Clinical Research Associate

ProPharma is a leading provider of clinical research solutions. We empower biotech, med device, and pharmaceutical organizations to advance scientific breakthroughs and introduce new therapies.

We are seeking an experienced Clinical Research Associate (CRA) with expertise in pulmonary and cardiovascular trials to join our team in Croatia.

As a CRA, your work will directly contribute to improving lives globally. You'll collaborate with top-tier professionals, work on impactful studies, and grow your expertise within a supportive culture.

• Conduct monitoring visits at study sites, ensuring compliance with GCP, SOPs, and study protocols.

• Support start-up activities, including site identification, feasibility assessments, document collection, and regulatory submissions.

• Train and support site staff on protocol adherence, source documentation, and CRF completion.

• Review source documents and CRFs for accuracy, completeness, and data integrity.

• Manage investigational product supplies and reconcile inventory at sites.

• Ensure timely reporting of protocol deviations, SAEs, and other key study metrics.

• Maintain communication with investigators, site staff, sponsors, and cross-functional teams.

• Participate in internal and sponsor meetings as needed.

• Bachelor's degree in life sciences or related field.

• Minimum 3 years of CRA experience with demonstrable knowledge in therapeutic areas, including pulmonary and cardiovascular trials.

• Strong knowledge of ICH-GCP, local regulatory requirements, and international clinical research standards.

• Proficient with EDC, CTMS, IVRS, and eTMF systems.

We celebrate diversity and strive to create a workplace where each person can thrive. We provide opportunities for growth, collaboration, and professional development.

Join us in shaping the future of clinical research