Experienced Clinical Research Associate - Sponsor Dedicated - Cz Republic
IQVIA
Czech Republic
Not specified; not specified; compyny car, mobile ...
Good clinical practice compliance
International conference on harmonization guidelines
Czech and english language fluency
The role involves performing site selection, initiation, monitoring, and close-out visits for clinical trials
Job Summary
The role involves performing site selection, initiation, monitoring, and close-out visits for clinical trials.
Candidates must evaluate the quality and integrity of site practices in accordance with regulatory requirements like GCP and ICH guidelines.
The company offers a stable international environment with resources for career growth, flexible schedules, and a benefits package including a company car.
Matching Summary
The role involves performing site selection, initiation, monitoring, and close-out visits for clinical trials.
Salary
Not specified; Not specified; Company car, mobile phone and attractive benefits package
Skills & Requirements
Must-have
Good Clinical Practice compliance
International Conference on Harmonization guidelines
Czech and English language fluency
MS Office computer skills
Site selection and initiation visits
Nice-to-have
Flexible work schedule support
Therapeutic knowledge development
Effective client relationship building
Strong problem-solving abilities
Organizational time management skills
Key Requirements
University degree in scientific discipline or health care
At least 2 years of experience as a Clinical Research Associate