Contractor, Clinical Research Scientist

Aequor-a6ad214d; Princeton (NJ); Hybrid; USD 120,000 - 160,000; Part time

Job summary

Aequor-a6ad214d is seeking a hands-on Clinical Research Scientist (Oncology/Hematology) for a 6-month contract in Princeton, NJ or Pleasanton, CA. The role is hybrid (3 days on-site Tue–Thu) and focuses on day-to-day clinical trial execution, data cleaning, and scientific document authoring.

Qualifications include an MS or PhD in Life Sciences or related field, 3–5 years of drug development experience, and strong oncology expertise with hematology exposure preferred.

Qualifications

• Requires advanced degree (MS or PhD) in Life Sciences, Oncology, Pharmacology, or related field.
• 3–5 years of drug development experience in pharma/biotech.
• Hands-on experience with EDC listings, data cleaning, and core clinical document generation.

Responsibilities

• Draft and contribute to study protocols, CSRs, IBs, DSURs, NDA/MAA submissions and publications.
• Review and summarize clinical data (EDC and listings) to monitor quality and ensure clean data flow.
• Critically evaluate efficacy, safety, and biomarker data to support risk assessments and milestones.
• Collaborate with Medical Directors, Clinical Operations, Data Management, Biostatistics, and Medical Writing to keep trials on track.

Skills

Clinical data review

Data cleaning

Scientific writing

Cross-functional collaboration

Education

MS/PhD in Life Sciences / Oncology / Pharmacology

Tools

EDC listings

Clinical data management systems

Job description

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

Overview
Seeking 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 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: 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).
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