Senior Clinical Research Associate - Metabolic - Central
Worldwide Clinical Trials · Virtual United States Oklahoma +1 more
Clinical OperationsFull-timeCompany career page
The apply link worked recently (not employer-confirmed).
Role summary
Senior Clinical Research Associate position focused on metabolic disease studies within a global CRO. The role involves managing site activities across the clinical trial lifecycle, including study initiation, regulatory compliance, and safety reporting, with a primary remote structure and regional travel requirements.
What they're looking for
- 5+ years of experience as a Clinical Research Associate
- 4-year university degree or nursing degree
- Experience in metabolic disease research; obesity experience preferred
- Proficiency in Microsoft Office, CTMS, and EDC systems
- Excellent written and oral communication skills in English
- Superior organizational skills with strong attention to detail
- Ability to work independently with minimal supervision
What you'll be doing
- Manage research activities and site compliance across participating clinical research sites
- Conduct study initiation visits and oversee study startup activities including regulatory document collection
- Support site training on data collection procedures and adverse event reporting protocols
- Monitor site activities during study maintenance and coordinate closeout procedures
- Ensure adherence to informed consent processes and regulatory requirements
Compensation$97,000.00 - $193,000.00 annually
Key requirements
- Therapeutic area
- Metabolic
Privacy & handoff
This role links to Worldwide Clinical Trials's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.