Clinical Research Associate

* Delivering training of investigators, site staff and project teams
* Work with complex studies
* Perform CRF review, source document verification and query resolution
* Be responsible for site communication and management
* Be involved in site identification process
* Contact for clinical investigators, vendors and support services in regard to study progress
* Participate in feasibility research
* Preparation and delivering of presentations at Investigator’s Meetings
* Preparation for and attendance at company’s audits; resolution of audit findings
* Support to Regulatory Affairs in procurement of site regulatory documents
* Maintenance of study-specific automated tracking systems

Qualifications
* College/University Degree in Life Sciences;
* At least 2 years experience in patient care and/or health care or clinical environment
* Full working proficiency in English
* Experience in Clinical Research is a plus
* Availability to travel
* Proficiency in MS Office applications
* Ability to plan and work in a dynamic team environment
* Communication, collaboration, and problem-solving skills

Additional Information
If you like to train and support others on their clinical research steps, and are also looking forward to future Lead Monitor roles, this position may just be the right one for you.
Advance your career in clinical research, coordinating a variety of tasks and learning new things while growing with a rapid growing company that puts its people first.

Company Description
We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 2,500 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.