Associate Medical Director, Nephrology

IQVIA; Warszawa; On-site; PLN 242,000 - 514,000; Full time

Job summary

IQVIA is seeking an Associate Medical Director in Warsaw to provide medical, clinical and scientific advisory expertise across divisions. You will participate in Medical Science activities on trials and serve as a medical expert during project delivery, providing therapeutic insight to business development.

The role requires a medical degree with license, at least 5 years in clinical medicine, and fluent English.

Qualifications

• Medical Degree from an accredited medical school with a medical license
• Minimum of 5 years' experience in clinical medicine in addition to clinical trials experience
• Board certification and current knowledge of regulatory landscape are required
• Fluent English and extensive communication skills are essential

Responsibilities

• Serves as Global Medical Advisor on assigned projects and provides medical guidance to project leaders
• Reviews protocols, IDBs/CRFs and CSR during the trial lifecycle
• Provides medical support for sites and project staff on safety and eligibility issues
• Attends investigator meetings and participates in scientific advisory discussions
• May travel 15–20% and respond to urgent protocol questions 24/7 as needed

Skills

Fluent English

Strong communication

Clinical trials experience

Phase I experience

Business acumen

Education

Medical Degree

Medical License

Board Certified

Job description

Job Overview

The Associate 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.

Job Overview

The Associate 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 24/7 to respond urgent protocol-related questions from investigative sites, in accordance with local labor laws.
• May require regular travel (15%-20%)

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, in addition to 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.
• Business Acumen.
• Board Certified.
• Experience or knowledge in Phase I studies or early clinical development.
• Fluent English.
• Extensive communication skills.

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

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.

The potential base pay range for this role, when annualized, is 241.800,00 zł - 513.900,00 zł. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.