Clinical Research Scientist (Oncology / Hematology)

Aequor; Princeton (NJ); Hybrid; USD 120.000 - 170.000; Teilzeit

Zusammenfassung

Aequor is seeking a hands-on Clinical Research Scientist (Oncology/Hematology) for a long-term contract in Princeton, NJ. This hybrid role requires on-site presence Tue–Thu and involves leading trial execution, data cleaning, and cross-functional collaboration.

You will author essential study documents, review clinical data listings, and interpret efficacy and safety signals to support milestones and regulatory submissions. A strong oncology background is essential.

Qualifikationen

• Advanced degree (MS or PhD) in Life Sciences or related field.
• 3–5 years drug development experience in pharma/biotech.
• 2+ years Oncology, Hematology-Oncology preferred.
• Hands-on data cleaning and core clinical document generation.
• Local to Princeton, NJ or Pleasanton, CA with 3 days on-site Tue-Thu.

Aufgaben

• Clinical Document Authoring: draft protocols, CSRs, IBs, DSURs, regulatory submissions, and publications.
• Hands-on Data Review & Cleaning: review EDc data listings, ensure data quality and protocol compliance.
• Clinical Data Interpretation: evaluate efficacy, safety, and biomarker data to support risk assessments.
• Cross-Functional Collaboration: partner with Medical Directors, Clinical Operations, Data Mgmt, Biostatistics, and Medical Writing.

Kenntnisse

Oncology expertise

Hematology-Oncology

Data cleaning

Clinical document generation

EDC data review

Cross-functional collaboration

Ausbildung

MS or PhD in Life Sciences / Oncology / Pharmacology

Tools

EDC systems

Jobbeschreibung

Clinical Research Scientist (Oncology / Hematology)

Long Term Contract

Princeton, NJ

Hybrid - 3 Days On-Site (Tuesday - Thursday)

About the Company:

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 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).