Assoc Prime Site Manager
hace 4 meses
**Job Overview**
Works under moderate supervision to build and maintain partnerships at IQVIA Prime and partner sites to streamline startup processes, maximize the recruitment of patients into trials whilst adhering to high quality standards and improving the experience of patients, site staff and customers working with IQVIA. In liaison with key stakeholders at site and at IQVIA, to promote a growth and differentiation strategy, to collaborate on innovation in clinical research, to build expanded capability, to drive productivity and maintain robust quality management. Be an advocate for IQVIA Strategic sites.
May act as a dual role as CRA Line Manager and/or mentor of CRAs trainee.
**Essential Functions**
- Manage Prime and partner site located in Argentina. Works under moderate supervision to develop new alliance site and maintain the cooperation.
- May act as a dual role as CRA Line Manager and/or mentoring of CRAs trainee, including training and development of staff.
As Prime/Partner Site Manager you will:
- Support implementation of the IQVIA Prime Site strategy, works under moderate supervision to maximize site productivity, concentrating on recruiting more patients from fewer sites whilst maintaining high quality standards.
- Support the enhancement of the experience of patients, site staff and customers working with IQVIA through Prime/Partner Sites.
- With guidance, implement the IQVIA Prime Site strategic plan promoting growth and differentiation, working with the site to execute the strategic imperatives of the plan. This will include site non-project specific strategies e.g. study start up processes, patient recruitment methodologies, infrastructure and capabilities enhancement, strengthening and alignment of recruitment pipelines and leveraging innovation to advance clinical research.
- Maintain and share metrics as well as pipeline information with the prime sites on a routine basis.
- Support identification of opportunities for Prime Sites to participate in studies that match site capabilities, by collaborating with therapeutic area/project strategy teams. Work to adjust prime site capabilities to IQVIA available study portfolio, actively liaising with internal and external stakeholders.
- Collaborate with other IQVIA team members, working with the prime/partner sites, to overcome any site related barriers and challenges that affect the ability of the site to produce quality project deliverables in an effective, efficient and timely manner.
- Share information and provide efficient communication with delivery teams, resolve site issues that have been escalated by the CRA or project teams.
- Ensure IQVIA processes integrate with those of the site. Support adoption of IQVIA systems by sites, or with support, create and execute guidance and solutions for internal teams when this is not possible.
- Perform other duties as assigned.
**Qualifications**
- Bachelor's Degree in a scientific or healthcare discipline
- ** 5 years** of prior clinical trial experience
- Preferrable experience in leadership capacity
- In-depth knowledge of applicable clinical research regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).
- 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 investigational sites.
- Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint.
- Availability to travel (eventually)
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