Precision for Medicine, Oncology and Rare Disease is looking for a Senior Clinical Research Associate to manage and perform monitoring visits in sites in Portugal, ensuring that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards.
Requirements
- 3+ years of CRA experience within the CRO or pharmaceutical industry
- experience in managing the sites in Portugal
- start up activities experience
- fluency in Spanish, Portuguese and English
- understanding of financial management (preferred)
- graduate or postgraduate degree with a concentration in a scientific or healthcare discipline (preferred)
Responsibilities
- monitor and own the progress of clinical studies at investigative sites
- ensure that clinical studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and all applicable regulations and standards
- coordinate all necessary activities required to set up and monitor a study
- identify potential study risks and propose solutions on how to mitigate them
- handle appropriately sized clinical trials, and support Project Managers with trials that are larger in scope
- train and mentor junior staff members
- interact directly with clients, initiate payments, and participate in proposal activities, including development and client presentations
Other
- 4-year college degree or equivalent experience
- availability for domestic travel including overnight stays, which may constitute up to approximately 50-60% travel commitment
- location: Spain - Madrid or Barcelona
- calm, thoughtful, and responsive when things don’t go as planned
- well-prepared, whether it be for an investigator meeting, site visit or project team update, always staying two steps ahead of the game
