About the job
Timeline Optimization's mission is to help job seekers find attractive opportunities before they become widely advertised. We are not a staffing firm or agency. Timeline Optimization does not hire directly for these positions—we identify and validate them in real-time from actual employers.
Employer Industry: Pharmaceutical Research and Development
Why Consider This Job Opportunity
- Salary up to $80,000 annually
- Comprehensive benefits package, including health, dental, and vision insurance
- 401(k) plan with employer match to support your future
- Opportunities for professional training and development
- Paid vacation, holidays, sick leave, and bereavement leave
- Collaborative work environment focused on employee development and well-being
What To Expect (Job Responsibilities)
- Schedule all protocol-required tasks for in-life studies and manage departmental study schedules
- Create daily task schedules based on study needs and employee availability
- Coordinate with other departments to address logistical challenges related to study tasks
- Assist with verification and posting of generated schedules
- Troubleshoot and resolve logistical challenges associated with workload and study execution
What Is Required (Qualifications)
- Bachelor of Arts (BA), Bachelor of Science (BS), or prior relevant experience
- Minimum of 3 years working in a research environment, preferably in a GLP setting
- Proficient in Microsoft Office Suite, including Word, Excel, and PowerPoint
- Strong organizational skills and ability to multi-task in a fast-paced environment
- Excellent attention to detail and ability to communicate effectively with all levels of management