Associate Project Manager - Bellville

Job Overview

• 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.

Requirements

• 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.