At a Glance
- Tasks: Conduct research visits and ensure compliance in drug and medical device studies.
- Company: Join Medpace, a leading clinical research organisation making a real difference.
- Benefits: Flexible work environment, competitive pay, and structured career growth opportunities.
- Why this job: Travel the UK while contributing to life-changing medical advancements.
- Qualifications: Bachelor's degree in health or life sciences; strong communication skills preferred.
- Other info: Dynamic role with mentorship and potential for management advancement.
The predicted salary is between 28800 - 48000 £ per year.
Overview
The Clinical Research Associate at Medpace offers an exciting career in the research of drug and medical device development while making a difference in the lives of patients. 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. Please note that to take full advantage of the training on offer, you must be within commuting distance of our Medpace central London office as this role is initially fully office based.
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
- Dietitians
- Pharmacy Technicians
- Pharmaceutical/Device Sales Representatives
- Biotech Engineers
- PhD/Pharm.D candidates
- Health and Wellness Coordinators
- Site Coordinators, Clinical Research Coordinators
- Research Assistants
PACE – MEDPACE CRA TRAINING PROGRAM
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 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.
UNEXPECTED REWARDS
This role involves travel and excitement and offers the opportunity to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices. The CRA position provides additional advantages including:
- Dynamic working environment with varying day-to-day responsibilities
- 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 bonus program
Responsibilities
- Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol
- Communicate with site staff including coordinators, clinical research physicians, and their site staff
- Verify adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff
- Verify medical record and research source documentation against case report data; inform site staff of entry errors, ensure good documentation practices, and communicate protocol deviations per SOPs, GCP and applicable regulatory requirements
- Verify that the investigator is enrolling only eligible subjects
- Regulatory document review
- Medical device and/or investigational product/drug accountability and inventory
- Verify and review adverse events, serious adverse events, concomitant medications and illnesses to confirm accurate data reporting per the protocol
- Assess the site’s patient recruitment and retention success and offer improvement suggestions
- Complete monitoring reports and follow-up letters with summaries of 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 are a plus
- Must hold a valid driver’s licence
- Willing to be fully office based during the core training program
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 a scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs more than 5,000 people across 40+ countries.
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 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
What to Expect Next
A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.
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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 like a pro! Reach out to professionals in the clinical research field on LinkedIn or at local events. We can’t stress enough how valuable personal connections can be in landing that entry-level CRA role.
✨Tip Number 2
Prepare for interviews by practising common CRA questions and scenarios. We recommend doing mock interviews with friends or mentors to boost your confidence and refine your answers.
✨Tip Number 3
Show your passion for clinical research! During interviews, share your enthusiasm for making a difference in patients' lives and how your background aligns with the CRA role. We want to see that spark!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take the initiative to connect directly with us.
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 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 any experience with research or clinical settings!
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 sure to mention why you're excited about the opportunity and how your background fits the bill.
Showcase Your Communication Skills: As a CRA, communication is key! In your application, demonstrate your strong communication abilities. Whether it's through your writing style or by mentioning past experiences where you effectively communicated with teams or patients, make it clear that you can convey information clearly.
Apply Through Our Website: We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status. Plus, we love seeing applications come in through our own platform!
How to prepare for a job interview at Medpace
✨Know Your Stuff
Make sure you brush up on the basics of clinical research and the specific responsibilities of a Clinical Research Associate. Familiarise yourself with terms like GCP (Good Clinical Practice) and the drug development process, as this will show your genuine interest in the role.
✨Showcase Your Background
Since candidates from various health and life science backgrounds are welcome, be ready to discuss how your unique experiences—whether as a nurse, dietitian, or even a pharmacy technician—can contribute to the CRA role. Highlight any relevant skills or knowledge that align with the job description.
✨Prepare Questions
Interviews are a two-way street! Prepare thoughtful questions about the PACE Training Program and what a typical day looks like for a CRA at Medpace. This not only shows your enthusiasm but also helps you gauge if the company is the right fit for you.
✨Practice Your Communication Skills
Strong communication is key in this role, so practice articulating your thoughts clearly and confidently. You might want to do mock interviews with friends or family to get comfortable discussing your qualifications and experiences.