CRA I/II or Senior CRA

Proclinical Group; Remote; GBP 60,000 - 80,000; Full time

Job summary

A leading life sciences recruitment agency is looking for Clinical Research Associates to conduct clinical trials remotely in the chronic disease area. This role involves site visits, monitoring activities, and maintaining communication with study teams. Candidates should have clinical research experience and strong organizational skills. This position offers the opportunity for meaningful contributions to research and long-term career growth.

Qualifications

• Experience in Clinical research, preferably within a CRO or pharmaceutical setting.
• Previous history of independent monitoring experience is required.
• Background in diabetes or obesity therapeutic areas is beneficial.

Responsibilities

• Conduct site visits within the select region.
• Perform monitoring activities to ensure adherence to compliance standards.
• Work closely with site staff to ensure proper documentation and data collection.
• Support study start‑up, maintenance, and close‑out activities.
• Provide updates and reports on site performance and study progress.

Skills

Clinical research experience

Independent monitoring experience

Strong organizational skills

Strong communication skills

Capacity to travel

Job description

Are you a dedicated individual looking to put your expertise to work fully flexibly in a remote position? We are on the hunt for experienced CRAs and you could be a perfect fit!

Proclinical is seeking two Clinical Research Associates to join our client on a remote working basis. This position will be responsible for conducting clinical trials in the chronic disease field and provides an exciting opportunity to contribute to meaningful research with strong long-term career growth potential.

Responsibilities:

• Conduct site visits within the select region.
• Perform monitoring activities to ensure adherence to compliance standards with study protocols, regulatory requirements, and GCP.
• Work closely with site staff to ensure proper documentation and data collection.
• Support study start‑up, maintenance, and close‑out activities.
• Maintain effective communication with study teams and stakeholders.
• Provide updates and reports on site performance and study progress.

Key Skills and Requirements:

• Experience in Clinical research, preferably within a CRO or pharmaceutical setting.
• Previous history of independent monitoring experience is required.
• Background in diabetes or obesity therapeutic areas is beneficial but not essential.
• Strong organizational and communication skills.
• Capacity to travel regionally as the business requires.
• Academic candidates with relevant experience, including monitoring, will also be considered.

If you are having difficulty in applying or if you have any questions, please contact Erin Magalie at [e-mail].

Apply Now:

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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