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About the Role
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.
Responsibilities
- Provide ongoing support of sites, including identifying and discussing future new business opportunities and feasibility assessments
- Develop effective plans for site contact and follow-up
- Support management in expediting feasibility, site selection and study start-up
- 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
- May be responsible for other projects and responsibilities as assigned, including site Qualification Visits, prepping/consultation support for site audits, etc.
Requirements
- 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
- Fluency in Hungarian
- Demonstrated organizational and prioritization skills
- Excellent oral and written communication skills
- Proficient knowledge of Microsoft Office applications
- Applications to be sent in English
Location
- London
Work Type
- Full-time
Experience Level
- Minimum 1 years' site and clinical trials experience
Education Level
- Bachelor of Science in health-related field
Benefits
- Competitive compensation programs that recognize and reward performance
- Comprehensive health, wellness, retirement, and PTO benefits
- Office based culture with occasional WFH that provides flexibility for eligible positions after training
- Company-sponsored social events
About the Company
- 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.
- Purpose-Driven Work: Work alongside physicians, scientists, and industry-leading experts committed to advancing the global development of medical therapeutics through clinical research excellence
- Collaborative Culture: Contribute to an interactive team environment that empowers decision making, creative thinking, and continuous learning through open communication and mutual trust.
- Leadership throughout Medpace is both accessible and approachable
- Continuous Growth & Development: Office based environment with on-site mentors
- Defined career paths with clear advancement opportunities
- Industry renowned onboarding and training programs designed to accelerate professional development
- Ongoing training and continuous learning opportunities throughout your career
- An environment that encourages employees to influence change, contribute ideas, and grow quickly