Clinical Research Associate II

Hartmann Young is partnered with an ISO 9001–certified Contract Research Organisation (CRO) to appoint an experienced CRA II
. The company delivers high-quality clinical services across Non-Interventional studies, CTIMPs, ATMPs, rare disease and medical device trials, and is expanding due to internal growth and a strong study pipeline.

The CRA II will act as the primary contact for trial sites, ensuring high standards of compliance, documentation, and monitoring across multi-centre studies. You will support site teams and project teams to maintain trial quality and timelines.

• Conduct site selection, initiation, routine monitoring, and close-out activities
• Ensure compliance with GCP, ICH and regulatory requirements
• Build strong relationships with investigators, site staff, and clients
• Deliver SIV training and oversee CRF accuracy and SDV
• Prepare monitoring reports and escalate protocol deviations when required
• Support regulatory/ethics submissions and eTMF quality

• 2–3+ years’ clinical monitoring experience (CRA II or equivalent)
• Experience across Phases I–IV; life sciences degree. Strong focus on early phase.
• Strong knowledge of ICH-GCP; excellent communication and organisational skills