Worldwide Clinical Trials

Senior Clinical Research Associate - Oncology - East Coast - Remote

Worldwide Clinical Trials • $90K — $120K *
Research Triangle Park, NC 27709In-Person
Pharmaceuticals & Biotech
5 - 7 years of experience
1 week ago
Job Overview by Ladders

Qualifications

  • 5+ years of experience as a Clinical Research Associate
  • 4-year university degree OR Nursing Degree
  • Experience in Oncology is required
  • Candidates must reside on the East Coast, United States
  • Willingness to travel regionally required

Responsibilities

  • Manage research activities at clinical trial sites
  • Identify potential sites for research participation
  • Perform study start-up activities, including regulatory document collection
  • Support negotiation of contracts and budgets with sites
  • Train sites on data collection and safety reporting
  • Conduct study initiation visits (SIVs)
  • Ensure compliance with informed consent and regulatory standards

Benefits

  • Opportunity to impact patients' lives positively through research
  • Work in a leading clinical research environment
  • Gain experience managing end-to-end clinical studies
  • Collaborate with diverse teams across multiple sites
Full Job Description
What you will do
  • Responsible for managing the research activities at sites participating in Worldwide's clinical research projects
  • 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
  • Conduct study initiation visits (SIVs)
  • While most of the site management efforts will be performed remotely, you will be required to ensure compliance with obtaining informed consent, reporting potential safety-related events, and adhering to all applicable regulatory requirements


What you will bring to the role
  • Excellent interpersonal, oral, and written communication skills in English
  • Superior organizational skills with attention to detail
  • Ability to work with little or no supervision
  • Proficiency in Microsoft Office, CTMS, and EDC Systems


Your experience
  • 5+ years of experience as a Clinical Research Associate
  • 4-year university degree OR Nursing Degree
  • Experience in Oncology is required
  • Candidates must reside on the East Coast, United States
  • Willingness to travel regionally required


We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

About Worldwide Clinical Trials

Worldwide Clinical Trials is a global contract research organization (CRO) that provides clinical research services to pharmaceutical and biotechnology companies. They specialize in early phase development, late phase development, and full-service clinical research. Worldwide Clinical Trials has experience in a wide range of therapeutic areas, including oncology, neuroscience, and infectious diseases. They are committed to providing high-quality, efficient, and cost-effective services to their clients.
Learn more about Worldwide Clinical Trials
Size
1,500 employees
Industry
Healthcare
Founded
1986
* Ladders Estimates

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