At a Glance
- Tasks: Coordinate clinical trial sites and build strategic relationships for innovative drug research.
- Company: Join a vibrant Clinical Operations team in a leading research company.
- Benefits: Enjoy flexible work, competitive pay, and great career growth opportunities.
- Other info: Participate in exciting employee events and wellness initiatives.
- Why this job: Make a real impact in clinical research while reducing travel.
- Qualifications: Bachelor's in health-related field and experience in clinical trials required.
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 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 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.
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.
Clinical Trial Site Relationship Coordinator (Hungarian Speaking) employer: Medpace, Inc.
Medpace, Inc. is an excellent employer for those seeking a dynamic role as a Feasibility Data Visualization Analyst in London. With a flexible work environment, competitive compensation, and a strong focus on structured career development, employees are empowered to grow and thrive while collaborating closely with clinical operations and medical teams to enhance data strategies. This supportive culture fosters innovation and meaningful contributions to clinical research.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Trial Site Relationship Coordinator (Hungarian Speaking)
✨Network Like a Pro
Get out there and connect with people in the industry! Attend events, join online forums, and don’t be shy about reaching out to professionals on LinkedIn. Building relationships can open doors that a CV just can't.
✨Ace the Informational Interview
Set up informal chats with folks already working in clinical trials or related fields. Ask them about their experiences and insights. This not only helps you learn but also puts you on their radar for future opportunities.
✨Show Your Passion
When you get the chance to chat with potential employers, let your enthusiasm shine through! Talk about why you love clinical research and how you can contribute to their team. A genuine passion can make you stand out.
✨Apply Directly Through Us
Don’t forget to check out our website for job openings! Applying directly through us not only shows your interest but also gives you a better chance of being noticed by our hiring team. Let’s get you that dream job!
We think you need these skills to ace Clinical Trial Site Relationship Coordinator (Hungarian Speaking)
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 your background fits with what we're looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're excited about this role and how your experience aligns with our needs. Be genuine and let your personality come through – we love seeing the real you!
Showcase Your Communication Skills:Since this role involves building relationships, it's crucial to demonstrate your excellent communication skills in your application. Use clear and concise language, and make sure to proofread for any errors. We appreciate attention to detail!
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 follow the prompts and submit your materials!
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 involves maintaining strategic 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 resolve conflicts.
✨Research the Site Landscape
Before the interview, do some homework on the UK and Hungarian site landscapes. Understanding key opinion leaders, site capabilities, and local medical practices will help you stand out as someone who’s proactive and knowledgeable about the environment you'll be working in.
✨Prepare for Scenario Questions
Expect questions that ask how you would handle specific situations, like site performance issues or feasibility assessments. Think through potential scenarios and how you would approach them, demonstrating your problem-solving skills and strategic thinking.
