Site Care Partner

About the role

The Site Care Partner supports clinical studies by overseeing site activities from qualification through close‑out, ensuring regulatory compliance and data quality while protecting patient safety and confidentiality.

Key responsibilities

• Perform site qualification, initiation, interim monitoring, management and close‑out visits (on‑site or remotely) ensuring compliance with regulatory, ICH‑GCP and protocol requirements.
• Evaluate overall site performance, provide recommendations, and promptly communicate or escalate serious issues to the project team.
• Maintain up‑to‑date knowledge of ICH/GCP guidelines, relevant regulations and company SOPs.
• Verify that informed consent is obtained and documented correctly for each subject/patient.
• Protect subject/patient confidentiality and assess factors affecting safety and data integrity, including protocol deviations and pharmacovigilance issues.
• Conduct source document reviews, verify that clinical data entered in case report forms (CRFs) are accurate and complete.

Required profile

• Experience in clinical site monitoring or site management within a biopharmaceutical environment.
• Strong understanding of ICH‑GCP, Good Pharmacoepidemiology Practices and applicable regulatory guidance.
• Ability to use professional judgment to assess site processes and develop action plans.
• Excellent communication skills for reporting and escalating issues.
• Commitment to maintaining patient confidentiality and data integrity.

Required skills

• Clinical monitoring
• Regulatory compliance (ICH/GCP)
• Source document review
• Case report form (CRF) verification

What we offer

• Career development and progression opportunities.
• Supportive line management and peer recognition.
• Total rewards program and a culture that encourages authenticity.