At a Glance
- Tasks: Coordinate clinical trial sites and build strategic relationships in the UK and Hungary.
- Company: Join a vibrant Clinical Operations team at a leading research company.
- Benefits: Flexible work environment, competitive pay, and structured career growth opportunities.
- Other info: Exciting opportunities for professional development and employee wellness initiatives.
- Why this job: Make an impact in innovative drug development while enjoying a supportive work culture.
- Qualifications: Bachelor's in health-related field and experience in clinical trials preferred.
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 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 in 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.
- Minimum a Bachelor of Science in health‐related field;
- Minimum 1 year's 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.
- 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.
Clinical Trial Site Relationship Coordinator (Hungarian Speaking) in London employer: Medpace, Inc.
Join our dynamic Clinical Operations team in London as a Clinical Trial Site Relationship Coordinator, where you will thrive in a supportive and innovative environment. We offer a flexible work culture, competitive compensation, and structured career paths that empower your professional growth while you contribute to groundbreaking research in drug development. With a focus on employee wellness and appreciation, this role provides a unique opportunity to build meaningful relationships within the clinical trial landscape in both the UK and Hungary.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Trial Site Relationship Coordinator (Hungarian Speaking) in London
✨Network Like a Pro
Get out there and connect with people in the clinical research field! Attend industry events, join relevant online groups, and don’t be shy about reaching out to potential colleagues on LinkedIn. Building relationships can open doors to opportunities that aren’t even advertised.
✨Show Off Your Skills
When you get the chance to chat with hiring managers or recruiters, make sure to highlight your clinical trial experience and any specific skills that relate to the role. Be ready to share examples of how you've successfully managed site relationships or conducted feasibility assessments.
✨Follow Up Like a Boss
After interviews or networking events, send a quick follow-up message to thank them for their time and reiterate your interest in the position. This not only shows your enthusiasm but also keeps you fresh in their minds when they’re making decisions.
✨Apply Through Our Website
Don’t forget to check out our website for the latest job openings! Applying directly through our site can sometimes give you an edge, as it shows your commitment to joining our team. Plus, you’ll find all the info you need about the roles we’re offering.
We think you need these skills to ace Clinical Trial Site Relationship Coordinator (Hungarian Speaking) in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Clinical Trial Site Relationship Coordinator role. Highlight your clinical research experience and any relevant skills that match the job description. We want to see how you fit into our vibrant team!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're excited about this opportunity and how your background makes you the perfect fit. Don’t forget to mention your fluency in Hungarian – it’s a big plus for us!
Showcase Your Communication Skills:Since excellent communication is key in this role, make sure your written application reflects that. Keep it clear, concise, and professional. We love seeing candidates who can express themselves well on paper!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it’s super easy – just a few clicks and you’re done!
How to prepare for a job interview at Medpace, Inc.
✨Know Your Clinical Research Stuff
Make sure you brush up on your clinical research knowledge, especially around drug development and GCP guidelines. Being able to discuss your previous experiences and how they relate to the role will show that you're not just a good fit, but that you’re genuinely interested in the field.
✨Show Off Your Relationship-Building Skills
Since this role is all about maintaining relationships with sites, think of examples where you've successfully built or managed relationships in the past. Be ready to share specific stories that highlight your communication skills and ability to work collaboratively.
✨Research the Site Landscape
Before the interview, do some homework on the UK and Hungarian clinical trial landscape. Understanding key opinion leaders, site capabilities, and local medical practices will help you stand out as someone who’s proactive and knowledgeable about the industry.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific situations, like resolving site-related issues or expediting feasibility activities. Think through potential scenarios and how you would approach them, demonstrating your problem-solving skills and strategic thinking.
