Clinical Research Associate II (CRA II)

Clinical Research Associate II focuses on delivering study-specific training at site initiation visits (sivs).

What the role involves

• Delivering study-specific training at Site Initiation Visits (SIVs).
• Managing case report form (CRF) data accuracy and source data verification (SDV).
• Preparing visit reports, follow-up letters, and monitoring documentation.
• Collaborate with eTMF specialists, CRAs, and project managers to maintain trial quality.
• 2–3+ years’ CRA experience (at CRA I or II) monitoring multi-centre clinical trials preferably early phase.
• Degree in a life sciences or related field.

Skills and requirements

• Familiarity with ISO 14155 and medical device regulations.

Confirmed role details

• Role Type: Remote.
• Competitive salary + car allowance & benefits.
• Start Date: July-September 2026.
• As an ISO 9001 certified, organisation PHARMExcel prides itself in delivering high quality and results driven clinical services.

Candidate fit

• clinical judgement, NMC standards, calm communication, and careful documentation

Additional role context

• Excellent report writing and compliance with timelines will be expected.
• Build strong relationships with our clients, investigators, and site teams.
• Ensure compliance with GCP, ICH, ISO 14155, and regulatory standards.