Note: The job is a remote job and is open to candidates in USA. i-Pharm Consulting is seeking Clinical Research Associates to join their Full Service clinical operations team, supporting global studies across various therapeutic areas. This home-based role involves regional site monitoring, ensuring compliance, patient safety, and collaboration with study teams and investigators.
Responsibilities
- Conducting on-site and remote monitoring visits across assigned investigative sites
- Ensuring compliance with ICH-GCP, protocol requirements, and regulatory standards
- Supporting site activation, maintenance, and close-out activities
- Verifying source data, resolving queries, and ensuring data integrity
- Building strong relationships with investigators and site staff
- Contributing to study timelines, enrolment performance, and overall study quality
Skills
- Experience in monitoring within a CRO or pharmaceutical environment is required, ideally with exposure to multi-site, late-phase studies
- Prior monitoring experience required in one of these areas: Cardiovascular, CNS (Central Nervous System), Diabetes, GLP-1 / Metabolic Disease
- CRA II (1–3 years' experience) or Senior CRA I (3–4 years' experience)
- Ensuring compliance with ICH-GCP, protocol requirements, and regulatory standards
- Conducting on-site and remote monitoring visits across assigned investigative sites
- Supporting site activation, maintenance, and close-out activities
- Verifying source data, resolving queries, and ensuring data integrity
- Building strong relationships with investigators and site staff
- Contributing to study timelines, enrolment performance, and overall study quality
Benefits
- Fully remote role (US-based, home-based flexibility)
- Strong pipeline of global clinical studies
- Opportunity to work across high-growth therapeutic areas
- Exposure to full-service clinical trial delivery
- Clear progression within clinical operations
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