Coordinator (m/w/d) Projects

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7l0rt4

Our clinical activities are growing rapidly, and we are currently seeking a full-time Clinical Trial Site Relationship Coordinator to join our vibrant Clinical Operations team in Italy, Milan. This position will fit someone who has previous clinical research experience or perhaps a CRA who would like to reduce travel. If you want an exciting career within a company that excels in delivering innovative research and development of cutting edge drugs, where you can grow your potential, then this is the opportunity for you.

Provide ongoing support of sites, including identifying and discussing future new business opportunities and feasibility assessments

- Support management in expediting feasibility, site selection and study start-up
- 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 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 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
- May be responsible for other projects and responsibilities as assigned, including site Qualification Visits, prepping/consultation support for site audits, etc. Minimum a Bachelor of Science in health-related field
- Minimum 1 years' site and clinical trials experience (more experience for the more senior positions required)
- CRA experience is an asset
- Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines preferred
- Knowledge of medical terminology and clinical patient management preferred
- Fluency in English
- Proficient knowledge of Microsoft Office applications. We kindly ask to send applications in English. At Medpace, you will be given the tools and training to succeed. At Medpace, you will be rewarded for strong performance and provided opportunities to grow professionally. If interested,



you will be contacted for an initial phone interview. Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through the advancement of clinical research. We leverage in-country regulatory and therapeutic expertise across all major therapeutic areas including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, we employ more than 6,500 people across 40+ countries. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration. Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence Office based environment with on-site mentors - Industry renowned onboarding and training programs designed to accelerate professional development - Ongoing training and continuous learning opportunities throughout your career - Other Employee Benefits - - Comprehensive health, wellness, retirement, and PTO benefits - Office based culture with occasional WFH that provides flexibility for eligible positions after training - Please note benefits may vary based on country.

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/7l0rt4