Single Sponsor Senior CRA II (Site Care Partner II) UK based only.

About This Opportunity

Our talent team is representing a confidential life sciences organization seeking a Senior Clinical Research Associate for their UK-based operations. This single-sponsor role focuses on site monitoring and management across the clinical trial lifecycle. You will work remotely within the United Kingdom, with regular travel to investigator sites (up to 75%).

We are looking for an experienced CRA who can operate independently, mentor junior staff, and ensure regulatory compliance while maintaining strong relationships with site personnel.

Responsibilities

• Conduct site qualification, initiation, monitoring, and close-out visits (on-site and remotely) ensuring ICH-GCP, regulatory, and protocol compliance
• Perform source document verification and reconcile clinical data entered in case report forms against medical records and site documentation
• Verify informed consent processes and documentation; maintain subject confidentiality and assess factors affecting patient safety and data integrity
• Monitor investigational product accountability, storage, dispensing, and administration per protocol requirements
• Review Investigator Site Files for accuracy and completeness; ensure proper archiving of essential documents per local regulations
• Document monitoring activities through trip reports, follow-up letters, communication logs, and tracking systems
• Manage site-level communication and activities to meet project timelines and deliverables; adapt quickly to changing priorities
• Support subject recruitment and retention strategies; escalate serious issues and develop action plans as needed
• Provide training, mentorship, and supervision to junior CRA staff; perform sign-off visits for less experienced team members
• Prepare for and participate in investigator meetings, clinical monitoring meetings, and training sessions
• Support audit readiness standards at site and project levels; assist with audit preparation and follow-up actions
• For real-world late phase studies: conduct chart abstraction, collaborate with medical science liaisons, identify sites based on local treatment patterns, and contribute to regulatory documentation

What We're Looking For

• Education: Bachelor's degree or Registered Nurse qualification in a related field, or equivalent combination of education, training, and experience
• Regulatory Knowledge: Strong understanding of Good Clinical Practice/ICH Guidelines and applicable regulatory requirements
• Technical Skills: Proficiency with clinical trial software, electronic data capture systems, and general computer applications; ability to embrace new technologies
• Communication: Excellent written and verbal communication skills, presentation abilities, and interpersonal effectiveness
• Critical Thinking: Moderate to advanced problem-solving skills with ability to evaluate site performance and provide strategic recommendations
• Travel: Ability and willingness to travel up to 75% within the UK on a regular basis
• Location: Must be based in the United Kingdom; this role is UK-only
• Experience: Senior-level CRA experience with demonstrated ability to work independently and mentor others

How We Work With You

When you apply through Get A Job.ai, our recruiting team will review your background and conduct an initial screening conversation. If there's a strong match, we'll prepare and submit your profile to our client for consideration. Please do not contact the employer directly—all communication regarding this opportunity should go through our team to ensure the best outcome for your candidacy.

Pay

Compensation details will be discussed during the screening process based on your experience and qualifications.

Equal Opportunity: Get A Job.ai is committed to inclusive hiring practices. We welcome applications from candidates of all backgrounds and provide equal employment opportunities regardless of race, color, religion, sex, national origin, age, disability, or any other protected characteristic.