Job Description
📍UK, Remote (Must have UK Monitoring Exp)
Time Type: Full Time
Syneos Health is seeking a Single Sponsor Sr CRA with UK monitoring experience. This role involves site qualification, initiation, interim monitoring, site management, and close-out visits to ensure regulatory, ICH-GCP, and/or Good Pharmacoepidemiology Practice (GPP) compliance.
Responsibilities:
- Conduct site qualification, initiation, monitoring, and close-out activities both on-site and remotely.
- Verify informed consent, assess patient safety and data integrity, and ensure protocol adherence.
- Review source documents and CRFs, perform query resolution, and guide site staff.
- Manage investigational product (IP) handling including inventory, storage, dispensing, and compliance.
- Maintain and reconcile Investigator Site File (ISF) and Trial Master File (TMF).
- Document activities using letters, trip reports, logs, and tracking systems.
- Support patient recruitment, retention, and awareness strategies.
- Communicate site-level updates to project teams and adapt to changing priorities.
- Train and guide junior staff as needed and provide audit readiness support.
Qualifications:
- Bachelor’s degree or RN in a related field, or equivalent combination of education and experience.
- Knowledge of Good Clinical Practice/ICH Guidelines and applicable regulations.
- Strong computer skills and ability to adopt new technologies.
- Excellent communication, presentation, and interpersonal skills.
- Ability to manage travel up to 75% regularly.
To apply click the link below
Application Link:
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