Clinical Research Patient Recruiter
New
J
JobgetherClinical Research
Based in the United StatesFull-Time
Salary not disclosed
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Job Details
- Languages
- Fluent written and spoken English; Spanish-speaking capabilities are preferred.
- Required Skills
- Microsoft OfficeCanva
Requirements
- Prior experience in clinical research patient recruitment is required.
- High school diploma required; a bachelor's degree is preferred.
- Strong interpersonal and verbal and written communication skills, with the ability to establish rapport and communicate effectively with patients by phone.
- Strong organizational skills and the ability to manage multiple recruitment activities and maintain accurate records.
- Working proficiency with Microsoft Office applications.
- Experience using social media platforms such as Facebook, Instagram, and X for recruitment or outreach purposes.
- Familiarity with simple graphic design tools such as Canva.
- Ability to understand and apply clinical study protocols, eligibility criteria, medical terminology, and medication information.
- Strong attention to detail and commitment to maintaining patient confidentiality.
- Fluent written and spoken English; Spanish-speaking capabilities are preferred.
Responsibilities
- Review study protocols and develop a strong understanding of inclusion and exclusion criteria, diagnoses, medical terminology, and medication histories.
- Pre-screen patient records to determine eligibility and support appropriate placement into clinical studies.
- Match potential subjects with active or upcoming research studies based on their needs and study requirements.
- Conduct outbound recruitment calls, respond to inbound patient inquiries, and schedule research appointments.
- Build rapport with potential participants and provide a professional, supportive, and patient-focused experience throughout the recruitment process.
- Accurately enter and maintain potential subject information, recruitment status, screening outcomes, medical histories, and medication information in the clinical research database.
- Track and identify trends related to patient acceptance, interest, or disapproval of clinical trial participation.
- Create and schedule IRB-approved social media posts and mass emails promoting active research studies.
- Develop recruitment materials such as flyers, brochures, and other study-related communications.
- Maintain confidentiality when handling patient and medical information.
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