Adverse Event Jobs

Join Intuitive as a Post Market Surveillance Adverse Event Analyst to investigate serious device-related complaints, make regulatory reporting decisions, and drive complaint lifecycle closure for a market-leading medical device company.

Experienced Clinical Research Coordinator needed to lead and coordinate vaccine trial activities onsite at a Profound Research community site in Oceanside, CA.

Care Access is hiring a Travel Clinical Research Coordinator in Raleigh, NC to manage decentralized clinical trial activities nationwide, ensuring protocol and regulatory compliance while supporting sites and study participants.

AssistRx is hiring a licensed Florida pharmacist to oversee prescription dispensing, supervise pharmacy technicians, and provide clinical oversight in a closed-door specialty/mail pharmacy operating weekdays.

Support patient safety and care continuity as an Outbound Contacts Representative 2 at CenterWell by managing ADE reporting, clinician outreach, and patient communications.

The University of Kansas Cancer Center is hiring a Clinical Research Coordinator to coordinate and monitor oncology clinical trials, manage data and regulatory documentation, and support patient-facing research activities.

Eurofins is hiring a remote Pharmacovigilance Specialist (DVM) to drive post‑marketing safety surveillance, signal detection, and provide PV expertise across product lines.

Care Access is hiring a Travel Clinical Research Coordinator based in Mobile, AL to manage and monitor decentralized clinical trials nationwide with high travel requirements and strong adherence to GCP and regulatory standards.