Clinical Trials Site Relationships Lead — Madrid

Medpace, Inc.; Madrid; Presencial; EUR 42.000 - 64.000; Jornada completa

Descripción de la vacante

Medpace, Inc. in Madrid, Spain, is seeking a full-time Clinical Trial Site Relationship Coordinator to join our Clinical Operations team. You will work on pre-award and post-award feasibilities, build and maintain strategic site relationships, and help develop strategies to conduct feasibilities in Spain.

Ideal candidates have prior clinical research experience or CRA background with tolerance for travel. You will support site selection, feasibility activities, and ongoing site performance,

Formación

• Bachelor of Science in health-related field required.
• At least 1 year of site and clinical trials experience.
• CRA experience is an asset.
• Knowledge of drug development, clinical trial management and operational procedures.
• Knowledge of medical terminology and patient management preferred.
• Fluency in English and Spanish.
• Demonstrated organizational and prioritization skills.
• Excellent oral and written communication skills.
• Proficient with Microsoft Office applications.

Responsabilidades

• Provide ongoing support of sites, including identifying future business opportunities and feasibility assessments.
• Develop plans for site contact and follow-up.
• Support expediting feasibility, site selection and study start-up; and
• May be responsible for other projects and responsibilities as assigned.
• Serve as site relations and excellence partner by providing oversight and building/retaining relationships of assigned sites within assigned country.
• Conducting/expediting feasibility activities (standalone, blinded, initial, ongoing), supporting Management with site selection/alignment with studies and/or therapeutic areas, and study start-up.
• Proactively research and understand specified site landscape/intelligence (KOL presence and knowledge, site capabilities, country standard of care and medical practices, etc.) as it relates to specific patient population, recruitment, and retention.
• Building and maintaining relationships with preferred site networks/flagship sites which includes facilitating master CDAs and holding meetings with network directors
• Conducting regular performance reviews for sites participating to our studies, ensuring quality study delivery
• Serve as an escalation point for site related issues throughout the life cycle of a study
• Provide ongoing support of sites, including identifying and discussing future new business;
• Develop effective plans for site contacts, troubleshooting, and follow-up;
• Develop an intelligence database with site and country intelligence
• Support Management with process improvement initiatives regarding feasibility activities
• Serve as main point of contact for project teams regarding site performance issues and updates on pertinent site information; and
• May be responsible for other projects and responsibilities as assigned, including site Qualification Visits, prepping/consultation support for site audits, etc.

Conocimientos

Site relationship management

Clinical trials

Feasibility studies

Communication skills

GCP knowledge

MS Office

English fluency

Spanish fluency

Project coordination

Educación

Bachelor of Science in health-related field

Herramientas

Microsoft Office

Descripción del empleo

Medpace, Inc. in Madrid, Spain, is seeking a full-time Clinical Trial Site Relationship Coordinator to join our Clinical Operations team. You will work on pre-award and post-award feasibilities, build and maintain strategic site relationships, and help develop strategies to conduct feasibilities in Spain.

Ideal candidates have prior clinical research experience or CRA background with tolerance for travel. You will support site selection, feasibility activities, and ongoing site performance,