Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Join us as a Clinical Research Associate, conducting site visits and ensuring compliance in drug research.
- Company: Medpace is a leading clinical research organisation dedicated to advancing medical therapeutics globally.
- Benefits: Enjoy flexible work, competitive pay, travel bonuses, and structured career growth opportunities.
- Why this job: Make a real impact in healthcare while travelling the UK and working with experts in the field.
- Qualifications: A bachelor's degree in health or life sciences is preferred; strong communication skills are a plus.
- Other info: Must be within commuting distance of our London office and willing to travel 60-80% nationally.
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 pharmaceuticals 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
Through our PACE® Training Program, you will join other Professionals Achieving CRA Excellence: PACE® provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA. PACE® will prepare you by developing your CRA skills through interactive discussions and hands-on job-related exercises and practicums. To supplement your in-house and field-based training, you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.
This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides many other distinctive advantages including:
- Dynamic working environment, with varying responsibilities day-to-day
- Expansive experience in multiple therapeutic areas
- Work within a team of therapeutic and regulatory experts
- Defined CRA promotion and growth ladder with potential for mentoring and management advancements
- Competitive pay and opportunity for significant travel bonus
Responsibilities include:
- 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
- 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 60-80% nationally
- Familiarity with Microsoft® Office
- Strong communication and presentation skills a plus
- Must hold a valid driver’s licence
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 2021, 2022, 2023 and 2024. Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
Entry Level - Clinical Research Associate employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Entry Level - Clinical Research Associate
✨Tip Number 1
Network with professionals in the clinical research field. Attend industry events, webinars, or local meetups to connect with current Clinical Research Associates and learn about their experiences. This can provide valuable insights and potentially lead to referrals.
✨Tip Number 2
Familiarise yourself with the latest trends and regulations in clinical research. Keeping up-to-date with industry news will not only enhance your knowledge but also demonstrate your commitment to the field during interviews.
✨Tip Number 3
Consider shadowing a Clinical Research Associate or volunteering at a clinical site. Gaining hands-on experience, even if it's informal, can give you a better understanding of the role and make you a more attractive candidate.
✨Tip Number 4
Prepare for potential interview questions by practising your responses to common scenarios faced by Clinical Research Associates. Think about how your background in health or life sciences can be applied to the responsibilities outlined in the job description.
We think you need these skills to ace Entry Level - Clinical Research Associate
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in medical or health/life sciences. Emphasise any roles that involved research, patient interaction, or teamwork, as these are crucial for the Clinical Research Associate position.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the role. Mention specific experiences that align with the responsibilities outlined in the job description, such as monitoring or data verification.
Highlight Relevant Skills: In your application, emphasise skills that are particularly relevant to the role, such as strong communication abilities, attention to detail, and familiarity with Microsoft Office. These will help demonstrate your suitability for the position.
Proofread Your Application: Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects your professionalism and attention to detail, which are essential traits for a Clinical Research Associate.
How to prepare for a job interview at Medpace
✨Know Your Background
Make sure you can clearly articulate your educational background and any relevant experience in health or life sciences. Highlight how your previous roles, whether as a nurse, dietician, or research assistant, have prepared you for the Clinical Research Associate position.
✨Understand the Role
Familiarise yourself with the responsibilities of a Clinical Research Associate. Be ready to discuss how you would conduct monitoring visits, verify documentation, and ensure compliance with protocols. Showing that you understand the nuances of the role will impress your interviewers.
✨Demonstrate Communication Skills
Since strong communication is key in this role, prepare examples of how you've effectively communicated with team members or site staff in the past. This could include resolving issues, providing feedback, or collaborating on projects.
✨Show Enthusiasm for Travel
The job involves significant travel, so express your excitement about the opportunity to visit different sites across the UK. Share any previous experiences that demonstrate your adaptability and willingness to travel for work.
