At a Glance
- Tasks: Coordinate clinical trial sites and build strategic relationships for innovative 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: Be part of a supportive environment with employee wellness initiatives.
- Why this job: Make a real impact in drug development while reducing travel.
- Qualifications: Bachelor's in health-related field and clinical trials experience 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.
- 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.
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 and Finnish.
- 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 (Finnish 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 (Finnish Speaking)
✨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 when it comes to landing that job.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Show us you’re genuinely interested in what we do! Think about how your skills can contribute to our mission of delivering innovative research and development.
✨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 your skills before the big day.
✨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 us you’re serious about joining our vibrant team!
We think you need these skills to ace Clinical Trial Site Relationship Coordinator (Finnish 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 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 a great fit. Don’t forget to mention your fluency in Finnish – it’s a big plus for us!
Showcase Your Communication Skills:Since this role involves building relationships, make sure your written application reflects your excellent communication skills. Keep it clear, concise, and professional, but let your personality shine through too!
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!
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 strategies you used to keep those connections strong, as this will demonstrate your capability in this area.
✨Prepare for Site-Specific Questions
Research the site landscape in the UK and Hungary, including key opinion leaders and site capabilities. This knowledge will help you answer questions about how you would approach feasibility assessments and site selection, making you stand out as a candidate who’s proactive and well-prepared.
✨Practice Your Communication Skills
As excellent communication is key for this role, practice articulating your thoughts clearly and concisely. You might even want to do a mock interview with a friend to get comfortable discussing your experiences and answering potential questions in a confident manner.
