IR
Integrated Resources, Inc.
Research Scientist

Clinical Research Scientist

On-siteMidResearch Scientistposted 111mo ago
Role summaryAI-generated

This role bridges clinical research and data science, requiring expertise in designing, executing, and analyzing Phase I-III trials while ensuring compliance with regulatory standards. The ideal candidate will leverage statistical methods and documentation skills to support evidence-based decision-making in pharmaceutical or biotech settings.

Skills required

About this role

Title: Clinical Research Scientist
Duration: 12 Months (Possibility of Extension)
Location Woodcliff lake NJ


Job Responsibilities:

  • The incumbent is responsible for, but not limited to the following:
  • Assist in the planning, implementation, managing, and reporting of Phase I-III clinical studies
  • Prepare and review project and study documents including clinical trial protocols, clinical study reports, patient SAE narratives, clinical sections of registration dossier documents (ISS, ISE, Investigator Brochure, etc)
  • Performs literature search and data analysis to address research questions
  • In collaboration with other clinical staff and/or an external CRO, monitoring clinical trial conduct (enrollment, GCP practices, handling of safety issues, etc.)
  • Assisting in database cleaning, review of study results, and interpretation of results
  • Adhering to key performance indicators for clinical study development, conduct, and reporting
  • Individual contributor with specialized knowledge
  • Presents concepts, facts, and reports and advises on key trends and issues
  • Troubleshooting routine site inquiries
  • Work is completed under limited supervision
  • Supports the planning, execution and reporting of clinical programs/trials
  • May handle multiple protocols simultaneously
  • Contributes to risk resolution by escalating and monitoring project risks

Qualifications

Qualifications

  • Minimum of 2-5 years of experience in clinical research in the pharmaceutical industry
  • A thorough understanding of clinical research methodology including study design, protocol writing, and CRF preparation is required, as is a knowledge of GCP and local regulatory requirements
  • Working knowledge of the IND/NDA/CTD/MAA process acquired through direct industrial experience preferred
  • Knowledge of medical, scientific and clinical research techniques in the oncology therapeutic area;
  • Bachelor’s Required. Doctoral (PharmD or PhD) or MD degree preferred.

Additional Information

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral bonus

Thank you for your time and consideration. I look forward to hearing from you!

Kind Regards

Ruchi Kumari

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I

(DIRECT BOARD) # 732-844-8716 (F) 732-549-5549

LinkedIn: https://www.linkedin.com/in/ruchi-kumari

Gold Seal JCAHO Certified ™ for Health Care Staffing

“INC 5000’s FASTEST GROWING, PRIVATELY HELD COMPANIES” (8th Year in a Row)

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