At a Glance
- Tasks: Lead clinical trials with medical expertise and strategic oversight.
- Company: Join Medpace, a global leader in clinical research with over 5,000 employees.
- Benefits: Enjoy hybrid work flexibility, competitive pay, and generous PTO.
- Why this job: Make a real impact on patients' lives while growing your career in a supportive environment.
- Qualifications: Must hold an M.D. in CNS/neuro, with board certification and clinical trial experience preferred.
- Other info: Travel up to 20% may be required.
The predicted salary is between 43200 - 72000 Β£ per year.
Overview
We are seeking a CNS Medical Monitor 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.
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., specialization in CNS / neurology and current medical licensure;
- Board certification;
- Prior clinical trial research experience preferred;
- Previous experience in pharmaceutical-related clinical research is preferred.
Travel: up to 20%
About Medpace
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.
Awards
- Recognized by Forbes as one of America\\\βs 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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Medical Monitor - CNS employer: Medpace
Contact Detail:
Medpace Recruiting Team
StudySmarter Expert Advice π€«
We think this is how you could land Medical Monitor - CNS
β¨Tip Number 1
Network with professionals in the CNS field. Attend relevant conferences or webinars where you can meet current Medical Monitors or those working in clinical trials. This can provide you with insights into the role and potentially lead to referrals.
β¨Tip Number 2
Stay updated on the latest developments in CNS research and clinical trials. Subscribe to industry journals or follow key opinion leaders on social media. This knowledge will not only enhance your expertise but also demonstrate your commitment during interviews.
β¨Tip Number 3
Prepare to discuss your previous clinical trial experiences in detail. Be ready to explain how you've managed safety issues or contributed to study reports, as these are crucial aspects of the Medical Monitor role.
β¨Tip Number 4
Familiarise yourself with Medpace's mission and values. Understanding their approach to clinical trials and patient care will help you align your answers with their goals during the interview process.
We think you need these skills to ace Medical Monitor - CNS
Some tips for your application π«‘
Tailor Your CV: Make sure your CV highlights your M.D. qualification, CNS/neuro-specialisation, and any relevant clinical trial experience. Use specific examples to demonstrate your expertise in medical management and leadership in clinical trials.
Craft a Compelling Cover Letter: In your cover letter, express your passion for clinical research and how your background aligns with the responsibilities of the Medical Monitor role. Mention your experience with study design and protocol development, as well as your ability to manage safety issues.
Highlight Relevant Experience: When detailing your previous roles, focus on your contributions to clinical trials, including any involvement in regulatory documents or manuscripts. Emphasise your collaborative work with other departments and your adherence to research protocols.
Showcase Your Certifications: Include your board certification and current medical licensure prominently in your application. This is crucial for establishing your credibility as a candidate for the Medical Monitor position.
How to prepare for a job interview at Medpace
β¨Showcase Your Medical Expertise
As a Medical Monitor, your medical knowledge is crucial. Be prepared to discuss your experience in CNS and neurology, highlighting specific cases or trials you've worked on. This will demonstrate your capability to provide the necessary medical leadership.
β¨Familiarise Yourself with Clinical Trials
Understand the clinical trial process thoroughly. Be ready to talk about your previous experiences managing safety issues and how you contributed to study reports. This shows that you can handle the responsibilities of the role effectively.
β¨Prepare for Interdepartmental Coordination
Since the role involves working with various departments, think of examples where you've successfully collaborated with others. Discuss how you managed communication and coordination during trials, as this will highlight your teamwork skills.
β¨Demonstrate Your Passion for Patient Impact
Medpace values making a difference in patients' lives. Share your motivation for working in clinical research and how your contributions can lead to better therapeutic outcomes. This will resonate well with the company's mission and values.