(Associate) Medical Director at IQVIA

Beijing, Beijing, China

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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

Key technologies and capabilities for this role

Medical MonitoringProtocol ReviewAdverse Event ReviewSerious Adverse EventsClinical Study Report ReviewInvestigator MeetingsTherapeutic Area TrainingMedical StrategyPatient SafetyInclusion/Exclusion Criteria

Questions & Answers

Common questions about this position

What is the salary for the (Associate) Medical Director position?

This information is not specified in the job description.

Is this role remote, hybrid, or onsite?

The position is onsite or hybrid with travel required, including periodic international travel.

What are the key requirements for this role?

Candidates need a medical degree from an accredited medical school, a medical license from the country or region of residence and work, and at least 5 years of experience in clinical medicine.

What does the work environment involve for this position?

The role requires availability 24/7 for urgent protocol-related issues and periodic international travel.

What makes a strong candidate for the Medical Director role?

A strong candidate will have a medical degree, active licensure, and at least 5 years of clinical medicine experience to handle medical monitoring and strategy responsibilities effectively.

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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