Job Opportunity
We are seeking a senior site management professional to serve as the sponsor's interface with the investigative site and a member of the local study management team.
About This Role:
* Manage all aspects of site management from pre-trial assessments through to database locks and close-out activities.
Requirements:
* Bachelor's degree in science, nursing or life sciences.
* Minimum 3 years on-site clinical trial monitoring experience preferred.
* Experience in monitoring early phase haematology and oncology studies preferred.
* Demonstrated success as a clinical research associate.
* Excellent communication and problem-solving skills.
* Strong working knowledge of company standard operating procedures, local laws and regulations, and assigned protocols.
* Strong understanding of good clinical practice and local regulatory guidelines.
* Proficient in using relevant IT software applications and company systems.
* Willingsness to travel for work purposes.
Why Us?
* Competitive compensation package and ongoing training opportunities.
* Award-winning leadership development programs.
* Inclusive, flexible, and accessible work arrangements.
* Equal opportunity employer supporting diversity and inclusion.