Senior Clinical Research Associate

United Kingdom

Full-Time, Part-Time

Immediately

With this application you apply directly to the company - without intermediaries, without detours.

Job Description

Upsilon Global are seeking a freelance CRA based in The UK to lead activities across UK for an upcoming psychedelics study of patients suffering from PTSD. The study is due to launch in January 2026, with some initial set-up/training activities scheduled for late November/December 2025.

The study will run for 3 years and study start-up, monitoring, site management and close-out activities are all expected. Dependant on the final number of confirmed sites and locations, this could be 0.8-1.0 FTE for 1 x CRA, or 0.4-0.5 FTE for 2 x CRAs.

Key information:

Position: Freelance CRA
FTE: 2 x 0.4-0.5 FTE or 1 x 1.0 FTE
Indication: Psychedelics for PTSD
Start Date: December 2025
Travel: Depending on site locations, either nationally or regionalised
Location: UK

Key Responsibilities:

Support with local submissions and site set-up activities
Conduct site visits, monitoring and assessment of clinical trial site, ensuring adherence to study protocols, Good Clinical Practice (GCP) guidelines, and applicable regulatory requirements.
Perform source document verification, data collection, and accurate recording of study data, ensuring data integrity and compliance.
Collaborate with site investigators, site staff, and study team members to ensure successful execution of clinical trials.
Assist in the development and review of study documents, including protocols, informed consent forms, and case report forms.
Maintain effective communication with study site, sponsors, and other stakeholders to provide timely updates, address queries, and resolve issues.
Monitor subject safety, reporting adverse events, and ensuring appropriate follow-up actions are taken.
Contribute to the preparation and coordination of study initiation, monitoring, and close-out activities.
Assist in the preparation and participation in regulatory inspections and audits as necessary.
Stay updated with current regulations, guidelines, and industry trends related to clinical research in translational/early-phase trials.

Experience:

5+ years independent monitoring experience
A strong background in psychedelic trial highly beneficial
Strong network of KOLs / PIs within the psychedelics and/or CBT area beneficial
In-depth knowledge of local regulatory requirements and clinical trial processes.
Strong organizational and communication skills, with the ability to manage multiple priorities.
Ability to work independently, demonstrating initiative, attention to detail, and problem-solving skills.

Job Requirements

Work permit in United Kingdom: Required

English language skill: Intermediate (B1)

Driver's license: Not required

Suitable Qualifications

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