Assoc. Medical Director, Rheumatologist

Job Overview

The Assoc. 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 rheumatologic 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: patients eligibility adverse events management patients disposition etc.

• 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.

• Attend and presents at bid defense meetings as required.

• Requires 5% periodic regional and international travel.

Qualifications:

• Medical degree from an accredited and internationally recognized medical school

• Board certified or eligible in Rheumatology

• 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 Rheumatology.

• 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.

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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements misrepresentations or material omissions during the recruitment process will result in immediate disqualification of your application or termination of employment if discovered later in accordance with applicable law. We appreciate your honesty and professionalism.

Required Experience:

Director

Employment Type : Full-Time
Experience: years
Vacancy: 1