
Clinical Trial Coordinator
2 days ago
The Patient Recruitment Associate I is a vital role in supporting clinical trials by identifying and screening volunteers for studies.
- Key Responsibilities:
- Screen potential volunteers via phone using prepared questionnaires to determine preliminary eligibility for study participation.
- Schedule consent/screening appointments for volunteers who pass the initial phone interview.
- Use the company's database to contact previous volunteers and successfully recruit them for studies.
- Ensure all calls are answered promptly with exceptional customer service and professionalism.
- Conduct demographic and medical history phone interviews with volunteers using prepared questionnaires.
- Accurately record and review demographic information and medical history for all volunteers while maintaining strict confidentiality.
- Schedule volunteers for further screening and/or consent appointments if they meet the criteria.
- Perform administrative tasks, such as data entry and reporting, to support the recruitment process.
- Education:
- An Associate's or Bachelor's Degree in Life Sciences or a related field (e.g., Pharmacy, Nursing, Medical Technology, Biology, etc.).
This is an exciting opportunity to contribute to the advancement of medical research by working closely with our team to identify and recruit volunteers for clinical trials.
As a Patient Recruitment Associate I, you will be responsible for:
- Managing volunteer relationships and ensuring timely communication.
- Developing and implementing effective recruitment strategies.
- Collaborating with cross-functional teams to ensure smooth trial execution.
- Staying up-to-date on industry developments and regulatory requirements.
The ideal candidate will have excellent communication and interpersonal skills, with the ability to work in a fast-paced environment.
They will also have a strong understanding of life sciences and healthcare-related concepts, as well as experience working in a contact center setting.
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