Senior Clinical Research Associate III

Caidya; London; Remote; GBP 100,000 - 125,000; Full time

Job summary

A growing clinical research organization is seeking a Senior Clinical Research Associate III to lead monitoring efforts across clinical trials. This remote role involves ensuring compliance with protocols, liaising with investigational sites, and mentoring junior colleagues. Candidates should have significant clinical monitoring experience and preferably a degree in healthcare or life science. Join us to impact future clinical trials effectively.

Qualifications

• Experience in on-site monitoring of clinical studies.
• Experience with various clinical study types including inpatient and Phase I.
• Ability to travel up to 80%.

Responsibilities

• Act as the primary liaison between Sponsor and investigational sites.
• Conduct all types of site visits per monitoring plans.
• Verify subject eligibility and informed consent.

Skills

Effective negotiation

Conflict resolution

Data collection accuracy

Education

4-year college degree in healthcare or life sciences

5+ years of relevant clinical research experience

Job description

Job Title

Senior Clinical Research Associate III

Job Location: London, UK - home based (any UK location considered)

Ready to take the lead in cutting-edge clinical research? Caidya is looking for an experienced Senior Clinical Research Associate III to join our small, collaborative team in the UK. This is your chance to make an impact in a growing CRO, driving the future of clinical trials across oncology studies.

Why Join Us?

At Caidya, we do more than run clinical trials — we build partnerships that transform lives. You’ll be at the heart of high-quality data, patient safety, and innovation in global research. We value your independence, your expertise, and your drive to lead.

Job Overview

The Senior Clinical Research Associate III monitors investigational sites to ensure subject safety and provide high quality data review and reporting in compliance with the Caidya and/or client Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/International Conference on Harmonization (ICH) guidelines, ISO14155, and other applicable regulations. Builds, manages and supports strong site relationships while serving as liaison between the Sponsor and assigned sites.

Job Duties and Responsibilities

• Act as the primary liaison between Sponsor and investigational sites.
• Conduct all types of site visits (pre-study, initiation, interim, and close-out) per monitoring plans.
• Ensure compliance with protocols, GCP/ICH guidelines, SOPs, and applicable regulations.
• Verify subject eligibility, informed consent, safety, and accurate data collection.
• Perform source data verification and ensure timely resolution of queries.
• Manage investigational product accountability and trial supplies.
• Support site start-up, regulatory document collection, and IRB/IEC submissions.
• Identify, escalate, and resolve site issues proactively.
• Participate in audit preparation, training, feasibility assessments, and team meetings.
• Provide mentorship to CRAs and contribute to project training and documentation.
• Assist with sponsor communication, protocol clarifications, and budget coordination.
• May support bid defense presentations and co-monitoring activities.

Supervisory Responsibilities

No supervisory responsibilities.

Job Requirements

• Education
  • 4-year college graduate, preferably with a healthcare or life science degree.
  • In lieu of a degree, candidates with 5 or more years of relevant clinical research experience in pharmaceutical or CRO industries will be considered.
• Experience
  • Significant experience in on-site monitoring of clinical studies.
  • Monitoring experience in multiple, complex indications and study types including inpatient, FIH, Phase I, critical care.
  • Experience in all areas of monitoring (on-site, remote, etc.)
• Capabilities
  • Ability to negotiate effectively, resolve conflicts and build consensus.
  • Ability to drive an automobile and have a valid driver’s license, if applicable.
  • Valid passport required in the case of international business travel.
  • Ability to travel up to 80%.

If you're a motivated CRA ready to make a difference in a company that values your voice — we want to hear from you.

Apply now and help shape the future of clinical trials at Caidya.

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The company will not accept unsolicited resumes from third party vendors.