Clinical Research Associate
PSI CRO · Trebinje
Job description
About the role
As a Clinical Research Associate at PSI CRO you will conduct monitoring activities across various therapeutic indications, ensuring the highest quality standards in clinical research.
Key responsibilities
- Conduct and report all types of onsite monitoring visits.
- Participate in study startup, perform CRF review, source document verification and query resolution.
- Manage site communication, act as point of contact for internal support services and vendors.
- Support regulatory team with document preparation for study submissions and assist in audits and inspections.
Required profile
- College/University degree in Life Sciences or equivalent.
- At least 1 year of independent on‑site monitoring experience.
- Full working proficiency in English and Serbian.
- Valid driver’s license and ability to travel across the region.
Required skills
- Proficiency in MS Office applications.
What we offer
- Permanent full‑time contract with stability and long‑term cooperation.
- Remote work setting, car allowance, laptop and mobile phone.
- Career development through onboarding courses, mentoring and on‑the‑job training.
- Supportive colleagues and comfortable office in Banja Luka.
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Published 4 hours ago
Expires 1 month from now
2 views · 0 interested
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PSI CRO
Trebinje