Medical Director, Neurologist

IQVIA•Durham, NC

13d•Remote

About The Position

Medical Director, Neurologist Job Overview The Medical Director will be the medical expert on the IQVIA team working on a clinical research trial. This involves applying medical and scientific knowledge and expertise in support of the trial. These clinical trials will cover the full range of neurologic disorders. Essential Functions The role includes predominantly Medical Monitoring responsibilities with Medical Strategic input involvement as requested. Medical Monitoring: Primarily serves as Medical Monitor (at the global or regional level) on assigned clinical trials. Serves as Scientific Advisor (providing medical advice and input) to Project Leaders on the medical and scientific aspects of assigned projects. Provides medical support to investigative sites and project staff for protocol-related issues including Provides therapeutic area/indication training for the project clinical team. Attends and presents at Investigator Meetings. Performs review and clarification of trial-related Adverse Events (AEs). Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested. Available to respond to urgent protocol-related issues at the investigative sites. Medical Strategy: Contributes to the development of the medically related aspects of client proposals including the budget related to medical monitoring. Provides medical and scientific advice and guidance to key internal stakeholders developing proposals: this may include reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape. Attends and presents at bid defense meetings, as required. Requires 5% periodic regional and international travel. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe The potential base pay range for this role, when annualized, is $154,900.00 - $431,500.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. To get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us.

Requirements

Medical degree from an accredited and internationally recognized medical school
Board certified or eligible in Neurology
Ideally, candidate will have a minimum 2 years clinical trials experience as an investigator or medical /clinical expert in the Pharma, CRO, or Biotech industry.
Ability to establish and maintain effective working relationships with coworkers, managers and clients.
Strong communication, presentation and interpersonal skills, including good command of English language (both written and spoken).
Robust and current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in Neurology.
Proven skills in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility.
Availability for intermittent domestic and foreign travel to support these business assignments.

Nice To Haves

Subspecialty interest and training in neuromuscular diseases (ALS, myasthenia gravis, neuropathy), or sleep disorders, or pediatric neurology is a plus, but not required. In fact, the assigned clinical trials will cover the full range of neurologic disorders.

Responsibilities

Primarily serves as Medical Monitor (at the global or regional level) on assigned clinical trials.
Serves as Scientific Advisor (providing medical advice and input) to Project Leaders on the medical and scientific aspects of assigned projects.
Provides medical support to investigative sites and project staff for protocol-related issues including Provides therapeutic area/indication training for the project clinical team.
Attends and presents at Investigator Meetings.
Performs review and clarification of trial-related Adverse Events (AEs).
Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
Available to respond to urgent protocol-related issues at the investigative sites.
Contributes to the development of the medically related aspects of client proposals including the budget related to medical monitoring.
Provides medical and scientific advice and guidance to key internal stakeholders developing proposals: this may include reviewing the protocol for scientific/regulatory soundness and feasibility, identification of target site and principal investigator profiles, anticipated patient recruitment, standard of care and competitive landscape.
Attends and presents at bid defense meetings, as required.