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IQVIA

Runs drug trials and sells health data to pharma

Medical Director - Rheumatologist

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeDurham, NC, USA

About the Job

Requirements

  • A medical degree from an accredited and internationally recognized medical school.
  • Board certification or eligibility in Rheumatology.
  • Typically, 3 to 5 years of prior relevant experience in the requested medical specialty area.
  • Previous clinical research experience as an investigator or in the pharmaceutical, contract research organization, or biotechnology industry.
  • Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
  • Strong communication, presentation, and interpersonal skills, including a good command of written and spoken English.
  • Robust and current knowledge of the scientific, clinical, regulatory, commercial, and competitive landscape in Rheumatology.
  • Proven skills in providing consultation and advice on multiple assignments.
  • Availability for intermittent domestic and foreign travel to support business assignments.

Responsibilities

  • Serve primarily as Medical Monitor at the global or regional level on assigned clinical trials.
  • Serve as Scientific Advisor to Project Leaders, providing medical advice and input on the medical and scientific aspects of assigned projects.
  • Provide medical support to investigative sites and project staff on protocol-related issues, including patient eligibility, adverse-event management, and patient disposition.
  • Provide therapeutic-area and indication training for the project clinical team.
  • Attend and present at Investigator Meetings.
  • Review and clarify trial-related adverse events.
  • Attend kick-off meetings, weekly team meetings, and client meetings as needed or requested.
  • Respond to urgent protocol-related issues at investigative sites.
  • Contribute to the development of medically related aspects of client proposals, including budgets related to medical monitoring.
  • Provide medical and scientific advice and guidance to internal stakeholders developing proposals, including reviewing protocols for scientific and regulatory soundness and feasibility, and identifying target-site and principal-investigator profiles.
  • Attend and present at bid defense meetings as required.
  • Travel periodically for regional and international assignments.

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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