Skip to main content

Medical Advisor, Associate Medical Director, Immunology & Internal Medicine, Europe

Apply now
Primary Location: Sofia, Bulgaria Additonal Locations: Barcelona, Spain,ESP; Bratislava, Slovakia,SVK; Kaunas, Lithuania,LTU; Kiev, Ukraine,UKR; Milan, Italy,ITA; Oeiras, Portugal,PRT; Prague, Czech Republic,CZE; Riga, Latvia,LVA; Tallinn, Estonia,EST; Warsaw, Poland,POL; Zagreb, Croatia,HRV Full time R1178119

Job description

Medical and Scientific Services has an exciting opportunity within the Immunology & Internal Medicine area medical group.  Let your career soar with IQVIA!

The Medical Advisor / Associate Medical Director will provide medical and scientific advisory expertise to all IQVIA divisions as requested. Participate in all aspects of Medical Science involvement on assigned clinical trials in the preparation of and during project delivery lifecycle. Provide medical expertise to business development activities.

Responsibilities:

The role includes predominantly Medical Monitoring responsibilities with Medical Strategic inputs.

Medical Monitoring:

  • Primarily serves as regional and/or global Medical Advisor on assigned projects.
  • Serves as Scientific Advisor and provides guidance 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 protocol clarifications, inclusion/exclusion determinations, and issues of patient safety and/or eligibility.
  • Performs medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs).
  • 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).
  • May perform medical case review of Serious Adverse Events (SAEs), including review of case documentation and patient narrative, in collaboration with the Pharmacovigilance department.
  • May provide medical support for the Analysis of Similar Events (AOSE), in collaboration with or on behalf of Pharmacovigilance department.
  • May perform medical review of adverse event coding.
  • Performs review of the Clinical Study Report (CSR) and patient narratives.
  • Attends Kick-Off meetings, weekly team meetings, and client meetings, as needed or requested.
  • Available 24 hours per day, 7 days per week to respond to urgent protocol-related issues at the investigative sites.

Medical Strategy:

  • Provides expert advises to the development of medically sounded delivery strategies for small to large and/or complex multi-region studies in partnership with sales and other functions responsible for business development activities.
  • Responsible for the development of the medically related aspects of client proposals including the budget related to medical monitoring.
  • Provides medical and scientific advises to key internal stakeholders developing proposals: this may include, but is not limited to, 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 meeting, as required.
  • Participates in strategic business development activities including presentations to prospective clients.
  • Maintains awareness of industry development and may author related publications.

Requirements:

  • Medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education, along with a medical license, or equivalent, from the country or region in which he/she resides and works.

  • Specialty Board certification in dermatology, or gastroenterology or rheumatology or an internal medicine with minimum of 2 years practicing medical experience in this area is necessary. Ideally experience in clinical trials either as investigator, coinvestigator or from working either for pharma or CRO, ideally as a medical monitor.

  • Excellent command of written and spoken English especially in medical terminology

  • Strong communication, presentation and interpersonal skills
  • Ability to establish and maintain effective working relationships with co-workers, managers and clients in an international environment
  • Ability in providing consultation and advice on multiple assignments are required, as well as initiative and flexibility
  • Robust and current knowledge of medical, scientific and therapeutic competitive landscape in applicable therapeutic area
  • Medical monitoring experience would be an advantage
  • May require periodic international travel
  • Extensive use of telephone and face-to-face communication requiring accurate perception of speech.
  • Extensive use of keyboard requiring repetitive motion of fingers.

LI-MS8

At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at jobs.iqvia.com.

Apply now

Join IQVIA’s Talent Network

Let’s stay connected. Join our global Talent Network to receive alerts when new opportunities become available that match your career ambitions.

Join our network
Top of page