The Senior Site Manager will be responsible for maintaining ongoing inspection readiness and compliance with the clinical trial protocol, Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations from study start-up through to site closure
Job Summary
The Senior Site Manager will be responsible for maintaining ongoing inspection readiness and compliance with the clinical trial protocol, Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations from study start-up through to site closure.
Responsibilities include site feasibility and selection, initiation, start-up, monitoring, oversight of key performance indicators, and site/study close-out in complex clinical trials.
The company offers a competitive salary and extensive benefits package, a flexible working environment, and career development opportunities.
Matching Summary
The Senior Site Manager will be responsible for maintaining ongoing inspection readiness and compliance with the clinical trial protocol, Standard Operating Procedures (SOP), Good Clinical Practice (GCP), and applicable regulations from study start-up through to site closure.
Skills & Requirements
Must-have
GCP and regulatory compliance
Site monitoring and oversight
Data accuracy and completeness
Recruitment and retention strategies
Protocol and SOP adherence
Nice-to-have
Strong communication and influencing skills
Problem solver and quick learner
Team player and independent worker
Coaching and mentoring experience
Process improvement participation
Key Requirements
Minimum 3 years clinical trial monitoring experience
BA/BS degree in Life Sciences or related field
Strong understanding of GCP, local laws, and regulations