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Clinical Research Scientist With Hematology / Oncology

Full-time

Aequor

Clinical Research Scientist (Oncology / Hematology)
Long Term Contract
Hybrid — 3 Days On-Site (Tuesday – Thursday)

Our client is a global, research-driven biopharmaceutical company specializing in oncology and innovative cancer treatments , with its U.S. headquarters in Princeton, New Jersey.

They are looking for a hands-on Clinical Research Scientist with strong Oncology 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.

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.
Partner closely with Medical Directors, Clinical Operations, Data Management, Biostatistics, and Medical Writing to keep trials on track.

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.
Minimum 2+ years in Oncology (experience in Hematology-Oncology strongly preferred).
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).

Vacancy posted 1 day ago
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