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.