Global Site Id Mgr

hace 1 semana

Desde casa, México IQVIA A tiempo completo

**Job Overview**
Develop and implement department procedures and manage overall team. Directs activities for the Feasibility and Site Identification component of designated projects within the country, region or function, in accordance with the scope of work and contracted timelines in line with the Feasibility and/or Site Identification portion of the study budget. Lead and/or support the formulation, implementation, and operational integration of strategic and departmental goals and objectives.

**Essential Functions**
- Lead and/or support the formulation of strategic initiatives and work with functional management to develop implementation plans, including Feasibility and/or Site Identification evaluation measures. Interface with internal contacts to determine operational strategy and/or expectations and parameters for key deliverables. Provide Proposal Management with input on proposals and budget development for Feasibility/Site ID components of projects. Attend proposal defenses as needed. Liaise with internal/external clients to ensure operational efficiency
- implement updates to processes to ensure maximum efficiency and customer satisfaction. Review and analyze performance metrics and processes to provide input in the development and implementation of process/system improvements. Accountable for employee departmental efficiency and adherence to standard operating procedures (SOPs), Work Instructions, and project instructions and timelines. Manage employees in accordance with organization’s policies and applicable laws. Responsibilities include planning, assigning and directing work of employees
- appraising performance and guiding professional development
- rewarding and disciplining employees

**Qualifications**
- Bachelor's Degree Life sciences or related field.
- 5-6 years' relevant experience including demonstrable experience in acting as the main** global** lead in studies.
- Strong negotiation and communication skills with ability to challenge
- Excellent interpersonal skills and strong team player
- Proven ability to work through others to deliver results to the appropriate quality and timeline metrics on complex projects
- Thorough understanding of regulated clinical trial environment and in depth knowledge of drug development process
- Demonstrated proficiency in using systems and technology to achieve work objectives
- Good regulatory and/or technical writing skills
- Good leadership skills, with ability to motivate, coach and mentor
- Good organizational and planning skills
- Ability to exercise independent judgment taking calculated risks when making decisions
- Good presentation skills
- Proven ability to establish and maintain effective working relationships with co-workers, managers and sponsors.
- Excellent understanding of study financial management
- Proven ability to work on multiple projects balancing competing priorities

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