Lead complex internal investigations related to ethical breaches and misconduct across Latin America at PPG. Collaborate with global partners and ensure adherence to Code of Conduct.
About the role
- Manage a team of clinical staff working in support of clinical studies at IQVIA. Ensure projects are appropriately resourced and employees are trained for success.
Responsibilities
- Manage a team of clinical staff working in support of clinical studies to ensure projects are appropriately resourced and employees are trained and meeting project objectives
- Manage staff in accordance with organization’s policies and applicable regulations
- Participate in the selection for hiring new employees by conducting candidate review and participating in the interviewing process
- Ensure that staff has the proper materials, systems access and training to complete job responsibilities
- Provide oversight for the execution of the training plan, SOP review and training experiences
- Participate in the allocation of resources to clinical research projects by assigning staff to clinical studies based on their experience and training
- Manage the quality of assigned staff's clinical work through regular review and evaluation of work product
- Identifies quality risks and issues and create appropriate corrective action plans to prevent or correct deficiencies in performance of staff
- Ensures that staff are meeting defined workload and quality metrics through regular review and reporting of findings as outlined by clinical operations management
- May collaborate with other clinical teams and other functional leadership to manage project related challenges and to achieve exemplary customer service
- Participates in corporate or organizational departmental quality or process improvement initiatives.
Requirements
- Bachelor's Degree in scientific discipline or health care preferred
- Prior clinical trial experience including experience in a management/leadership capacity or equivalent combination of education, training and experience
- In-depth knowledge of applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines)
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
- Written and verbal communication skills including good command of English
- Excellent organizational and problem solving skills
- Effective time management skills and ability to manage competing priorities
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
Benefits
- Health insurance
- Professional development opportunities
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Tech skills
Location requirements
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