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

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