Job Specifications
Senior Manager, Clinical Scientist – Data Reviewer
United States | Hybrid Jersy City
Oncology | Late-Stage Clinical Development
We are partnering with a well-funded, fast-growing oncology biotechnology company that is advancing a differentiated pipeline of transformative cancer therapies. As the organization continues to scale its clinical development function, they are hiring a Senior Manager-level Clinical Scientist (Data Reviewer) to play a pivotal role across safety data review, trial execution, and regulatory-ready evidence generation.
This is a high-impact, cross-functional role offering meaningful scientific ownership, visibility, and future leadership opportunity.
The Opportunity
In this role, you will act as a core scientific contributor across one or more clinical programs, with primary responsibility for end-to-end safety data review from study start-up through final Clinical Study Report (CSR). You will collaborate closely with Clinical Research, Pharmacovigilance, Clinical Operations, Biostatistics, and Regulatory to ensure data integrity, patient safety, and high-quality scientific output.
Key Responsibilities
Lead ongoing and ad-hoc safety data review activities across clinical trials from initiation through final CSR
Interpret and analyze clinical trial data to ensure accuracy, integrity, and regulatory compliance
Contribute to protocol development, study design, and scientific planning activities
Partner with Pharmacovigilance on safety signal identification, evaluation, and documentation
Support data review meetings, internal safety discussions, and cross-functional governance forums
Contribute to clinical documents, including CSRs, IBs, protocols, and regulatory submissions
Serve as a trusted scientific voice within the clinical development team
Identify opportunities to improve processes, drive efficiencies, and support team growth
Who We’re Looking For
Advanced scientific degree (PhD, PharmD, MD, or equivalent) in a life-science discipline
Strong experience in clinical science or clinical data review, ideally within oncology
Proven background supporting clinical trials across multiple phases
Deep understanding of clinical safety data, adverse event review, and regulatory expectations
Highly collaborative, detail-oriented, and data-driven mindset
Comfortable operating in a fast-moving biotech environment with increasing responsibility
Prior leadership or mentoring experience is a plus, with clear runway for growth
Why Join
Join a high-caliber oncology organization with strong financial backing and a compelling pipeline
High visibility role with real influence on clinical strategy and patient outcomes
Collaborative culture with strong scientific leadership
Competitive compensation and long-term growth potential
About the Company
SciPro (formerly Lawrence Harvey Life Sciences) is a people business. We specialise in sourcing, advising and introducing highly skilled life sciences candidates to our client partners across the globe, helping them to achieve their business goals. We provide talent on an executive level, contract, permanent and retained basis to SME, big Pharma businesses and incorporating CRO's and consultancies across the Pharmaceutical, Biotech and Medical Device industries. Our consultants are technically aligned specialists focusing on...
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