Senior Clinical Research Associate - Obesity - Central U.S. (Remote)
About The Position
We are Worldwide Clinical Trials, a global, midsize CRO that pushes boundaries and innovates to find cures for persistent diseases. Our mission is to work with passion and purpose every day to improve lives. In Clinical Operations, you will contribute to patient well-being by working alongside brilliant minds across diverse therapeutic areas. We foster a supportive, team-oriented environment where collaboration and creativity are encouraged. As a CRA, you will receive extensive support for regulatory submissions, TMF management, and in-house CRAs for projects with heavy site management needs. We prioritize professional development through regular touchpoints and coaching, offering a clear career path that can lead to Clinical Trial Manager roles. Our accessible Executive Leadership team is committed to advancing science and overcoming obstacles to improve patients' lives worldwide. You will drive scientific breakthroughs and be at the core of every successful clinical trial.
Requirements
- 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
- 5+ years of experience as a Clinical Research Associate
- 4-year university degree OR Nursing Degree
- Experience in Obesity or Metabolic Disease required
- Candidates must reside in the Central United States
- Willingness to travel regionally required
Nice To Haves
- Rare Disease experience is a plus but not required
Responsibilities
- 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
Benefits
- Competitive benefits package depending on location
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What This Job Offers
Job Type
Full-time
Career Level
Senior
Education Level
Associate degree
