Sr. Clinical Research Associate
New
Belgrade, SerbiaFull-TimeSenior
Salary not disclosed
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Job Details
- Experience
- 4-6 years
- Required Skills
- GCP
Requirements
- Minimum of a college diploma or degree.
- 4-6 years of related clinical research experience.
- Strong understanding of GCP (Good Clinical Practice) best practices.
- Experience with regulatory filings and site budget monitoring.
- Ability to act as a subject matter expert and provide mentorship to peers.
- Demonstrated critical thinking and problem-solving abilities.
- Strong communication skills and attention to detail.
- Ability to regularly travel to sites, including in Bosnia and Croatia.
- Self-motivated with a commitment to achieving results.
Responsibilities
- Manage and deliver full clinical site monitoring services for complex or multinational projects.
- Act as Lead CRA to direct project activities, review reports, and serve as the primary liaison between CRAs and project teams.
- Identify and recruit site investigators and coordinate the delivery of trial materials, samples, and documentation.
- Provide mentorship, training, and performance feedback to peer CRAs and assist with supervision tasks.
- Ensure site compliance with SOPs, study guidelines, and GCP best practices throughout the project lifecycle.
- Facilitate resolution of site and patient issues, serving as the first point of escalation.
- Collaborate with project teams to provide ongoing updates and feedback to investigational sites.
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