​Medical Director - Clinical Development

Location Cincinnati
Discipline: Medical & Pharmacovigilance
Job type: Permanent
Salary: £Salary: $325,000 - $350,000 Per annum + 30% bonus and stock
Contact name: Stuart Gilboy

Contact email: stuart.gilboy@rbwconsulting.com
Contact phone: 16179821238
Job ref: 21407
Published: 4 days ago
Expiry date: 06 May 2021

Location: Cincinnati, Ohio

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. They leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

This is an award winning multi-national CRO which provides an ideal entry point into the pharmaceutical industry for physicians with clinical research experience. You will move from shifts and on call to office hours with deadlines, but which are managed well. This can be a lucrative venture as excellent bonuses are paid, and stock grants are offered.

Job Summary

They are seeking a Medical Director to join a 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 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. They are currently seeking Medical Directors in the following Therapeutic Areas:

  • Cardiology (adult)

  • Gastroenterology

  • Endocrinology

  • Radiology

  • Infectious Disease

  • Immunology

  • Safety

  • Nephrology

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. with board certification and current medical licensure;

  • Must have prior clinical trial research experience; and

  • Previous experience in pharmaceutical-related clinical research is preferred.

You will become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Their employees provide hope for those living with debilitating diseases. They invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.

For more information on this role please forward an up to date resume to stuart.gilboy@rbwconsulting.com

Salary: $325,000 - $350,000 Per annum + 30% bonus and stock