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Aequor · Princeton, New Jersey
Clinical Research Scientist (Oncology / Hematology)
Long Term Contract
Princeton, NJ
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.
Overview
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.
Key
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.
Advanced degree ( MS or PhD ) in Life Sciences, Oncology, Pharmacology, or a related field strongly preferred.
3–5 years
of drug development experience in pharma/biotech.
Therapeutic Expertise:
Minimum
2+ years
in
Oncology
(experience in
Hematology-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).
Details
| Company | Aequor |
| Location | Princeton, New Jersey |
| Type | FULL TIME |
| Niche | Full-time |