Centralized Monitor at IQVIA

Dalian, Liaoning, China

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Not SpecifiedCompensation

Mid-level (3 to 4 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, PharmaceuticalsIndustries

Requirements

Experience in clinical trial monitoring or data management is required
Ability to perform Subject Level Data Review independently and with dual responsibilities
Proficiency in remote monitoring techniques
Strong analytical skills for study-specific analytics and trend analysis
Understanding of clinical study protocols, SOPs, and regulations
Ability to identify and escalate clinical study alerts
Excellent communication and collaboration skills

Responsibilities

Manage assigned sites and perform Subject Level Data Review
Conduct remote monitoring visits for assigned sites
Perform thorough data reviews, including inclusion/exclusion criteria, IP/AE/Labs/EOT/EOS/Endpoints/SAEs
Perform study-specific analytics and contribute to developing new analytics proposals
Manage operational insights of assigned sites/studies and complete study/site metrics trending
Provide inputs to clinical study teams, key decision makers, and internal team members
Ensure complete and accurate documentation of site-specific tools and templates
Perform centralized monitoring activities and evaluate site quality
Ensure accurate completion and maintenance of internal systems and databases
Manage triggers and preparation of i-site packs
Provide backup support to relevant stakeholders
Conduct periodic review of site-level KRIs and historic site performance
Monitor site performance and recommend timely corrective actions
Work in accordance with Study Central Monitoring Plan and relevant regulations

Skills

Clinical Trial Monitoring

Data Management

Remote Monitoring

Subject Level Data Review

Study-Specific Analytics

Trend Analysis

Clinical Protocols

SOPs

Regulations

KRI Monitoring

Site Management

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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