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IQVIA

Runs drug trials and sells health data to pharma

Medical Director - Gastroenterology

Biology & BiotechConfirmed live in the last 24 hours
Full-timeDurham, NC, USA

About the Job

Requirements

  • Be available 24 hours per day, 7 days per week, to respond to urgent protocol-related issues at investigative sites.
  • May require regular travel.
  • Use a keyboard extensively, requiring repetitive motion of the fingers.
  • Use the telephone and face-to-face communication extensively, requiring accurate perception of speech.
  • Have excellent communication, presentation, and interpersonal skills, including command of written and spoken English.
  • Hold a medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
  • Hold mandatory Gastroenterology certification; specialty board certification is required.
  • Have at least 5 years of experience in clinical medicine in addition to 4 years of clinical trials experience as an investigator or in the pharmaceutical, contract research organization, or biotechnology industry.
  • Have robust and current knowledge of the scientific, clinical, regulatory, commercial, and competitive landscape in the applicable therapeutic area.
  • Know applicable federal and local regulations and guidelines pertaining to clinical research.
  • Have skills providing consultation and advice on multiple assignments, as well as initiative and flexibility.

Responsibilities

  • Serve primarily as Global Medical Advisor on assigned projects.
  • Serve as Scientific Advisor and guide Project Leaders on the medical and scientific aspects of assigned projects.
  • Provide medical support to investigative sites and project staff on protocol-related issues, including protocol clarifications, inclusion and exclusion determinations, and patient safety or eligibility issues.
  • Review medical aspects of protocols, Investigative Drug Brochures, and Case Report Forms.
  • Review and clarify trial-related adverse events.
  • Provide therapeutic area and indication training for the project clinical team.
  • Attend and present at Investigator Meetings.
  • May conduct medical case reviews of Serious Adverse Events, including case documentation and patient narratives, in collaboration with Pharmacovigilance.
  • May provide medical support for Analysis of Similar Events in collaboration with or on behalf of Pharmacovigilance.
  • May review adverse event coding medically.
  • Review Clinical Study Reports and patient narratives.
  • Attend Kick-Off meetings, weekly team meetings, and client meetings as needed or requested.
  • Provide medical, clinical, and scientific advisory expertise to IQVIA divisions as requested.
  • Participate in all aspects of Medical Science involvement on assigned trials.
  • Serve as a medical expert during the project delivery lifecycle.
  • Provide therapeutic and medical expertise to business development activities.

About the Company

IQVIA

Runs drug trials and sells health data to pharma

IQVIA runs clinical trials for drug, biotech and medical device companies and sells them the health data, software and analytics they use to develop and market treatments. Its research arm designs studies, recruits trial sites and patients, and manages trials through to regulatory filing. Its commercial arm sells market data, consulting and software that pharma sales and marketing teams use to plan product launches. Clients pay through multi-year service contracts and data and software subscriptions. IQVIA was formed in 2016 when clinical research firm Quintiles merged with health data company IMS Health, and it is based in Durham, North Carolina.

Company size
10,001+
Company stage
IPO
Headquarters
Durham, NC
Founded
1998

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