Clinical Study Manager (San Antonio, Tx)
About The Position
The Clinical Study Manager (CSM) will manage one or more allocated Phase I through IV Clinical Trials that may be local, regional or global in scope. Worldwide Clinical Trials (WCT) Clinical Study Managers are 100% accountable for the success of their projects: Clinical Study Manager (CSM) is responsible for the overall coordination and management of clinical trials from start up through close out activities. Directs the technical, financial and operational aspects of the projects to secure the successful completion of clinical trials. Works with functional area leads to identify and evaluate fundamental project requirements, interpret data on complex issues, is responsible for contingency planning and implementation of rescue strategy where needed and ensure solutions are implemented. The CSM works to ensure that all project deliverables meet the customer’s time/quality/cost expectations. The CSM, with support from the Project Management Directors, working in collaboration with other functional area leads, is accountable for ensuring that all project deliverables meet the customer/contract expectations. The Clinical Study Manager works under the direct supervision and guidance of the Site Director. He/she is not responsible for supervising other staff.
Requirements
- University/college degree (life science preferred) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology) or equivalent combination of education and experience that provides the individual with the required knowledge, skills and abilities
- Experience in managing projects in a multi-office environment
- Demonstrated ability to handle multiple competing priorities; utilize resources effectively
- Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system
- Demonstrated ability to lead by example and to encourage team members to seek solutions
- Excellent communication, planning and organizational skills
- Self-motivated and excellent problem solving skills
Nice To Haves
- Minimum of five (5) years of clinical pharmaceutical industry experience including demonstrated skills and competency in clinical project management tasks
Responsibilities
- Lead core project team members and facilitate their ability to lead extended/complete project team
- Lead cross unit coordination both internal and external, inclusive of sub-contractors
- Define and manage project resource needs in conjunction with functional heads and establish contingency plans for key resources
- Ensure successful design, implementation, tracking and revision of project plans for assigned projects
- Promote effective teamwork among project team members; resolve conflicts as needed
- Ensure appropriate communication on project-related matters with the CSM Management
Benefits
- competitive benefits package
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
