d) at IQVIA

Frankfurt, Hessen, Germany

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Not SpecifiedCompensation

Senior (5 to 8 years), Expert & Leadership (9+ years)Experience Level

Full TimeJob Type

UnknownVisa

Pharmaceuticals, Clinical ResearchIndustries

Requirements

Medical Degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education
Medical license, or equivalent, from the country or region in which he/she resides and works
Minimum of 5 years' experience in clinical medicine
Minimum of 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
Business Acumen
Board-certification for the required therapeutic
Knowledge of cardiology, metabolic diseases and nephrology
Experience or knowledge in Phase I studies or early clinical development
Fluent English
Extensive communication skills
May require regular travel (15%)

Responsibilities

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
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

Skills

Medical Degree

Medical Monitoring

Pharmacovigilance

Protocol Review

Adverse Event Review

SAE Review

Clinical Study Report

Investigator Meetings

Cardiology

Metabolic Diseases

Nephrology

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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