Clinical Research Associate - Multi-Sponsored Model
QHR IQVIA Zagreb d.o.o.
Apply to this jobIf you are looking to upgrade your CRA career, this is your chance to connect with us and explore opportunities within a leading global CRO!
While projects vary, your typical CRA responsibilities will include
- Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
- Supporting the development of a subject recruitment plan
- Establishing regular lines of communication plus administering protocol and related study training to assigned sites
- Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
- Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
You should have
- A Bachelor's degree in a health care, MD or Pharmacist preferred.
- At least 1 year of on-site monitoring experience.
- Good written and verbal communication skills including fluent command of English and Serbian language.
- A valid driver´s license as the role requires frequent travel to sites.
- You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. You also have a good knowledge of applicable clinical research regulatory requirements.
Apply now and let´s connect for current and/or future opportunities!
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.
Summary
Monitor clinical sites, support protocol adherence, and ensure data integrity in clinical research.
Job title
Clinical Research Associate - Multi-Sponsored Model
Experience level
1+ years
Minimum experience
1+ years exp
Industry
healthcare
Location requirements
Belgrade, Serbia; remote work not specified.
Salary
Not specified
Management role
No
Required skills
Preferred skills
Specializations
Structured locations inferred from the posting.
Belgrade, Serbia