Job Description
📋 Description Independently perform, coordinate and oversee all aspects of the clinical site monitoring services Serve as primary liaison between sponsor/Alimentiv and investigative sites to execute clinical Provide guidance and mentoring CRA I and II; collaborate with cross-functional stakeholders. Perform CRA Assessment Visits and participate in audits/inspections when required. 🎯 Requirements Minimum college diploma/degree with 4-6 years of related experience; health sciences, life Experience with Phase I–IV clinical trials; thorough knowledge of ICH-GCP and local regulatory Proficient in EDC systems (Medidata Rave, Oracle InForm), IRT, eTMF, CTMS, and Microsoft Office Ability to travel up to 40-60% depending on project assignment and site locations. Strong interpersonal, problem-solving, communication and organizational skills. 🎁 Benefits Home-based with regular travel. Sign-on bonus and annual incentives; additional stipends for communication costs and mobile phone
