At a Glance
- Tasks: Join a team conducting vital research for drug and medical device development.
- Company: Medpace, a leading clinical contract research organisation with a mission to improve lives.
- Benefits: Flexible work environment, competitive pay, and structured career growth opportunities.
- Other info: Dynamic role with travel opportunities and a chance to impact patient lives.
- Why this job: Make a real difference in healthcare while exploring the UK and gaining valuable experience.
- Qualifications: Bachelor's degree in health or life sciences preferred; strong communication skills are a plus.
The predicted salary is between 28800 - 48000 £ per year.
The Clinical Research Associate at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them.
For those with medical and/or health/life science interest and background who want to explore the research field, travel the UK, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you.
Please note that to take full advantage of the training on offer, you must be within commuting distance of our Medpace central London office.
Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields. Individuals who have succeeded in the CRA role include:
- Nurses
- Dieticians
- Pharmacy Technicians
- Pharmaceutical/Device Sales Representatives
- Biotech Engineers
- PhD/Pharm.D candidates
- Health and Wellness Coordinators
- Site Coordinators, Clinical Research Coordinators
- Research Assistants
Responsibilities
- Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
- Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
- Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
- Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
- Verification that the investigator is enrolling only eligible subjects;
- Regulatory document review;
- Medical device and/or investigational product/drug accountability and inventory;
- Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
- Assessing the clinical research site's patient recruitment and retention success and offering suggestions for improvement;
- Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.
Qualifications
- Minimum of a bachelor's degree; Health or life science related field preferred;
- Willing to travel approximately *****% nationally;
- Familiarity with Microsoft Office;
- Strong communication and presentation skills a plus;
- Must hold a valid drivers licence.
Medpace Overview
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 its scientific and disciplined approach.
Why Medpace?
People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today. The work we've done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.
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
Awards
Recognized by Forbes as one of America's Most Successful Midsize Companies in ****, ****, **** and ****. Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
EO/AA Employer M/F/Disability/Vets
Entry Level in England employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Entry Level in England
✨Tip Number 1
Network like a pro! Reach out to your connections in the medical and life sciences fields. Attend industry events or webinars, and don’t be shy about introducing yourself. You never know who might have a lead on that perfect entry-level position!
✨Tip Number 2
Prepare for interviews by researching Medpace and its mission. Understand their work in clinical research and think about how your background fits into their goals. This will help you stand out and show that you're genuinely interested in making a difference.
✨Tip Number 3
Practice your communication skills! As a Clinical Research Associate, you'll need to interact with various stakeholders. Role-play common interview questions with friends or family to boost your confidence and refine your responses.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, it shows you’re serious about joining the Medpace team. So, get those applications in and let’s make a difference together!
We think you need these skills to ace Entry Level in England
Some tips for your application 🫡
Tailor Your CV: Make sure your CV reflects the skills and experiences that align with the Clinical Research Associate role. Highlight any relevant medical or life science background, and don’t forget to mention your communication skills!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to express your passion for clinical research and how you can contribute to Medpace's mission. Be genuine and let your personality come through.
Showcase Your Attention to Detail: As a CRA, attention to detail is key. In your application, make sure there are no typos or errors. This shows us that you take pride in your work and understand the importance of accuracy in clinical research.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and allows us to see your enthusiasm for joining the Medpace team!
How to prepare for a job interview at Medpace
✨Know Your Stuff
Make sure you brush up on your knowledge of clinical research and the specific responsibilities of a Clinical Research Associate. Familiarise yourself with terms like GCP, SOPs, and the drug development process. This will show that you're genuinely interested in the role and understand what it entails.
✨Showcase Your Background
Since Medpace values varied backgrounds, be ready to discuss how your previous experiences—whether as a nurse, dietician, or in any related field—have prepared you for this role. Highlight specific skills or situations where you demonstrated strong communication or problem-solving abilities.
✨Prepare Questions
Interviews are a two-way street! Prepare thoughtful questions about the company culture, team dynamics, and the training opportunities available. This not only shows your enthusiasm but also helps you gauge if Medpace is the right fit for you.
✨Practice Makes Perfect
Conduct mock interviews with friends or family to practice your responses. Focus on articulating your thoughts clearly and confidently. The more comfortable you are speaking about your experiences and aspirations, the better you'll perform during the actual interview.