Tina Miller
Executive Director @Syneos Health Clinical Solutions
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WORK HISTORY
Executive Director @Syneos Health Clinical Solutions
US
Oversees and leads the strategic aspects of the Global Functional Service Provider (FSP) models, working with operational leads to execute and achieve target revenue and profitability while ensuring the contracted services and expectations of all projects are carried out by the assigned project teams in accordance with executed contracts and customer expectations. Duties include strong internal and external relationships with primary FSP customers, leaders, strong operational strategic guidance, understanding of staff utilization and realization of project revenue, support of growing resourcing models, guidance on improvements of processes and procedures, and strong management skills and industry knowledge in the FSP space. The Exec Dir, Global FSP360 is responsible for partnering with operational leads to design strategic solutions to support Global Functional Service Provider models in order to drive profitable driving profitable growth for the FSP Business Unit. The Exec Dir, Global FSP360 represents the FSP business across assigned accounts and/or a singular function to ensure that robust strategic growth plans are developed and attained. Exec Dir, Global FSP360 is responsibilities include development of solid strategic plans to drive growth, solutions design, development and oversight. The incumbent also involves the necessary parties in the development and execution of those plans. The successful incumbent will expand and maintain relationships and is responsible for driving profitable growth. Exec Dir, Global FSP360 will operate in a transparent, proactive, collaborative environment. Company ethical standards and policies will be upheld.
SKILLS
ABOUT TINA MILLER
Almost 27 years of clinical research experience, 22 years in clinical research management. Experience managing clinical research personnel including Associate Directors, Regional Managers, Clinical Project Leads, Site Care Partners, Clinical Research Associates (CRAs), Clinical Research Site Managers (CRSMs), LCRAs, Monitoring Process Trainer, Technical Trainer, and Territory Development Specialists. Clinical trial experience includes monitoring, including implementation of study protocols with special emphasis on compliance with FDA regulations and on-site data management and collection. Therapeutic areas of experience include Diabetes, Alzheimer’s Disease, Rheumatoid Arthritis, Osteoarthritis, HIV, Antifungals, Cardiovascular, Antihistamines, Antidepressants, Antihyperlipidemic Agents, Vaccines, Allergy, Respiratory, Inflammation and Ophthalmology.
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