Meeveem Limited is recruiting a Senior Clinical Research Associate to lead site qualification, initiation, monitoring, and close-out visits, ensuring GCP compliance. You will validate source documents, monitor data integrity, and manage IP and TMF correspondence, with on-site or remote evaluations.
The role requires strong communication, regulatory knowledge, and willingness to travel up to 75% domestically and internationally as needed. Prior CRO/PHARM experience is expected.
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Clinical Research Monitor & Site Management employer: Meeveem Limited
Meeveem Limited is an excellent employer for general practitioners, offering a supportive and flexible work environment that prioritises professional growth and work-life balance. With full indemnity cover, NHS Pension, and generous leave, our team members enjoy a culture of collaboration and continuous development across our two sites, making it an ideal place for those seeking meaningful and rewarding employment.
