Regional Clinical Research Associate

itoring activities in accordance with Teleflex procedures and applicable regulations to evaluate protocol compliance, data accuracy, and subject safety by review of regulatory documents, medical records, reported data, and device storage, if applicable.

Education/experience requirements include a Bachelor's or Graduate degree in life sciences, nursing, or other health-related disciplines. Minimum five years as a CRA in the medical device or pharmaceutical industry or with a CRO is required.

Specialized skills/other requirements include demonstrated aptitude and knowledge in relevant therapeutic areas, experience conducting monitoring activities for first in human, investigational device exemption, post-approval and/or post-market studies, strong compliance focus and understanding of current GCP/ICH guidelines and FDA regulations, current certification as a Certified Clinical Research Associate (CCRA) or current Certified Clinical Research Professional (CCRP), strong knowledge of medical terminology, ability to work independently in a regional area with minimal supervision, excellent organizational and problem-solving skills, excellent interpersonal skills, ability to interface and communicate effectively with internal and external collaborators including physicians, site research staff, project teams and management, ability to interact constructively in communication of adherence to protocol and regulatory requirements, and responsible for adequate and reasonable home office setup including dedicated desk space to accommodate work responsibilities and Teleflex-supplied equipment.

Travel required: 70%.