STUDY COORDINATOR

at  KCR Placement

KCR Placement is a full-service functional sourcing and recruitment provider. We specialize in high-speed and high-quality talent sourcing for the CRO, Pharmaceutical, Biotech and Medical Device industries across Europe.
Our employees are KCR Placement’s most crucial asset. We commit to placing our candidates at the center of all we do and prepare them for long-term career development and success with competitive benefits and vibrant work environment.
The KCR Placement team is supported by a specialized referral network of expert professionals and is dedicated to providing sourcing services and client support from job requisition to job offer.
We are currently seeking highly motivated individuals to serve as Clinical Study Coordinators

DESIRED SKILLS AND EXPERIENCE:

• At least 1 year of experience;
• University degree in medicine, biotechnology, pharmacy, nursing or biology;
• Knowledge of English;
• Very good understanding of ICH-GCP guidelines, previous; experience in clinical trials would be a strong asset;
• Availability to work at the clinical research site;
• Strong organizational, communication and teamwork skills;
• Computer literacy;
• Mobility;
• Time flexibility.

• Supervision over the completeness of the Study documentation;
• Supplementing and updating of the Study’s documentation; (including patients’ ICFs, sending/receiving Study’s documentation, obtaining certificates, CVs and documents confirming the completion of trainings);
• Cooperation with external suppliers (central laboratory, couriers, etc.);
• Sending materials for assessment, access to webpages of service providers in the Study;
• Coordination of the Center’s work as part of the Study and unification of communication with the Sponsor or CRO on behalf of the Investigating Team, with Investigator, hospital’s pharmacy, laboratory, etc;
• First contact for the CRA;
• Support for CRA during monitoring visits, closing and opening visits in the Centre (including arranging of the visits, preparation of documentation for verification, confirmation of the Investigator’s availability, organization of a visit to a pharmacy, laboratory, etc.), participation in audits (if required), day-to-day administrative activities connected with the completion of databases (eCRF), orders within the frame of the Study;
• Arranging Patient visits (including reminding Patients about the visits);
• Active screening for potential Patients according to Investigator’s instructions;
• Other activities directly related with the Study as instructed by the Investigator, provided that Coordinator has no right to provide medical services to the Patients.