This is a fully remote position, open to applicants in United Kingdom.

📋 Description

• You will oversee and manage the progression of clinical studies at investigative sites, ensuring that these studies are conducted, documented, and reported in accordance with the protocol, SOPs, ICH-GCP, and all relevant regulations and standards.

• You will facilitate all essential activities necessary for setting up and monitoring a study, which includes identifying investigators, assisting with regulatory submissions, and conducting pre-study and initiation visits, among other tasks.

⛳️ Requirements

• A bachelor's degree or equivalent experience is required.

• Ideal candidates should possess over 1 year of experience as a Clinical Research Associate (CRA) within the CRO or pharmaceutical sector.

• Experience in oncology and early-phase studies is preferred, though not mandatory.

• Willingness to travel domestically, including overnight stays, which may require a travel commitment of approximately 50-60% (some senior-level positions may involve international travel).

• Proficiency in English is essential.