Senior Clinical Research Scientist

ApTask Global Workforce

Plainsboro Township (NJ)

Remote

USD 96,000 - 160,000

Full time

3 days ago
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Job summary

Aptask Global Workforce (AGW) seeks a Senior Clinical Research Scientist to lead or co-lead oncology-focused clinical trials in a remote role for a global biotechnology company based in Plainsboro, NJ.

The position requires 10+ years in clinical research with 3+ years in oncology drug development; strong data review experience; and the ability to thrive in a matrixed, fast-paced environment. Contract opportunity with competitive hourly pay.

Qualifications

  • PhD, PharmD, MS or equivalent degree in medical/biological/pharmaceutical field.
  • 10+ years clinical research experience with at least 3+ years in oncology drug development.
  • Experience with data review and oncology solid tumors.
  • Experience in a project-oriented matrixed team environment.
  • Proven ability to work under pressure with tight timelines.

Responsibilities

  • Lead or co-lead clinical trials across development stages.
  • Develop program strategy and CDP for assigned trials/compounds.
  • Prepare clinical/regulatory documents and safety updates.
  • Support eCRF development and data management deliverables.
  • Mentor junior scientists and present at meetings.

Skills

Oncology experience
Data review
Team collaboration
Matrixed environment
Under pressure
Clinical research leadership

Education

PhD or equivalent

Tools

eCRF development
MDRP data review

Job description

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.

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

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.

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