Clinical Trial Site Relationship Coordinator (Hungarian Speaking)

Medpace; Greater London; On-site; GBP 42,000 - 58,000; Full time

Job summary

Medpace is seeking a full-time Clinical Trial Site Relationship Coordinator to join our Clinical Operations team in London. You will manage site networks, support feasibility activities, and help drive study start-up across the UK and Hungary.

Ideal candidates have clinical research experience or CRA background, with English and Hungarian fluency, and strong organizational and communication skills. The role offers growth opportunities within Medpace’s global CRO framework.

Qualifications

• Bachelor of Science in a health-related field is required.
• At least 1 year site and clinical trials experience; more for senior roles.
• CRA experience is an asset.
• Knowledge of drug development, clinical trial management, and GCP preferred.
• Fluency in English and Hungarian.
• Strong organizational and prioritization skills.
• Excellent oral and written communication skills.
• Proficient with Microsoft Office applications.

Responsibilities

• Provide ongoing site support and identify future business opportunities and feasibility assessments.
• Develop effective plans for site contact and follow-up.
• Support expediting feasibility, site selection and study start-up.
• Serve as site relations and excellence partner for assigned sites and country.
• Conduct feasibility activities and assist with site selection/alignment with studies.
• Proactively research site landscape, data, and country intelligence related to patient populations and recruitment.
• Build and maintain relationships with flagship sites and manage meetings with network directors.
• Conduct regular performance reviews for sites and ensure quality study delivery.
• Act as escalation point for site-related issues during a study lifecycle.
• Assist with process improvements in feasibility activities.
• Be the main contact for project teams regarding site performance updates.

Skills

English fluency

Hungarian

Organizational skills

Communication skills

Microsoft Office

Education

Bachelor of Science in health-related field

Tools

Microsoft Office

Job description

About the Role

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 London. This is a fantastic opportunity to work on pre-award and post-award study feasibilities, build and maintain strategic relationships with our network of sites, and develop key strategies to effectively conduct feasibilities in the UK and Hungary. 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
• 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
• May be responsible for other projects and responsibilities as assigned, including site Qualification Visits, prepping/consultation support for site audits, etc.

Qualifications

• 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; Hungarian
• Demonstrated organizational and prioritization skills
• Excellent oral and written communication skills
• Proficient knowledge of Microsoft Office applications

Why Work at Medpace?

At Medpace, you will find work that is both challenging and rewarding. 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.

What to Expect Next

We look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an initial phone interview.

About Medpace

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 6,000 people across 40+ countries.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Medpace is an equal opportunity employer.