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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).
  
  #TechAM

Aptask Global Workforce (AGW) is seeking a Senior Clinical Research Scientist for a Remote position with a Pharmaceutical Company located in Plainsboro, NJ. This is a 5 month contract opportunity.

This role involves contributing to the implementation of a global development strategy by leading or co-leading clinical trials for compounds in various stages of development. The ideal candidate will have extensive experience in oncology and will work closely with the Medical Director and other cross-functional teams to ensure high-quality and timely deliverables.

Responsibilities:

• Contribute to the implementation of the global development strategy, leading or co-leading one or more clinical trials in a therapeutic area for one or more compounds in various stages of clinical development
• Contribute to the development of the program strategy for assigned trials/compounds and participate in the development of the clinical development plan (CDP)
• In collaboration with the Medical Director, contribute to the development of clinical and regulatory documents, annual safety updates, and registration dossiers (i.e., protocol, ICF, IB, annual safety updates, study reports, regulatory submissions)
• Participate in the development of case report forms (eCRFs), eCRFs completion guidelines, and provide scientific support for other key data management deliverables
• Lead the development of the medical data review plan (MDRP), perform ongoing data review, and summarize efficacy and safety data for interpretation/analysis
• Provide medical input for country/site selection, feasibility assessment and engage in KOL interaction
• Prepare charters and coordinate internal/external committee meetings including presentation preparation
• Participate in the development and review of study plans and serve as a liaison to project teams and CROs
• Provide input for the development of publications in coordination with Scientific Communications
• Prepare presentations for Investigator meetings, CRO/CRA training, SIVs as warranted
• Mentor junior level Clinical Research Scientists as required

Requirements:

• PhD, Pharm D, MS or equivalent degree preferably within the medical, biological, pharmaceutical science or related discipline
• Minimum 10+ years of experience in clinical research with at least 3 or more years of drug development experience in oncology
• Experience with data review and solid tumors
• Experience working in a project-oriented matrixed team environment
• Proven experience working in teams
• Ability to work successfully under pressure in a fast-paced environment and with tight timelines

Pay range: up to $116.20 per hour

Only candidates available and ready to work directly as Aptask Global Workforce (AGW) employees will be considered for this position.

If you have the described qualifications and are interested in this exciting opportunity, apply today!

Aptask Global Workforce (AGW)

ApTask Global Workforce (AGW) is a certified Minority and Veteran workforce solutions company. AGW delivers operational, clinical, lab and professional talent with a strong focus on healthcare and life sciences. The company supports clients with reliable staffing, program expertise and a commitment to quality, speed and consistent delivery.

Benefits of working with ApTask Global Workforce include:

• Medical
• Dental
• Vision
• Sick Pay (for applicable states/municipalities)

Our team stays close to the process and is here to guide you every step of the way. To learn more, please visit our website (url removed). 

ApTask Global Workforce is an Equal Opportunity Employer. Candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.

Aptask Global Workforce (AGW) is seeking a Senior Clinical Research Scientist for a Remote position with a Global Biotechnology Company located in Plainsboro, NJ. This is a 5+ month contract opportunity.

This role involves contributing to the implementation of the global development strategy by leading or co-leading clinical trials for one or more compounds in various stages of development. The ideal candidate will have extensive experience in oncology and will work closely with the Medical Director and other cross-functional teams to ensure high-quality and timely deliverables.

Responsibilities:

• Contribute to the implementation of the global development strategy, leading or co-leading one or more clinical trials in a therapeutic area
• Contribute to the development of the program strategy for assigned trials/compounds and participate in the development of the clinical development plan (CDP)
• Contribute to the development of clinical and regulatory documents, annual safety updates, and registration dossiers
• Participate in the development of case report forms (eCRFs), eCRFs completion guidelines, and provide scientific support for other key data management deliverables
• Lead the development of the medical data review plan (MDRP), perform ongoing data review, and summarize efficacy and safety data for interpretation/analysis
• Provide medical input for country/site selection, feasibility assessment and engage in KOL interaction
• Prepare charters and coordinate internal/external committee meetings including presentation preparation
• Participate in the development and review of study plans and serve as a liaison to project teams and CROs
• Provide input for the development of publications in coordination with Scientific Communications
• Prepare presentations for Investigator meetings, CRO/CRA training, and SIVs as warranted
• Mentor junior level Clinical Research Scientists as required

Requirements:

• PhD, Pharm D, MS or equivalent degree preferably within the medical, biological, pharmaceutical science or related discipline
• Minimum 10+ years of experience in clinical research with at least 3 or more years of drug development experience in oncology
• Experience with Data Review and Oncology Solid Tumors
• Experience working in a project-oriented matrixed team environment
• Proven experience working in teams
• Ability to work successfully under pressure in a fast-paced environment and with tight timelines

Pay range: up to $116.20 per hour

Only candidates available and ready to work directly as Aptask Global Workforce (AGW) employees will be considered for this position.

If you have the described qualifications and are interested in this exciting opportunity, apply today!

Aptask Global Workforce (AGW)

ApTask Global Workforce (AGW) is a certified Minority and Veteran workforce solutions company. AGW delivers operational, clinical, lab and professional talent with a strong focus on healthcare and life sciences. The company supports clients with reliable staffing, program expertise and a commitment to quality, speed and consistent delivery.

Benefits of working with ApTask Global Workforce include:

• Medical
• Dental
• Vision
• Sick Pay (for applicable states/municipalities)

Our team stays close to the process and is here to guide you every step of the way. To learn more, please visit our website (url removed). 

ApTask Global Workforce is an Equal Opportunity Employer. Candidates will receive consideration without regard to their race, color, religion, sex, sexual orientation, gender identity, national origin, disability or status as a protected veteran.