Clinical Research Physician at IQVIA

Shanghai, Shanghai, China

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, PharmaceuticalsIndustries

Requirements

Medical degree from an accredited and internationally recognized medical school with a curriculum relevant to general medical education
Specialty Board certification in relevant specialty area preferred
Typically 3-5 years of prior relevant experience in general clinical medicine including experience in the requested applicable medical specialty area or equivalent combination of education, training, and experience
Current knowledge of medical, scientific and clinical landscape in applicable therapeutic area
Good communication, presentation and interpersonal skills, including good command of English language (both written and spoken)
Ability to establish and maintain effective working relationships with coworkers, managers and clients
Attention to details, flexibility and ability to provide advice on multiple assignments
Current or prior license to practice medicine
Clinical experience in the requested medical specialty (board-certification for the required therapeutic area preferred)

Responsibilities

Primarily acts as back-up Medical Advisor but may serve as Regional Medical Advisor on 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
May contribute to the medical review of the protocol, Investigative Drug Brochure (IDB) and/or Case Report Forms (CRFs)
May provide therapeutic area/indication training for the project clinical team
Attends and may present 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

Skills

Key technologies and capabilities for this role

Medical DegreeBoard CertificationClinical MedicineAdverse Events ReviewProtocol ReviewPharmacovigilanceClinical Study ReportTherapeutic Area TrainingPatient SafetyInvestigator Meetings

Questions & Answers

Common questions about this position

What qualifications are required for the Clinical Research Physician role?

Candidates need a medical degree from an accredited school, specialty board certification preferred, 3-5 years of relevant clinical experience in the applicable specialty, current license to practice medicine, and clinical experience in the requested medical specialty.

What skills are essential for this position?

Key skills include good communication, presentation and interpersonal skills with command of English, ability to establish effective working relationships, attention to detail, flexibility, and current knowledge of the medical, scientific, and clinical landscape in the therapeutic area.

Is this a remote position or does it require office work?

This information is not specified in the job description.

What is the salary or compensation for this role?

This information is not specified in the job description.

What makes a strong candidate for this Clinical Research Physician position?

A strong candidate will have a medical degree, board certification in the relevant specialty, 3-5 years of clinical experience in the therapeutic area, current medical license, and strong communication skills with knowledge of the clinical landscape.

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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