Senior CRA
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About the role
Full-time Senior CRA role based in Skopje, North Macedonia, supporting Phase II and/or III clinical studies. Responsibilities include independent on-site monitoring, site management, data and query review, regulatory submission support, feasibility work, and audit or inspection preparation. A Life Sciences degree or equivalent education, training and experience, monitoring experience, English and Macedonian proficiency, travel availability, and a valid driver’s license are required.
Key requirements
- • College/University degree in Life Sciences or an equivalent combination of education, training & experience
- • Required skills: Independent on-site monitoring, SIV, RMV and COV monitoring visits, CRF review, Source document verification, Query resolution, Site communication and management, Vendor and in-house support coordination, Study progress communication, Feasibility research, Regulatory submission support, Audit and inspection preparation, Ability to travel, Planning and multitasking, MS Office applications, Communication, collaboration and problem-solving
- • Required languages: English, Macedonian
- • Professional registration/licence (North Macedonia)
Opportunity details
- • Workplace: On Site
- • Employment: Permanent
- • Posted: Jul 29, 2026
- • Original advert language: English
Full vacancy
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Employer’s role description
Job title: Senior CRA
Location: Skopje, SK, North Macedonia
Employment type: Full-time
Company Description
We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global, mid-size company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.
Job Description
We are looking for an experienced Senior CRA to support us with the following responsibilities in North Macedonia:
- Conduct and report SIV, RMV, COV onsite monitoring visits
- Perform CRF review, source document verification and query resolution
- Be responsible for site communication and management
- Be a point of contact for in-house support services and vendors
- Communicate with internal project teams regarding study progress
- Participate in feasibility research
- Support regulatory team in preparing documents for study submissions
- Prepare and participate in audits and inspections
Qualifications
- College/University degree in Life Sciences or an equivalent combination of education, training & experience
- Independent on-site monitoring experience
- Experience in all types of monitoring visits in Phase II and/or III
- Full working proficiency in English and Macedonian is essential.
- Proficiency in MS Office applications
- Ability to plan, multitask and work in a dynamic team environment
- Excellent communication, collaboration, and problem-solving skills
- Ability to travel
- Valid driver’s license
Additional Information
This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.
Verification
- ✓ Employer verification
- ✓ Original posting located
- Last verified: Sep 24, 2026