Assoc Manager, Regulatory & Start Up (FSP)

at  IQVIA

JOB OVERVIEW

Supervises a local work unit responsible for local regulatory activities. Sets day-to-day operational objectives for team, focusing on mentoring, coaching, and work flow coordination.

QUALIFICATIONS

• Bachelor’s Degree Scientific discipline or health care preferred.
• Typically requires a minimum of +3 years of prior relevant experience within the Regulatory & Start Up/ Site Activation / Site Management area.
• Previous experience leading teams and management tasks, either formal or at a project level.
• Advanced level of English.
  IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.co

• Manages staff’s delivery of local regulatory activities in accordance with organization’s policies and applicable regulations. Responsibilities include planning, assigning, and directing work, assessing performance, and guiding professional development, rewarding and disciplining employee, and addressing employee relations issues and resolving problems.
• Participate in the selection process for hiring new employees by conducting candidate review and participating in the interviewing process. Ensure that new employees are properly onboarded and trained.
• 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, as applicable.
• Participate, as required, in the allocation of resources to clinical research projects by assigning staff based on their experience and training.
• Manage the quality of assigned staff’s work through regular review and evaluation of work product.
• Ensures that staff are meeting defined workload and quality metrics through regular review and reporting of findings as outlined by clinical operations management.