
- Ensure clinical data and scientific rationale are presented clearly, accurately, and consistently across deliverables
- Develop presentations of clinical data for study teams, internal governance, and external scientific audiences
- Contribute to abstracts, posters, presentations, manuscripts, and other scientific communications
- Maintain current knowledge of ocular oncology, ophthalmology, oncology drug development, and the relevant therapeutic landscape
- Collaborate across Clinical Development, Clinical Operations, Biostatistics, Data Management, Safety, Regulatory Affairs, and other functions
- Communicate clinical insights, risks, and recommendations clearly using a patient-focused, evidence-based perspective
- Help develop fit-for-purpose clinical-science processes for a growing biotechnology company
Requirements
What you’ll need- Advanced degree in a relevant scientific or health-related discipline (PhD, PharmD, OD, or equivalent) strongly preferred; candidates with an MS, MPH, or other relevant advanced degree and substantial clinical development experience may also be considered
- 3+ years of relevant experience in clinical research or drug development within biotechnology, pharmaceuticals, or medical devices
- Experience supporting the conduct, analysis, and reporting of interventional clinical trials
- Demonstrated ability to review and interpret clinical and scientific data and translate findings into clear conclusions and recommendations
- Strong understanding of clinical trial methodology, GCP, and relevant regulatory requirements
- Strong scientific writing, presentation, communication, and cross-functional collaboration skills
- Ability to take ownership, manage multiple priorities, and deliver high-quality work in a fast-paced, evolving environment
- Experience in ophthalmology, oncology, or rare disease drug development preferred
- Experience with Phase 2 and/or Phase 3 clinical development preferred
- Hands-on experience with efficacy and safety data review, including patient profiles, listings, tables, and figures preferred
- Experience contributing to regulatory submissions or interactions with health authorities is a plus
- Ability to travel domestically and internationally as required
- Must be physically located in the UK
- Must be authorized to work legally in the UK
Benefits
Comp & perks- Full time weekly hours (40 hours per week)
- Year-long contractor with possibility for extension and/or conversion depending on business need
- Remote role in the UK