Previous Job
Previous
Clinical Research Scientist
Ref No.: 18-50826
Location: Woodcliff Lake, New Jersey
Position Type:Contract
Start Date / End Date: 09/17/2018 to 03/16/2019
Job Title: Clinical Research Scientist
Location: Woodcliff Lake, NJ
Duration: 06 Months
Job ID: EZIJP00002796
Position Type: Contract Role
Client: A Big Pharmaceutical Company


Job Description:
This will be a 6 months contract for now , with the possibly to extend
Open to remote work 1 day a week. May be flexible with more once worker started and a relationship/trust is built.

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, Client, 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 (enrolment, 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.
Skills & Required Experience:
  • 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.
  • 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.
Therapuetic Area & Education:
  • Knowledge of medical, scientific and clinical research techniques in the oncology therapeutic area.
  • Bachelor's Required.
  • Doctoral (PharmD or PhD) or MD degree preferred.
Interested candidates can share their most updated resume at wajid.khan@artech.com or they can reach out to me on #973-967-3412