Job Overview:

The SCRP is a Medically Qualified person without or with limited experience in a drug development/drug safety environment or medical data review. SCRP works together under supervision of Medical Director or other experienced medical staff in medical monitoring, study design, and regulatory agency interactions.

Activities provided by SCRP include advisory support of medical nature with the aim to ensure the safety and well-being of study participants, integrity of the project data in accordance with the clinical trial protocol/clinical study protocol (or equivalent documents), standard operating procedures (SOPs), good clinical practice (GCP), and all other applicable directives and regulatory requirements. Responsibilities of SCRP include medical inputs of assigned projects (e.g., clinical trial, clinical study, Non-Interventional Study, Registry study, etc.) from both a medical and scientific perspective. SCRP provides and/or oversees medica...