Sr. Clinical Research Associate (Poland)

📋 Description

• Independently perform and oversee site monitoring activities (onsite and remote).
• Collaborate with site staff to ensure data accuracy and regulatory compliance.
• Monitor data queries and coordinate resolution; ship clinical supplies as needed.
• Ensure site staff are trained on protocol, plans, systems, and ICH-GCP.
• Participate in study progress meetings and document review (ISF/TMF).
• Act as primary site contact and oversee overall study integrity and training.

🎯 Requirements

• College diploma/degree with 4-6 years of related experience.
• Strong communication, attention to detail, and problem-solving abilities.
• Ability to travel 40-60% depending on project/location.
• Health Sciences, Life Sciences, Pharmacy, or Nursing degree preferred; or Sr.CRA/ACRP certification.
• Experience in Phase I–IV trials; thorough knowledge of ICH-GCP and local rules.
• Proficient in EDC systems (Medidata Rave, Oracle InForm), IRT, eTMF, CTMS, and MS Office.

🎁 Benefits

• Home-based role with regular travel expectations.