Note: The job is a remote job and is open to candidates in USA. i-Pharm Consulting is seeking a Contract Clinical Research Associate to support oncology studies for a large global CRO client. The role involves regional site monitoring, ensuring compliance and data integrity throughout the trial process.
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
- Supporting enrolment performance and study timelines
Skills
- 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
- Supporting enrolment performance and study timelines
- Phase I experience
- Prior exposure to lung or bladder cancer studies
Benefits
- Home-based
- Exposure to complex Phase I oncology trials
Company Overview