A company is looking for an Integrated Study Timeline Implementation Manager to lead the development and maintenance of Integrated Study Timelines for clinical trials.
Key Responsibilities
Provide expertise in creating timelines using integrated study timeline templates
Coordinate and lead discussions for timeline customization and maintenance
Monitor project progress, identify delays, and update stakeholders on timeline changes
Required Qualifications
Bachelor's Degree or international equivalent, preferably in Life Sciences
Over 5 years of experience in the pharmaceutical industry or clinical research organization
3+ years of experience in clinical study management or oversight
Proficient in Microsoft Project (MSP) with 3+ years of experience using the tool
Knowledge of global regulatory compliance requirements for clinical research
Clinical Project Manager • Orange, California, United States