ProPharma in the UK is seeking a Freelance Senior Clinical Research Associate to support monitoring across studies. You will conduct site visits, ensure adherence to protocol, SOPs, GCP, and applicable regulatory requirements, and contribute to site initiation, interim, and close-out activities.
This role requires 5+ years as a CRA, strong communication, EDC/CTMS/eTMF experience, and ability to work both in person and remotely within the UK and Ireland, with hybrid office-supported collaboration.
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Remote Freelance SCRA: Clinical Monitoring (UK & Ireland) employer: ProPharma
ProPharma is an exceptional employer that fosters a culture of diversity, equity, and inclusion, empowering employees to be their authentic selves while driving innovation in the healthcare sector. With a commitment to employee growth, ProPharma offers opportunities for professional development and collaboration, particularly in its Eastern European hubs, where remote work is supported alongside hybrid office engagement. Join us to make a meaningful impact in the field of compliance and quality assurance, all while enjoying a supportive and dynamic work environment.
