Clinical Screening Coordinator
Centricity Research · Suffolk, VA · 3 wk ago
On-siteHealthcareInternship
About the role
We’re looking for a Clinical Screening Coordinator to lead research-related recruitment initiatives and ensure the enrollment of high-quality patients in accordance with Centricity Research recruitment guidelines. In this role, you’ll screen patients for participation in clinical research studies with a solid understanding of study protocols, including inclusion/exclusion criteria, relevant medications, and medical conditions.
Responsibilities
- Work on enrollment and retention initiatives with the Site Manager
- Problem solve and create contingency plans to optimize enrollment via recruitment initiatives
- Obtain and maintain computerized database of all ad callers
- Return all phone calls/email responses to interested patients within 24 - 48 hours
- Accurately complete recruitment tracking log and all applicable clinical trial management systems
- Identify appropriate study candidacy based on knowledge of sites’ recruiting and upcoming studies
- Complete database query reviews for study candidacy and conduct outbound calls for study interest
- Provide study metrics on a regular basis and provide ongoing feedback regarding outcome of recruitment initiatives
- Occasionally attend community lectures, health fairs or events to promote Centricity Research
- Promote clinical trials in the community through outreach events
- Complete Informed Consent and screening visits per study protocol and Centricity Research SOP
- Complete the source documents, case report forms, and data queries in a timely manner, accurately, and completely
- Assist the Central Recruitment, Research Operations and/or Investigators with any other tasks as required
Requirements
- Communicate clearly and comfortably with patients by phone, email, and in person
- Stay organized and pay attention to details, especially when managing multiple tasks like outreach, documentation, and scheduling
- Be curious about clinical research and excited to learn protocols, medical terminology, and research ethics
- Feel confident using everyday computer tools like spreadsheets, databases, and email, and be open to learning systems like CTMS or EMR
- Bring experience from a healthcare, research, or customer-facing role, or be ready to dive in and learn on the job
Qualifications
- Bachelor’s degree in a related field (e.g., biology, healthcare, or psychology)
- Experience in patient screening and recruitment
- Strong organizational and communication skills
- Knowledge of clinical research protocols and medical terminology
Skills
- Excellent verbal and written communication skills
- Ability to manage multiple tasks and prioritize effectively
- Proficiency in Microsoft Office Suite
- Basic understanding of electronic health records (EHR) and clinical trial management systems (CTMS)
Benefits
- Comprehensive health, dental, and vision insurance
- Enhanced Employee Assistance Program (EAP) – mental health support
- Flexible Paid Time Off (PTO) + paid holidays
- Continuing education reimbursement
- 401(k) / RRSP with company match and immediate vesting
Pay
TBD
Schedule
Full-time