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- Tasks: Coordinate clinical trial sites and build strategic relationships for innovative drug research.
- Company: Join Medpace, a leading clinical contract research organisation with a global impact.
- Benefits: Enjoy flexible work, competitive pay, and structured career growth opportunities.
- Other info: Be part of a team recognised for excellence and innovation in clinical research.
- Why this job: Make a difference in healthcare while developing your skills in a dynamic environment.
- 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 seeking a full-time Clinical Trial Site Relationship Coordinator to join our Clinical Operations team in London. This role involves pre-award and post-award study feasibilities, building and maintaining strategic relationships with our network of sites, and developing strategies to conduct feasibilities in the UK and Hungary. The position may suit 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, 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 the assigned country.
- Conduct/expedite 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.
- 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.
- 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 and prep/consultation support for site audits.
- Minimum a Bachelor of Science in a health-related field.
- Minimum 1 year of site and clinical trials experience (more experience for more senior roles).
- CRA experience is an asset.
- Knowledge of drug development, clinical trial management and operational procedures, including GCP guidelines, is preferred.
- Knowledge of medical terminology and clinical patient management is preferred.
- Fluency in English; Finnish is a plus.
- Demonstrated organizational and prioritization skills.
- Excellent oral and written communication skills.
- Proficient knowledge of Microsoft Office applications.
At Medpace, you will find work that is both challenging and rewarding. You will be given the tools and training to succeed, and you will be rewarded for strong performance with opportunities to grow professionally.
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 a scientific and disciplined approach.
Flexible work environment, competitive compensation and benefits package, competitive PTO packages, structured career paths with opportunities for professional growth, company-sponsored employee appreciation events, and employee health and wellness initiatives.
Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024.
Clinical Trial Site Relationship Coordinator (Finnish Speaking) in London employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Site Relationship Coordinator (Finnish Speaking) in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who might know about opportunities at Medpace. A friendly chat can sometimes lead to a referral, which is golden in landing that job.
✨Tip Number 2
Prepare for interviews by researching Medpace and its projects. Knowing the ins and outs of their clinical trials and recent developments will show you're genuinely interested and ready to contribute from day one.
✨Tip Number 3
Practice your communication skills! As a Clinical Trial Site Relationship Coordinator, you'll need to build relationships and communicate effectively. Role-play with a friend or use online resources to sharpen those skills.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re serious about joining the Medpace team!
We think you need these skills to ace Clinical Trial Site Relationship Coordinator (Finnish 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 any relevant clinical research experience and skills that match the job description. We want to see how your background aligns 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 passionate about this role and how your experience makes you a great fit. Don’t forget to mention your fluency in Finnish if applicable, as it’s a plus for us!
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 before hitting send!
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 to do!
How to prepare for a job interview at Medpace
✨Know Your Clinical Research Basics
Make sure you brush up on your knowledge of clinical trials, GCP guidelines, and drug development processes. Being able to discuss these topics confidently will show that you understand the industry and can contribute effectively.
✨Showcase Your Relationship-Building Skills
Since this role involves maintaining strategic relationships with sites, prepare examples of how you've successfully built and managed relationships in previous roles. Highlight your communication skills and any relevant experiences that demonstrate your ability to connect with stakeholders.
✨Research the Company and Its Studies
Take some time to learn about Medpace and their recent studies or projects. Understanding their mission and values will help you align your answers with what they’re looking for, and it shows genuine interest in the company.
✨Prepare Questions for Your Interviewers
Think of insightful questions to ask during your interview. This could be about their site selection process or how they handle feasibility assessments. Asking thoughtful questions not only demonstrates your interest but also gives you a chance to assess if the company is the right fit for you.