As a Clinical Research Associate II you will work on the frontline of communication with project stakeholders ensuring timelines targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. You will focus on subjects rights safety and wellbeing and quality of data compliance.
Officebased role in Zagreb Croatia
Your responsibilities will include:
- Preparation conduct and reporting of all types of monitoring visits
- Supporting quality control such as compliance monitoring and reports review
- Contact for clinical investigators vendors and support services in regard to study progress
- Delivering training of investigators site staff and project teams
- Be involved in site identification process and feasibility research
- Support to Regulatory Affairs in procurement of site regulatory documents
- Preparation and delivering of presentations at Investigators Meetings
- Maintenance of studyspecific automated tracking systems
- Preparation for and attendance at companys audits; resolution of audit findings
Qualifications :
- Degree in Life Sciences (or similar) or an equivalent combination of education training & experience
- 1 year and a half of independent onsite monitoring experience in Croatia ideally on multiple projects at a time
- Experience in all types of monitoring visits in Phase II and/or III
- Native Croatian and full working proficiency in English
- Proficiency in MS Office applications
- Ability to plan multitask and work in a dynamic team environment
- Advanced communication collaboration and problemsolving skills
- As you will be monitoring multiple sites you must have a full and clean drivers license and the ability to travel.
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.
Remote Work :
No
Employment Type :
Fulltime