Contractor, Clinical Research Scientist

Clinical Research Scientist (Oncology / Hematology)
6-Month Contract
Princeton, NJ or Pleasanton, CA
Hybrid — 3 Days On-Site (Tuesday – Thursday)

Overview
Seeking a hands-onClinical Research Scientist with strongOncology expertise (Hematology preferred) to drive day-to-day clinical trial execution. This role combines high-level scientific document authoring with hands-on clinical data cleaning and review across ongoing studies.

Key Responsibilities

• Clinical Document Authoring: Draft and contribute to high-quality study protocols, Clinical Study Reports (CSRs), Investigator Brochures (IBs), DSURs, NDA/MAA regulatory submissions, and scientific publications.

• Hands-on Data Review & Cleaning: Actively review and summarize ongoing clinical data (EDC and data listings) to monitor study quality, resolve queries, and ensure clean data flow and protocol compliance.

• Clinical Data Interpretation: Critically evaluate and interpret clinical efficacy, safety, and biomarker data to support risk assessments and study milestones.

• Cross-Functional Collaboration: Partner closely with Medical Directors, Clinical Operations, Data Management, Biostatistics, and Medical Writing to keep trials on track.

Requirements

• Education: Advanced degree (MS or PhD) in Life Sciences, Oncology, Pharmacology, or a related field strongly preferred.

• Experience:3–5 years of drug development experience in pharma/biotech.

• Therapeutic Expertise: Minimum2+ years inOncology (experience inHematology-Oncology strongly preferred).

• Core Competencies: Demonstrated hands-on experience with EDC listings, clinical data cleaning, and core clinical document generation.

• Logistics: Must be local to Princeton, NJ or Pleasanton, CA and committed to the 3-day/week on-site schedule (Tue–Thu).
  
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