The role involves providing leadership to clinical site management teams from study start through closure while serving as the primary point of contact for sponsors and investigators
Job Summary
The role involves providing leadership to clinical site management teams from study start through closure while serving as the primary point of contact for sponsors and investigators.
Candidates must demonstrate initiative by identifying obstacles and offering solutions to ensure compliance with the Clinical Monitoring Plan and study budgets.
Worldwide Clinical Trials is a global midsize CRO committed to cultivating a diverse, inclusive environment where professionals can thrive by being themselves.
Matching Summary
The role involves providing leadership to clinical site management teams from study start through closure while serving as the primary point of contact for sponsors and investigators.
Skills & Requirements
Must-have
Lead clinical site management team
Manage monitoring deliverables and budget
Proficiency in CTMS and EDC systems
Experience as Senior Clinical Research Associate
Strong communication in English and local language
Nice-to-have
Remote team leadership capabilities
Proactive problem-solving skills
Collaborative and inclusive work environment
Hands-on accessible leadership style
Key Requirements
Minimum 3 years experience as Senior Clinical Research Associate
Four-year college degree in biological, physical, or health studies
Two-year college curriculum with nursing or life science degree preferred