Key Facts

Remote From:

Greece , Estonia , Ukraine , Hungary , Bulgaria , Romania , Portugal , Spain , United Kingdom , Slovakia , Czechia , Slovenia , Serbia

Full time

Expert & Leadership (>10 years)

English

Hard Skills

Clinical Monitoring Medical Oncology Clinical Documentation Patient Safety Clinical Medicine Adverse Event Monitoring Pharmacovigilance Online Communication Consensus Decision Making Presentation Training

Other Skills

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Non-Verbal Communication
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Multitasking
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Social Skills
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Self-Motivation

Roles & Responsibilities

Medical degree from an accredited medical school with curriculum relevant to general medical education.
5-7 years of experience in clinical medicine.
Board certification or qualifications in medical oncology, radiation oncology, hematology, or internal medicine with hematology/oncology experience.
Ability to work independently in a multidisciplinary matrix environment with excellent oral and written communication skills.

Requirements:

Serve as Global Medical Advisor and Scientific Advisor on assigned oncology projects, providing medical and scientific guidance to project leaders and cross-functional teams.
Conduct medical monitoring and review of protocols, IDBs, and CRFs; handle protocol clarifications, eligibility determinations, patient safety, and AE/SAE management in collaboration with Pharmacovigilance.
Provide therapeutic area training for the project clinical team; attend Investigator Meetings; review CSR and patient narratives.
Provide medical support for business development activities and client meetings; be available 24/7 for urgent protocol-related questions; travel as required.

IQVIA

Health Care

About IQVIA

IQVIA (NYSE:IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. IQVIA Connected Intelligence™ delivers powerful insights with speed and agility — enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients. With approximately 86,000 employees, IQVIA conducts operations in more than 100 countries. IQVIA is a global leader in protecting individual patient privacy. The company uses a wide variety of privacy-enhancing technologies and safeguards to protect individual privacy while generating and analyzing information on a scale that helps healthcare stakeholders identify disease patterns and correlate with the precise treatment path and therapy needed for better outcomes. IQVIA’s insights and execution capabilities help biotech, medical device and pharmaceutical companies, medical researchers, government agencies, payers and other healthcare stakeholders tap into a deeper understanding of diseases, human behaviors and scientific advances, in an effort to advance their path toward cures. To learn more, visit www.iqvia.com.

Company type: Large

Industry: Health Care

Founded: 2018

Company size: 10001

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Job description

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 24/7 to respond urgent protocol -related questions from investigative sites, in accordance with local labor laws.
May require regular travel.
Extensive use of keyboard requiring repetitive motion of fingers.
Extensive use of telephone and face-to-face communication requiring accurate perception of speech.

Qualifications

Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education.
5-7 years of experience in clinical medicine
Ability to work in partnership with a multidisciplinary group of colleagues, including translating concepts into practical approaches and promoting consensus.
Outstanding ability to work independently with minimal supervision, ability to work effectively within a team, and matrix environment.
Ability to organize and work efficiently on several projects, each with specific requirements and/or shifting priorities.
Excellent oral and written communications skills as well as interpersonal skills are essential.
Board certification or board qualifications in medical oncology, radiation oncology, hematology or internal medicine (with hematology or oncology experience)

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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.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.