CORE JOB TASK

* Lead CRC team.and supervise of the implementing and conducting clinical studies on site by CRC in accordance with applicable regulatio, GCP/ICH guidelines, and applicable SOPs.

* Generate clinical project plan including timeline projection and operation on site strategy.

* Design related associated Forms and CRC workbook

* Prepare and implement project-specific training programs and presentatio for internal and external clinical team,

* Participate in and provide support investigator meetings, including presentatio.

* Participate in CRC on site at fit time

* Be overall respoible for protocol compliance across all sites, and on-time study milestone delivery

* Provide regular co-operation on site and project status reports for both internal and external clients as agreed.

* Review CRC regular reports and correspondence. Make recommendatio regarding monitoring, safety, eligibility, enrolment, and data coistency, and be involved in issue escalation and resolution.

* Track and eure study budget according to the agreement.

* Mentor and coach CRCs and project manage (senior PM only).

* Provide input to study proposal and budgets as needed.

MINIMUM REQUIREMENTS

* A Bachelor Degree in a medical, health, or science related are, or a nuing degree.

* Minimum of 3 yea related experience in clinical research and project management.

* Thorough undetanding of all relevant ICH-GCP guidelines and regulatio.

* Good verbal and written communication skills.

* Good team player, self-motivated and attention to details.

* Demotrated leadehip, influence and problem-solving skills.

* Strong customer focused seitivity towards internal and external custome.

* Must be able to travel.