Clinical Research Associate II – Senior Clinical Research Associate

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

📋 Description

• Oversee and take ownership of the progress of clinical studies at investigative sites.

• Ensure that clinical studies are performed, documented, and reported in accordance with the protocol, SOPs, ICH-GCP, and relevant regulations and standards.

• Coordinate the necessary activities to establish and monitor studies.

• Identify and engage investigators.

• Assist in the preparation of regulatory submissions.

• Conduct pre-study evaluations and initiation visits.

• Recognize potential risks associated with studies and suggest mitigation strategies.

• Prepare for investigator meetings, site visits, and updates for the project team.

• Manage conflicts by employing effective resolution strategies.

• Assume responsibility for the quality and results of work delivered.

⛳️ Requirements

• A 4-year college degree or equivalent experience.

• Over 1 year of Clinical Research Associate (CRA) experience in a CRO or pharmaceutical environment is preferred.

• Experience in oncology is essential.

• Experience in Phase I studies is desirable, but not mandatory.

• First-In-Human (FIH) experience is also desirable, though not essential.

• Willingness to travel domestically, including overnight stays, with a commitment of approximately 50–60% travel.

• Some senior-level positions may require international travel.

• Proficiency in English is required.

• Must have legal authorization to work in the country of employment without the need for employer sponsorship.

🏝️ Benefits

• A lower than average number of protocols.

• Reasonable travel requirements and an improved work/life balance.

• Direct support from line management.

• Opportunities to contribute ideas and have them valued and developed.

• A fully home-based working arrangement.