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Jodi provides strategic direction and oversees daily operations for ProTrials, including marketing activities, client relations, contract negotiations and resource management. With over 15 years of clinical research and project management experience, she provides vision and guidance to project teams and the senior management team. Prior to founding ProTrials, Jodi gained extensive experience in both pharmaceutical and device clinical trials as a CRA and project manager at Syntex, Inc., as an international project manager for Otsuka America, and as a project manager for programs in multiple countries including the United States, Japan, Thailand, Spain and Canada. She is an active member of many organizations including the Drug Information Association, The Alliance of CEOs, and The National Association of Women Business Owners Inger provides strategic direction and oversees daily operations for ProTrials, including management of financial operations, client relations, resource management and HR, and IT operations. With over 23 years of clinical research and project management experience, she provides vision and guidance to project teams and the senior management team. Prior to founding ProTrials, Inger gained extensive experience in pharmaceutical clinical trials as a CRA, Clinical Research Manager and Team Leader for Syntex, Inc. and Roche Pharmaceuticals, with experience in North America and Europe involving cardiovascular, infectious disease, gastroenterology, reproductive, anti-inflammatory, central nervous system, dermatology, and rheumatology products. She is an active member of a number of organizations including Drug Information Association, Association of Clinical Research Professionals and The National Association of Women Business Owners. Janie joined ProTrials in 1998, and leads clinical operations activities in the Western United States. Janie’s responsibilities include the implementation of quality systems and tools throughout the company, line management, staff education, business development, and client relations. With 15 years of industry experience, Janie brings to ProTrials a strong clinical focus, and provides direction for growth of the organization, as well as for development of individual staff members. Prior to joining ProTrials, Janie worked for Syntex, Inc. and Clinimetrics (CRO), providing project management for global pharmaceutical and medical device trials while based in Italy, England and California. Her experience includes a broad range of therapeutic indications, and the successful implementation of clinical trials across multiple continents.
Jolyn joined ProTrials in 1997, and is responsible for overseeing Human Resources policies and procedures, employee benefits, standard operating procedures and general office operations. She is an active member of the SOP writing team and has been a valued member of the Core Management Team since its inception in 2002. In addition to her extensive administrative and finance experience, Jolyn spent 11 years as a Clinical Research Associate at Pharmaquest, Syntex, Inc., and Chiron, where she gained in-depth experience with federal and international regulations
Wendy joined ProTrials in 1997, and is actively involved in clinical operations in the western region of the United States. Wendy has a variety of responsibilities such as development and implementation of employee training programs, line management, marketing and business development, client management, and building company-wide infrastructure. Wendy has over 14 years of experience in the pharmaceutical and health care industries. During this time, Wendy has gained in-depth expertise in international and domestic clinical trial management, clinical quality assurance compliance, CRO selection, partnering, client relations, business development, and NDA filings. Prior to joining ProTrials, she held management positions at Syntex, Inc., Roche Pharmaceuticals, and CV Therapeutics Inc.
Carol joined ProTrials in 1999, and is responsible for directing the company’s business operations and regional staff throughout the Eastern United States. With over 25 years of experience in the clinical research field, Carol uses her unparalleled industry expertise to build strong teams and implement efficient and effective operational procedures. Prior to joining ProTrials, she worked at Sponsor and CRO companies including Genentech, Syntex, Inc., and Parexel where she had direct responsibility for activities including personnel and budget management, study site monitoring, project management, regulatory affairs, training, and business development. She is an active member of Drug Information Association, and past member of the Project Management Institute and Regulatory Affairs Professionals.
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