Hepatologist/GI specialist - Medical Director
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Hepatologist/GI specialist - Medical Director

Hepatologist/GI specialist - Medical Director

London Full-Time 72000 - 108000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead clinical trials and provide medical expertise in a dynamic team environment.
  • Company: Medpace is a global leader in clinical research, impacting lives through innovative medical solutions.
  • Benefits: Enjoy flexible work options, competitive pay, and structured career growth opportunities.
  • Why this job: Make a real difference in patients' lives while working on cutting-edge medical projects.
  • Qualifications: Must have an M.D. in Hepatology/GI with board certification and clinical trial experience.
  • Other info: Hybrid work flexibility available; travel up to 20% required.

The predicted salary is between 72000 - 108000 £ per year.

Job Summary: We are seeking a Hepatologist/GI specialist – Medical Director to join our dynamic team. The Medical Director 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 Director 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 Directors in different locations. All Medical Directors have hybrid WFH flexibility. This role also has the ability to be fully remote with the right experience. 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 Hepatology/GI 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% 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: 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. EO/AA Employer M/F/Disability/Vets #J-18808-Ljbffr

Hepatologist/GI specialist - Medical Director employer: Medpace, Inc.

At Medpace, we pride ourselves on being an exceptional employer, offering a flexible work environment that supports both hybrid and fully remote options for our Medical Directors. Our commitment to employee growth is evident through structured career paths and professional development opportunities, all while fostering a culture of collaboration and innovation. Join us in making a meaningful impact on global health, backed by competitive compensation, comprehensive benefits, and a strong focus on employee wellness.
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Contact Detail:

Medpace, Inc. Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Hepatologist/GI specialist - Medical Director

✨Tip Number 1

Make sure to highlight your clinical trial research experience during the interview. Discuss specific trials you've worked on and how your expertise in Hepatology/GI contributed to their success.

✨Tip Number 2

Familiarize yourself with Medpace's mission and values. Be prepared to discuss how your personal goals align with their commitment to improving patient lives through clinical research.

✨Tip Number 3

Network with current or former Medpace employees on platforms like LinkedIn. They can provide insights into the company culture and what it takes to succeed as a Medical Director.

✨Tip Number 4

Prepare to discuss your approach to managing safety issues in clinical trials. Share examples of how you've effectively handled challenges in past projects to demonstrate your leadership skills.

We think you need these skills to ace Hepatologist/GI specialist - Medical Director

Medical Expertise in Hepatology/GI
Clinical Trial Management
Regulatory Knowledge
Study Design and Protocol Development
Data Interpretation and Reporting
Safety Assessment in Clinical Trials
Collaboration with Cross-Functional Teams
Proposal Development
Strong Communication Skills
Leadership and Team Management
Attention to Detail
Problem-Solving Skills
Adaptability to Hybrid Work Environment
Experience in Pharmaceutical Clinical Research

Some tips for your application 🫡

Understand the Role: Make sure you fully understand the responsibilities and qualifications required for the Hepatologist/GI specialist - Medical Director position. Tailor your application to highlight relevant experience in clinical trials and medical management.

Highlight Relevant Experience: In your CV and cover letter, emphasize your M.D. degree, specialization in Hepatology/GI, and any prior clinical trial research experience. Mention specific projects or roles that demonstrate your expertise in medical leadership and strategic planning.

Craft a Strong Cover Letter: Write a compelling cover letter that outlines your passion for clinical research and how your background aligns with Medpace's mission. Discuss your ability to manage safety issues in clinical trials and your experience in developing study protocols.

Review and Edit: Before submitting your application, thoroughly review all documents for clarity and accuracy. Ensure that your application is free of errors and clearly communicates your qualifications and enthusiasm for the role.

How to prepare for a job interview at Medpace, Inc.

✨Showcase Your Medical Expertise

As a Hepatologist/GI specialist, it's crucial to demonstrate your deep understanding of the field. Be prepared to discuss your clinical trial experience and how it relates to the responsibilities of the Medical Director role.

✨Discuss Your Leadership Experience

Highlight any previous roles where you provided medical, scientific, or strategic leadership. Share specific examples of how you've successfully managed teams or projects in clinical trials.

✨Prepare for Regulatory Discussions

Since the role involves contributing to regulatory documents and study reports, familiarize yourself with relevant regulations and guidelines. Be ready to discuss how you've navigated these in past projects.

✨Emphasize Collaboration Skills

The position requires coordination with various departments. Prepare examples that showcase your ability to work collaboratively across teams, especially in the context of clinical studies and trials.

Hepatologist/GI specialist - Medical Director
Medpace, Inc.
Apply now
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