Syneos Health is hiring an Unblinded CRA II/Senior CRA for a sponsor-dedicated role to ensure the highest quality of clinical research monitoring across our UK-based studies. You will be instrumental in safeguarding data integrity and participant safety through rigorous on-site and remote oversight.

What You'll Do

Conduct on-site and remote monitoring of clinical research studies to ensure compliance with widely accepted clinical practices and regulatory requirements.
Review study protocols, informed consent forms, and case report forms for accuracy and completeness.
Develop and implement tools, procedures, and processes to ensure quality monitoring.
Create monitoring plans, checklists, and templates to standardize study execution.
Contribute to the design, implementation, and delivery of processes, programs, and policies.
Participate in the development of standard operating procedures (SOPs) and training materials.
Manage defined components of projects or processes within your area of responsibility.
Coordinate site visits, track study progress, and resolve issues as they arise.
Ensure accurate and timely documentation of monitoring activities and findings.
Write monitoring reports, follow-up letters, and corrective action plans.
Collaborate with cross-functional teams to support efficient clinical trial operations.
Work closely with investigators, site staff, and other stakeholders to ensure smooth study conduct.

What We're Looking For

Bachelor's degree in a related field or equivalent practical experience.
Minimum of 2-4 years of experience in clinical research monitoring.
Strong knowledge of Good Clinical Practice (GCP) guidelines and relevant regulatory requirements.
Excellent written and verbal communication and interpersonal skills.
Ability to work independently and manage multiple priorities effectively.
Proficiency in using clinical trial management systems and other relevant software.
Attention to detail and strong analytical and critical thinking skills.
Proven problem-solving abilities.
Ability to work effectively in a team environment.
Strong organizational and time management skills.
Proficiency in the Microsoft Office Suite.

Nice to Have

Certified Clinical Research Associate (CCRA) or equivalent certification.

Technical Stack

Clinical trial management systems (CTMS)
Microsoft Office Suite

Team & Environment

At Syneos Health, we are passionate about developing our people through career progression. We are committed to our Total Self culture, where you can authentically be yourself. We are dedicated to taking care of our team and building a place where everyone feels they belong by bringing together a diversity of thoughts, backgrounds, cultures, and perspectives.