At a Glance
- Tasks: Coordinate clinical trial sites and build strategic relationships to enhance study feasibility.
- Company: Join a vibrant Clinical Operations team in a leading research company.
- Benefits: Exciting career growth, competitive salary, and opportunities to work on innovative drug development.
- Other info: Fluency in English and Hungarian is required; excellent communication skills are a must.
- Why this job: Make a real impact in clinical research while reducing travel and enhancing your skills.
- Qualifications: Bachelor's degree in health-related field and at least 1 year of clinical trials experience.
The predicted salary is between 35000 - 45000 £ per year.
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 Italy. The position is suitable for someone with previous clinical research experience or a CRA looking 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.
- Conduct or expedite feasibility activities (standalone, blinded, initial, ongoing), supporting management with site selection and 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.
- Build and maintain relationships with preferred site networks/flagship sites, including facilitating master CDAs and holding meetings with network directors.
- Conduct regular performance reviews for sites participating in our studies, ensuring quality study delivery.
- Serve as an escalation point for site related issues throughout the life cycle of a study.
- 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.
- Minimum a Bachelor of Science in a health‐related field.
- Minimum 1 year of site and clinical trials experience (more experience for 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.
We kindly ask to send applications in English.
Clinical Trial Site Relationship Coordinator (Italian Speaking) in London employer: Medpace
Join our dynamic Clinical Operations team in London, where we prioritise innovation and employee growth. As a Clinical Trial Site Relationship Coordinator, you'll enjoy a collaborative work culture that values strategic relationships and offers opportunities for professional development in the exciting field of clinical research. With a focus on cutting-edge drug development, we provide a supportive environment that encourages you to thrive while making a meaningful impact.
