Med Info Spec I (Night Shift & Hybrid) – Clinical Trial Patient Screening | Registered Nurse or Pharmacist Required
Core
Screen and match patients to clinical trials, manage high-volume inbound/outbound interactions, and handle medical information inquiries and adverse event reporting for pharmaceutical/device products.
Role type
Clinical Trial Patient Screening Specialist (Registered Nurse or Pharmacist)
Builds
Clinical trial participant matching and medical information services for global pharmaceutical clients
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Clinical trial eligibility screening, patient matching, medical information inquiry handling, adverse event documentation, regulatory compliance knowledge, medical literature research
Preferred skills
Previous clinical research experience, fluency in a second language
Technologies
Standard office equipment, clinical trial databases, communication platforms
Responsibilities
Conduct eligibility screening and match participants to appropriate clinical trials and sites; Respond to technical and medical information inquiries via phone, email, and mail; Document adverse events and product complaints according to regulatory guidelines; Analyze caller questions and formulate accurate responses using approved resources; Maintain detailed knowledge of client products, SOPs, protocols, and GCPs; Resolve complex inquiries with internal and external client contacts.
