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Clinical Research Scientist

Job in Summit, Union County, New Jersey, 07902, USA
Listing for: Real Staffing
Full Time position
Listed on 2026-02-28
Job specializations:
  • Research/Development
    Clinical Research
  • Healthcare
    Clinical Research
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Real Staffing Group is a global staffing and recruitment specialist providing contract and permanent talent to a wide range of companies and industries. We take time to understand your career ambitions, working with you and for you at every stage of your job search. By applying our industry knowledge to your specific requirements we aim to supply you with the most effective route to your new career opportunity.

To find out more about Real Staffing Group please visit

Job Description

CORE

JOB RESPONSIBILITIES:

  • Assist the Clinical Research team to interface with project team members including:
    Clinical Research Physician, Clinical Operations, Data Management, Statistics, Drug Safety, Regulatory and Project Management.
  • Review and query of hematology/oncology data including: safety, primary efficacy variables, and laboratory data.
  • Assist with protocol preparation (writing, reviewing, amending and cross-functional facilitation as appropriate).
  • Assist with clinical study report preparation to include narrative writing
  • Participate in adhoc meetings
Qualifications
  • Advanced Degree in Life Sciences (e.g., nursing, pharmacy or related medical field), minimum 5 years’ experience in clinical research development or equivalent
  • Oncology experience REQUIRED. Hematology experience is a plus. Protocol authoring is a plus. Data review and medical monitoring of data REQUIRED.
  • Minimum 5 yrs experience in oncology clinical development
  • Excellent written and verbal communication skills and interpersonal skills.
  • Knowledge of clinical trial design, basic statistics, and data review tools
  • Experience in protocol development, study report preparation, Investigator Brochure preparation, regulatory submissions
  • Full understanding GCP and ICH Guidelines
  • Detail-oriented, well-organized
  • Ability to assimilate technical and scientific information quickly
  • Proficient in Microsoft Office (Word, Excel, PowerPoint; Microsoft project a plus), JReview, EDC (Rave)
  • Demonstrated ability to work as part of a team
Additional Information

All your information will be kept confidential according to EEO guidelines.

IF THIS IS THE JOB OPPORTUNITY FOR YOU GIVE ME A CALL AT  ASAP!

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