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For Companies At a Glance
- Tasks: Lead clinical trials with medical expertise and strategic oversight.
- Company: Join Medpace, a leading clinical research organisation making a global impact.
- Benefits: Enjoy flexible work, competitive pay, and career growth opportunities.
- Why this job: Make a real difference in patients' lives through innovative medical research.
- Qualifications: M.D. degree required; clinical trial experience preferred.
- Other info: Hybrid work model with travel up to 20%.
The predicted salary is between 36000 - 60000 £ per year.
We are seeking several Medical Monitors to join our dynamic team. The Medical Monitor will have overall responsibility for providing medical, scientific, and strategic leadership for the successful planning, execution, and reporting of clinical trials. Additionally, this role acts as the Medpace internal medical expert and will serve as a medical resource for the review, presentation, and interpretation of results in the Clinical Study Report. The Medical Monitor will also be involved in the development of new clinical projects, including study design, protocol, and project plans as required.
We are currently seeking Medical Monitors in the following Therapeutic Areas:
- Psychiatry
- Pediatric / Neuromuscular Neurology
- Oncology (solid tumor)
- Hepatology
- Dermatology
- Metabolic / Endocrinology
All Medical Monitors have hybrid WFH flexibility.
Responsibilities
- Provide medical management and expertise for clinical trials;
- Contribute medical expertise to study reports, regulatory documents, and manuscripts;
- Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;
- Participate in new business development through involvement in proposal and sponsor meetings as requested;
- Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;
- Follow specific research related protocol and lead others in strict adherence to the policies.
Qualifications
- Must have an M.D. degree or equivalent. Board certification and current medical licensure are preferred;
- Must have prior clinical trial research experience;
- Previous experience in pharmaceutical-related clinical research is preferred.
Travel: up to 20%
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
- 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.
Medical Monitor employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Medical Monitor
✨Network Like a Pro
Get out there and connect with people in the industry! Attend conferences, webinars, or local meetups related to clinical trials. You never know who might have a lead on your dream Medical Monitor role.
✨Show Off Your Expertise
When you get the chance to chat with potential employers, don’t hold back! Share your insights on clinical trials and your experience in the therapeutic areas they’re focused on. This will show them you’re not just another candidate, but a valuable asset.
✨Ace the Interview
Prepare for your interviews by researching common questions for Medical Monitors and practising your responses. Be ready to discuss your previous clinical trial experiences and how you can contribute to their projects. Confidence is key!
✨Apply Through Our Website
Don’t forget to apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining our team at Medpace.
We think you need these skills to ace Medical Monitor
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Medical Monitor role. Highlight your relevant experience in clinical trials and any specific therapeutic areas you’ve worked in. We want to see how your background aligns with what we’re looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about this role and how your skills can contribute to our mission at Medpace. Keep it concise but impactful – we love a good story!
Showcase Your Medical Expertise: Since the Medical Monitor role requires medical management and expertise, be sure to highlight your qualifications, such as your M.D. degree and any board certifications. We’re looking for candidates who can bring their medical knowledge to the table!
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. Plus, you’ll find all the details about the role and our company culture there!
How to prepare for a job interview at Medpace
✨Know Your Therapeutic Areas
Familiarise yourself with the specific therapeutic areas mentioned in the job description, such as Psychiatry and Oncology. Be prepared to discuss your experience and insights related to these fields, as this will demonstrate your expertise and alignment with the role.
✨Showcase Your Clinical Trial Experience
Highlight your previous clinical trial research experience during the interview. Prepare examples of how you've contributed to study design, protocol development, or safety management in past roles. This will help the interviewers see your practical knowledge and how it applies to their needs.
✨Prepare for Medical Management Scenarios
Anticipate questions about managing safety issues in clinical trials. Think through potential scenarios you might face and how you would handle them. This shows that you can think critically and act decisively, which is crucial for a Medical Monitor.
✨Engage with the Company’s Mission
Understand Medpace's mission to accelerate the development of medical therapeutics. Be ready to discuss how your values align with theirs and how you can contribute to making a difference in patients' lives. This connection can set you apart from other candidates.
