Job Details

  • Title: CS3 Associate Contractor
  • Code: RCI-33048/33049
  • Location: Lawrenceville New Jersey (NJ) 08648
  • Posted Date: 09/28/2020
  • Duration: 12 Months
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  Job Description

  • BA/BS Degree, BA/BS Degree or LPN
  • 4 or more years of experience in clinical research, with minimum of 2 years of that experience at a pharmaceutical company or CRO, including participation in data management and pharmaceutical safety reporting.
  • Experience working in clinical operations or safety surveillance role, demonstrating knowledge of project, protocol, site, data management, clinical/medical review, and signal detection and assessment.
  • Knowledge and understanding of the conduct and management of international clinical trials, particularly data collection processes from both clinical and data management perspectives.
  • Established experience working in a team environment within a matrix organization.
  • Works well across organizational, functional, and geographic boundaries to achieve company goals.
  • Excellent oral, written, and interpersonal communication skills.
  • Demonstrated attention to detail and strong organizational skills.
  • Well-developed project management and leadership skills, including prioritization methods.
  • Knowledge and understanding of safety surveillance, risk management, and signal assessment capabilities and appreciation of overall R&D organizations (e.g., how they operate, key business drivers, etc.)
  • Strong knowledge of safety reporting, medical conditions/diseases, ICH/GCP Guidelines, and REMS/RMP.
  • Working knowledge of computer applications including Microsoft Office Suite, Oracle based systems, Trial Management systems, electronic data capture (TAO & RAVE), MedDRA library, J-Review
  • Speed
  • Innovation
  • Passion
  • Accountability