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 trials at investigative sites.

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

• Coordinate the necessary activities to establish and monitor studies.

• Identify suitable investigators for the studies.

• Assist in the preparation of regulatory submissions.

• Conduct pre-study and initiation visits.

• Participate in investigator meetings, site visits, and project team updates.

• Recognize potential study risks and suggest mitigation strategies.

• Manage conflicts utilizing resolution techniques.

• Facilitate the execution of targeted, adaptive clinical trials in oncology and rare diseases.

⛳️ Requirements

• A bachelor's degree or equivalent professional experience.

• Over 1 year of Clinical Research Associate (CRA) experience within the Clinical Research Organization (CRO) or pharmaceutical sector (preferably).

• Experience in oncology is essential.

• Phase I experience is advantageous, though not mandatory.

• First-In-Human (FIH) experience is a plus, though not required.

• Willingness to travel domestically, including overnight stays, approximately 50–60% of the time.

• Proficiency in English.

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

🏝️ Benefits

• Exceptional CRA retention rates and a supportive work culture.

• Fewer protocols compared to the industry average.

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

• Direct line management support.

• Opportunities to have influence and make an impact in a smaller CRO.

• Support for professional growth.

• Fully remote work arrangement.