Clinical Scientist – Contractor

🔥 3 minutes ago

🇬🇧 United Kingdom – Remote

⏳ Contract/Temporary

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 12%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Aura Biosciences

WebsiteLinkedInAll Job Openings

51 - 200 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Aura Biosciences is a biotechnology company focused on developing innovative cancer treatments. It is currently enrolling patients in the global Phase 3 CoMpass trial to evaluate the safety and efficacy of belzupacap sarotalocan (bel-sar) for treating small choroidal melanoma. The company utilizes a novel Virus-Like Drug Conjugates (VDCs) platform to target various solid tumors, with an emphasis on ocular and urologic oncology. Aura Biosciences aims to create a new standard of care in cancer treatment by offering early intervention options that preserve patient vision and improve long-term outcomes. The company is actively involved in research and clinical trials to address cancers like choroidal melanoma and non-muscle-invasive bladder cancer.

📋 Description

• 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

• 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

• 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