Clinical Trial Liaison - Mexico en Syneos Health

Clinical Trial Liaison - Mexico
Syneos Health
INC Research is a therapeutically focused global clinical research organization (CRO)
providing a complete range of Phase I ? Phase IV clinical development services for the
world?s biopharmaceutical companies. Our mission is to help our customers bring
products to market to improve world health.
INC Research provides significant scale, scope and expertise to deliver innovative clinical development
approaches and strategic alliances that meet the needs of our customers. In July 2011, INC Research acquired
Kendle International, a leading global CRO, to create a new enviable force in global
Acapulco, Aguascalientes, Campeche, Cancún, Ciudad Juárez, Ciudad Victoria, Colima, Cuernavaca, Culiacán, Chetumal, Chihuahua, Chilpancingo, Durango, Guadalajara, Guanajuato, Hermosillo, Jalapa, La Paz, León, Mérida, Mexicali, México DF, Estado de México, Monterrey, Morelia, Oaxaca, Pachuca, Puebla, Querétaro, Saltillo, San Luis Potosí, Tepic, Tijuana, Tlaxcala, Toluca, Torreón, Tuxtla Gutiérrez, Veracruz, Tabasco, Zacatecas, 30 Jul.
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Descripción
Overview

Base Location: Mexico Regions Covered: Mexico, Chile, Colombia, Argentina

The Clinical Trial Liaison is responsible for providing non-promotional scientific, educational, and research support for client’s clinical studies. The CTL should be highly trained in assigned therapeutic area and well-versed in clinical research and practice. A primary focus of this role and basis for measuring CTL performance is the ability to identify appropriate patients with Agitation in Alzheimer’s Disease (AAD) and their treating physicians, support acceleration of clinical studies completion through identification of new clinical sites, collaboration with existing sites, and/or enrollment of appropriate patients in client-sponsored clinical trial.

Responsibilities

• Establishes and maintains strong working relationships with Principal Investigators (PIs) and clinical trial sites to support the enrollment and conduct of clinical studies
• Works with internal Clinical Development and Clinical Operations leads and trial sites to understand and implement study protocols effectively; partners with sites to develop and implement effective local and regional subject recruitment strategies, facilitate escalation of investigator questions/concerns, recruitment/retention initiatives and clinical site & investigators meetings as it relates to recruitment strategies
• Develops a network and heat maps of HCPs/hospitals involved in study specific diagnosis and management of patients
• Adhere to regulatory and compliance guidelines and company policies.

Numero de vacantes: 1
Tipo de contrato: Indefinido
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Requisitos
• Advanced degree in clinical specialty (PharmD, PhD, MD) with clinical experience
• 5+ years’ experience as an MSL/CTL or senior clinical development role
• 3+ years CNS (ideally Alzheimer) experience required
• Experience in clinical research, patient recruitment, and investigator sponsored trials
• Self-starter, highly accountable, and skilled problem solver
• Very good understanding of networking and patient enrolment strategies
• Willingness to travel extensively across a number of regions

Estudios mínimos
Licenciado
Idiomas
Inglés nivel Alto.
Experiencia mínima
5 años
Disponibilidad para viajar
El 80% del tiempo laboral



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