(Associate) Medical Director at IQVIA

Beijing, Beijing, China

IQVIA Logo
Not SpecifiedCompensation
Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Clinical Research, Pharmaceuticals, HealthcareIndustries

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 the individual resides and works
  • Minimum of 5 years of experience in clinical medicine

Responsibilities

  • Serves as Global and/or Regional Medical Advisor on assigned projects
  • Provides scientific advice and guidance to Project Leaders on medical and scientific aspects of projects
  • Provides medical support to investigative sites and project staff, including protocol clarifications, inclusion/exclusion determinations, and patient safety and eligibility issues
  • Reviews protocols, Investigative Drug Brochures (IDB), and Case Report Forms (CRFs)
  • Provides therapeutic area/indication training for the project clinical team
  • Attends and presents at Investigator Meetings
  • Reviews and clarifies trial-related Adverse Events (AEs)
  • May perform medical case review of Serious Adverse Events (SAEs)
  • May provide medical support for the Analysis of Similar Events (AOSE)
  • Reviews adverse event coding
  • Reviews the Clinical Study Report (CSR) and patient narratives
  • Available 24/7 to respond to urgent protocol-related issues
  • Provides expert advice on the development of medically sound delivery strategies for clinical studies
  • Responsible for the medical and scientific aspects of client proposals, including budget allocation
  • Provides medical and scientific advice to internal stakeholders developing proposals (e.g., reviewing protocol scientific/regulatory soundness)
  • Participates in strategic business development activities, including presentations to prospective clients
  • Maintains awareness of industry developments and may author related publications
  • Attends bid defense meetings as required

Skills

Medical Monitoring
Protocol Review
Adverse Event Review
Serious Adverse Events
Clinical Study Report Review
Investigator Meetings
Therapeutic Area Training
Medical Strategy
Patient Safety
Inclusion/Exclusion Criteria

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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