Associate Medical Director- Endocrinologist, Home-Based

IQVIA; Roma; In loco; EUR 80.000 - 120.000; Tempo pieno

Descrizione del lavoro

An established industry player is seeking an Associate Medical Director to provide vital medical and scientific advisory expertise across various divisions. In this pivotal role, you will engage in all aspects of medical science throughout project lifecycles, ensuring patient safety and protocol integrity. This position requires a strong medical background, including a medical degree and board certification in Endocrinology, along with experience in clinical trials and therapeutic areas such as cardiology and obesity. Join a leading global provider dedicated to improving patient outcomes and advancing healthcare solutions.

Competenze

• Medical degree and license required, with 5+ years in clinical medicine.
• Specialty Board Certification in Endocrinology and experience in cardiology.

Mansioni

• Serve as Global Medical Advisor on assigned projects.
• Provide medical support for protocol-related issues and adverse events.
• Attend and present at Investigator Meetings.

Conoscenze

Medical Advisory

Clinical Medicine

Therapeutic Expertise

Regulatory Knowledge

Communication Skills

Formazione

Medical Degree

Specialty Board Certification in Endocrinology

Descrizione del lavoro

Job Overview

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

Essential Functions

Medical Monitoring:

• Primarily serves as 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.
• May require periodic travel.
• Extensive use of telephone and face-to-face communication requiring accurate perception of speech.

Qualifications & 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 is required, plus a minimum of 5 years' experience in clinical medicine.
• Specialty Board Certification in Endocrinology required.
• Experience in cardiology and obesity.
• Nice to have ; 4 years' clinical trials experience as an investigator or in the Pharma, CRO, or Biotech industry.
• Robust and current knowledge of scientific, clinical, regulatory, commercial, and competitive landscape in applicable therapeutic area.
• Knowledge of applicable federal and local regulations and guidelines pertaining to clinical research.

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