Effectively communicate with internal and external customers as well as third party vendors
Oversee and / or manage study start-up activities as applicable
Review and provide input into patient recruitment plan and retention plan
Monitor study timelines, patient recruitment, retention and data cleaning to ensure successful outcome of the project
Collaborate with project team and relevant vendors on database lock activities
Maintain a working knowledge and ensure compliance with applicable ICH-GCP Guidelines, local regulatory requirements and Parexel WSOPs, SOPs, Operational Guidelines
Requirements
Proven clinical experience or management experience in healthcare, clinical research, or contract research organization
Substantial experience in clinical research including relevant experience as a team Leader in Clinical functions or proven experience in coordinating clinical trials
Strong command of written and spoken English language, local language proficiency as required
Ability to travel as required.
Degree in a life science, nursing qualification or relevant clinical and or clinical management experience