Senior Clinical Research Associate - Us - Remote

Worldwide Clinical Trials

North Carolina, US
**
Manage research activities at sites
Study start-up activities
Train sites on data collection
** Worldwide Clinical Trials is seeking a Senior Clinical Research Associate for a remote position, focusing on managing clinical research activities. The ideal candidate should have over five years of experience in the field, demonstrating strong communication and organizational skills. **

Job Summary

  • Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects, which are predominantly registries and other types of non-interventional / observational studies.
  • Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded.
  • While most of the site management efforts will be performed remotely, will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirement.

Matching Summary

Match Score: 75

** Worldwide Clinical Trials is seeking a Senior Clinical Research Associate for a remote position, focusing on managing clinical research activities. The ideal candidate should have over five years of experience in the field, demonstrating strong communication and organizational skills. **

Skills & Requirements

Must-have

  • Manage research activities at sites
  • Study start-up activities
  • Train sites on data collection
  • Manage site activities during maintenance
  • Conduct study initiation visits

Nice-to-have

  • Pioneering, creative approaches
  • Values-driven culture
  • Collaborative and creative environment
  • Passion and purpose

Key Requirements

  • 5+ years of experience as a Clinical Research Associate
  • 4-year university degree or RN/BSN in Nursing
  • Proficiency in Microsoft Office, CTMS and EDC Systems
  • Excellent interpersonal, oral, and written communication skills
  • Superior organizational skills with attention to details
  • Ability to work with little or no supervision
  • Willingness to travel required

Work Rights

Not specified

Tailored Resume

Cover Letter