Medical Research Associate conducting clinical assessments and phlebotomy at ICON. Responsible for ensuring volunteer health and comfort during trials in a research environment.
About the role
- Senior Clinical Research Associate managing clinical trial sites for Parexel. Ensuring compliance, training site staff, and maintaining study integrity throughout the process.
Responsibilities
- Act as direct contact with assigned sites
- Assess and ensure overall integrity of study implementation and adherence to study protocol at clinical sites
- Build relationships with investigators and site staff
- Facilitate and support site with access to relevant study systems
- Evaluate site recruitment plans
- Perform on-site visits and conduct remote contacts as needed
- Ensure timely and accurate completion of project goals and update applicable trial management systems
Requirements
- Bachelor’s degree in life sciences or professional degree in life sciences such as nursing, pharmacy, medical background or equivalent
- Minimum 5 years relevant experience in clinical research site monitoring (preferably 3 years in Oncology)
- Demonstrated experience across site start-up, conduct, and close-out
- Experience collaborating on site contracts and budgets preferred
- Preferred therapeutic experience in Oncology, Vaccines, Internal Medicine or Infectious Diseases
- Global clinical trial experience preferred
Benefits
- Health insurance
- Career development opportunities
- Flexible working arrangements
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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