Oncology Clinical Research Scientist (Hematology) - Hybrid

International Society on Thrombosis and Hemostasis; Princeton (NJ); Hybrid; USD 83,000 - 124,000; Part time

Job summary

International Society on Thrombosis and Haemostasis seeks a hands-on Clinical Research Scientist with strong Oncology expertise to drive day-to-day clinical trial execution, data cleaning, and document authoring. The role is a six-month contract based in Princeton, NJ or Pleasanton, CA with a hybrid schedule of three on-site days (Tue–Thu).

You will collaborate with Medical Directors, Clinical Operations, Data Management, Biostatistics, and Medical Writing to advance trial milestones while

Qualifications

• MS or PhD in Life Sciences, Oncology, Pharmacology, or related field.
• 3–5 years of drug development experience in pharma/biotech.
• 2+ years in Oncology; Hematology-Oncology preferred.
• Hands-on experience with EDC listings, data cleaning, and document generation.

Responsibilities

• Clinical Document Authoring: Draft and contribute to study protocols, CSRs, IBs, DSURs, NDA/MAA submissions, and publications.
• Hands-on Data Review & Cleaning: Review and summarize ongoing clinical data (EDC and data listings) to monitor study quality, resolve queries, ensure clean data flow and protocol compliance.
• Clinical Data Interpretation: Critically evaluate and interpret efficacy, safety, and biomarker data to support risk assessments and study milestones.
• Cross-Functional Collaboration: Partner with Medical Directors, Clinical Operations, Data Management, Biostatistics, and Medical Writing to keep trials on track.

Skills

3-5 years drug development experience

Oncology experience

Hematology-Oncology exposure

Clinical Document Authoring

Data review & cleaning

Education

MS or PhD in Life Sciences / Oncology / Pharmacology

Tools

EDC listings tools

CSR/IB drafting tools

Job description

International Society on Thrombosis and Haemostasis seeks a hands-on Clinical Research Scientist with strong Oncology expertise to drive day-to-day clinical trial execution, data cleaning, and document authoring. The role is a six-month contract based in Princeton, NJ or Pleasanton, CA with a hybrid schedule of three on-site days (Tue–Thu).

You will collaborate with Medical Directors, Clinical Operations, Data Management, Biostatistics, and Medical Writing to advance trial milestones while