Contractor, Clinical Research Scientist

Aequor • Princeton, NJ

4d • Hybrid

About The Position

Seeking a hands-on Clinical Research Scientist with strong oncology expertise, preferably in hematology, to drive day-to-day clinical trial execution. The role combines scientific document authoring with hands-on clinical data cleaning and review across ongoing studies. This is a six-month contract role based in Princeton, New Jersey, or Pleasanton, California, with a hybrid schedule requiring on-site work three days per week, Tuesday through Thursday. Candidates must be local to one of these locations and committed to the on-site schedule.

Requirements

• 3–5 years of drug development experience in pharma or biotech.
• At least 2 years of oncology experience.
• Hands-on experience with EDC listings, clinical data cleaning, and core clinical document generation.
• Must be local to Princeton, NJ, or Pleasanton, CA, and able to work on-site three days per week, Tuesday through Thursday.

Nice To Haves

• An advanced degree (MS or PhD) in Life Sciences, Oncology, Pharmacology, or a related field is strongly preferred.
• Hematology-Oncology experience is strongly preferred.

Responsibilities

• Draft and contribute to study protocols, Clinical Study Reports (CSRs), Investigator Brochures (IBs), DSURs, NDA/MAA regulatory submissions, and scientific publications.
• Review and summarize ongoing clinical data from EDC and data listings to monitor study quality, resolve queries, and ensure clean data flow and protocol compliance.
• Evaluate and interpret clinical efficacy, safety, and biomarker data to support risk assessments and study milestones.
• Collaborate with Medical Directors, Clinical Operations, Data Management, Biostatistics, and Medical Writing to keep clinical trials on track.

What This Job Offers

• Career Level: Mid Level