Clinical Research Site Leader

The clinical research site leader is responsible for providing administrative and operational oversight for the implementation of multiple clinical trials at the site. Key responsibilities include site management, stakeholder collaboration, staff supervision, meeting study deliverables, reporting, maintaining standard operating procedures (SOPs), and supporting team development.

KEY SUMMARY OF POSITION :

(For the sake of brevity and easy reading, only a key summary of the full job specification / job advert as provided by the client is provided below. Additional information and full details regarding the position and potential employer will be provided following our initial contact and the CV review)

PROJECT MANAGEMENT

• Lead and oversee multiple clinical studies, ensuring adherence to GCP, protocols, SOPs, and sponsor / internal standards; standardize study processes across planning, activation, recruitment, data management, and closeout phases.
• Monitor study performance, address findings from monitoring reports with PIs, maintain essential documents, provide stakeholder updates, engage with communities, and contribute to SOP development.

SITE MANAGEMENT

STAFF TRAINING & MENTORSHIP

RESEARCH OUTPUTS

QUALIFICATIONS AND REGISTRATION

EXPERIENCE

OTHER REQUIREMENTS

SALARY :

This role is open to candidates at varying levels, and the final remuneration package will be tailored to reflect your individual qualifications, skills, and experience.