Clinical Research Scientist (Oncology / Hematology)
Aequor · Princeton, New Jersey, United States
FULL TIMEpermanent
Job Description
Clinical Research Scientist (Oncology / Hematology)6-Month ContractPrinceton, NJ or Pleasanton, CAHybrid — 3 Days On-Site (Tuesday – Thursday)
If you are considering sending an application, make sure to hit the apply button below after reading through the entire description.
OverviewSeeking 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 ResponsibilitiesClinical 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.
RequirementsEducation: 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. xzbcwsv Logistics: Must be local to Princeton, NJ or Pleasanton, CA and committed to the 3-day/week on-site schedule (Tue–Thu).
If you are considering sending an application, make sure to hit the apply button below after reading through the entire description.
OverviewSeeking 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 ResponsibilitiesClinical 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.
RequirementsEducation: 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. xzbcwsv 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, United States |
| Type | FULL TIME |
| Niche | hr |
| Experience | permanent |