Facilitate study setup, including protocol and budget review, leading meetings, and developing project plans.
Partner with the Study Setup team for quality database setup and oversee protocol documentation.
Prepare and present protocol-specific materials at Kick Off and Investigator meetings.
Monitor project plans, timelines, and deliverables, manage documentation, and oversee study monitoring and reporting.
Manage study scope changes and budget monitor quality of the study and any service-related issues, implementing changes as required.
Collaborate with project management to improve processes and service quality.
Coordinates company services, such as but not limited to, database setup, data management, and lab operations, and serves as a resource for internal departments.

Bachelor’s degree in Life Sciences and/or related field preferred
Equivalent combinations of education, training, and experience may be considered.
Knowledge of project management methodologies, processes, and best practice technology.
Minimum of 18 months experience in a project management and customer-facing environment preferred.
Over 2 years of experience in the clinical or research industry preferred.
Skill in creating and maintaining project timelines to ensure deadlines are met.
Experience in managing project budgets to avoid cost overruns.
Ability to achieve results through collaborative efforts with others.
Knowledge of Laboratory Operations, and Central Laboratory Functions (kits/supplies, logistics, specimen storage, data reporting, site alerts, etc.)
Ability to identify potential risks and develop mitigation strategies.
Experience in successfully leading large, global, and complex Phase I-IV clinical trials preferred.

Associate Project Manager

Key skills