Clinical Research Associate
Your responsibilities will include:
- Performing site selection, initiation, monitoring and close-out visits
- Supporting the development of a subject recruitment plan
- Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines
- Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions
- Collaborating with experts at study sites and with client representatives
Qualifications:
- University degree in scientific discipline or health care
- At least 2 year of experience as a Clinical Research Associate.
- Very good computer skills including MS Office
- Excellent command of Czech and English language. CZ Republic based.
- Organizational, time management and problem-solving skills
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
- Flexibility to travel
- Driver’s license class B
What you can expect:
- Resources that promote your career growth
- Leaders that support flexible work schedules
- Programs to help you build your therapeutic knowledge
- Excellent working environment in a stabile, international, reputable company
- Company car, mobile phone and attractive benefits package
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
Seen 26 days ago.
Original posting on IQVIA's site ↗
Posting text belongs to the employer. Removal requests: contact us.
Nearby
Live postings like this one
Same employer first, then the same role elsewhere.
- 9h ago
- 9h ago
- 9h ago
- 9h ago
- 9h ago
Associate Clinical Trial Management Director (ACTMD)
Parsippany New Jersey United States of America
9h agoAssociate Clinical Trial Management Director (ACTMD)
Durham North Carolina United States of America
9h ago- 9h ago
One job at a time
One posting. One CV. $25.
Pick the job you actually want and we write for it.