The Site Partnership mission is to build strong relationships, enhance level of collaboration, and harness input and insights from Investigational sites to drive site performance such as increasing the no. of patients/site, accelerating study start up and reducing overall development milestones through faster patient recruitment. The Site Partnership model will enable early CSU planning to ensure early site relationships exist ahead of future programs and studies. These objectives will be achieved by:
-Providing Transversal Partnership: single point of contact across and in between studies to improve protocol design elements, optimize clinical trial operations, improve site anticipation of upcoming studies, establish effective patient recruitment and retention plans.
-Portfolio Planning: Pro-active review at program and study level with sites to provide sites with ample time to prepare for a new study, including activities that promote early identification of potential study participants and reduce local competition for study subjects. Portfolio planning is also expected to increase the enthusiasm around Sanofi programs and investigational/ post market access products.
-Establishing two way communication between Site & Sponsor: Influencing Protocol design, recruitment strategies, operational efficiencies, decreasing site and patient burden.
-Site Performance: actively review metrics and mutually agree on actions, explore new approaches with sites to drive operational excellence in a changing environment. Exemplifies the culture and expertise to ensure effective site performance and engagement
-Patient Strategy: becomes the main point of contact for patient advocacy related internal/external stakeholders, overlooking the patient centric strategies in clinical development area.
QUALIFICATION
Language skills: Ability to present clear messages accurately in both written and spoken English from complex information/data to all levels in the organization.
Education: University degree in Health Sciences or equivalent
Experience & knowledge: Minimum of 5 years of experience in clinical research
Core competencies: Knowledge of GCP/ICH phase I-IV clinical trials
Management, leadership and communication skills, organizational, analytical and planning abilities, reactivity to emergent needs, able to prioritize, time management.
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