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- Tasks: Join our team to conduct vital clinical research and support drug development.
- Company: Medpace is a leading clinical research organisation dedicated to advancing medical therapeutics.
- Benefits: Enjoy hybrid work options, competitive PTO, wellness initiatives, and structured career paths.
- Why this job: Make a real impact on patients' lives while growing your career in a dynamic environment.
- Qualifications: Bachelor's in health-related field and 2+ years of monitoring experience required.
- Other info: Recognised by Forbes as one of America's Best Mid-size Companies for four consecutive years.
The predicted salary is between 28800 - 48000 £ per year.
Our clinical activities are growing rapidly, and we are currently seeking full-time, home or office-based Clinical Research Associates to join our Clinical Monitoring team in the UK. This position will work with a team to accomplish tasks and projects that are instrumental to the company\’s success. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.
The Clinical Research Associate at Medpace is offered the unique opportunity to be involved at every stage of the drug development process by providing unrivalled support to our customers. If you want an exciting career where you use your medical or health background and education, travel extensively and are instrumental in the clinical trials process, this could be the opportunity for you. Our successful Clinical Research Associates possess varied backgrounds in the medical and related healthcare fields. Individuals who have succeeded in the CRA role include Registered Nurses, Dieticians, Pharmacists, Faculty of Science Graduates and Research Assistants. An extensive training program provides the platform to effectively and confidently carry out your duties.
Responsibilities
- Conduct pre-study, initiation, monitoring, and closeout visits for research sites;
- Perform source document verification and case report form review;
- Perform regulatory document review;
- Conduct study drug inventory;
- Perform adverse event and serious adverse event reporting and follow-up; and
- Assess patient recruitment and retention.
Qualifications
- Minimum of a bachelor of science in health-related field, MD or equivalent;
- 2+ years of independent monitoring experience;
- Broad knowledge of medical terminology and clinical patient management;
- Basic knowledge of drug therapy techniques and clinical research methodologies;
- Fluency in English
- 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. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing 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 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
- Hybrid work-from-home options (dependent upon position and level)
- Competitive PTO packages
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
- Flexible work schedule
- Competitive compensation and benefits package
- Structured career paths with opportunities for professional growth
Awards
- Recognized by Forbes as one of America\’s Best Mid-size 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.
EO/AA Employer M/F/Disability/Vets #J-18808-Ljbffr
Experienced Clinical Research Associate (CRA) (home and office based positions available) employer: Medpace, Inc.
Contact Detail:
Medpace, Inc. Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Experienced Clinical Research Associate (CRA) (home and office based positions available)
✨Tip Number 1
Network with professionals in the clinical research field. Attend industry conferences, webinars, or local meetups to connect with current Clinical Research Associates and learn about their experiences at Medpace.
✨Tip Number 2
Familiarise yourself with Medpace's specific therapeutic areas and recent projects. This knowledge will help you demonstrate your genuine interest in the company during any interviews or discussions.
✨Tip Number 3
Prepare for potential interview questions by reviewing common scenarios faced by Clinical Research Associates. Think about how your previous experience aligns with the responsibilities outlined in the job description.
✨Tip Number 4
Showcase your adaptability and willingness to learn. Highlight any relevant training or certifications you've completed that demonstrate your commitment to staying updated in the clinical research field.
We think you need these skills to ace Experienced Clinical Research Associate (CRA) (home and office based positions available)
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical research, particularly any independent monitoring roles. Emphasise your medical or health background and any specific skills that align with the job description.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for clinical research and your understanding of the drug development process. Mention how your previous experiences make you a great fit for the Clinical Research Associate role at Medpace.
Highlight Relevant Qualifications: Clearly state your qualifications, including your degree in a health-related field and any certifications. If you have experience with regulatory document review or patient management, be sure to include that as well.
Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial in clinical research.
How to prepare for a job interview at Medpace, Inc.
✨Know Your Clinical Research Basics
Brush up on your knowledge of clinical research methodologies and drug therapy techniques. Be prepared to discuss how your background in the medical field can contribute to the role, as this will show your understanding of the industry.
✨Demonstrate Your Monitoring Experience
Highlight your independent monitoring experience during the interview. Be ready to share specific examples of past projects or studies you've worked on, focusing on your role and the outcomes achieved.
✨Showcase Your Communication Skills
As a Clinical Research Associate, effective communication is key. Prepare to discuss how you have successfully communicated with various stakeholders, including research sites and team members, to ensure smooth project execution.
✨Ask Insightful Questions
Prepare thoughtful questions about the company's clinical activities and future projects. This not only shows your interest in the position but also demonstrates your proactive approach to understanding the role and its impact on the company.
