Remote SCRA: Senior Clinical Research Associate(UK/Ireland)

ProPharma; Dublin; Remote; EUR 85,000 - 120,000; Part time

Job summary

ProPharma is seeking a Freelance Senior Clinical Research Associate to support UK & Ireland studies. The role covers in-person and remote monitoring across assigned sites, ensuring adherence to protocol, SOPs, GCP, and regulatory requirements.

Responsibilities include monitoring visits, report writing, site initiation, and collaboration with investigators and project teams. A Bachelor’s degree and 5+ years CRA experience are required for this remote, international opportunity.

Qualifications

• Bachelor’s degree or equivalent combination of education and experience.
• “5+ years” of experience as a Clinical Research Associate.
• Experience working in regulated environments and GCP compliance.

Responsibilities

• Monitor assigned clinical sites per protocol and SOPs.
• Prepare monitoring reports within SOP/regulatory timelines.
• Assist with site initiation, interim and closeout visits.
• Oversee regulatory document accuracy and site communications.
• Coordinate with sites, investigators and cross-functional teams.
• Support study start-up activities when needed.
• Maintain high-quality data and source documentation review.

Skills

Communication skills

Proficient in MS Office

EDC/CTMS/IVRS/eTMF

Regulatory knowledge (ICH/GCP)

Prioritization & planning

Attention to detail

Cross-functional collaboration

Education

Bachelor's degree or equivalent

Tools

EDC

CTMS

IVRS

eTMF

Job description

ProPharma is seeking a Freelance Senior Clinical Research Associate to support UK & Ireland studies. The role covers in-person and remote monitoring across assigned sites, ensuring adherence to protocol, SOPs, GCP, and regulatory requirements.

Responsibilities include monitoring visits, report writing, site initiation, and collaboration with investigators and project teams. A Bachelor’s degree and 5+ years CRA experience are required for this remote, international opportunity.