Analytical Monitor - Base Level at IQVIA

Reading, England, United Kingdom

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, PharmaceuticalsIndustries

Requirements

Bachelor's degree (e.g., BS, BA) or equivalent professional experience, preferably in Health Sciences or Data Sciences
Approximately 4+ years of experience in Pharmaceutical, CRO or Biotech industry or related field
Experience with data analysis
Knowledge of clinical drug development within the pharmaceutical industry or related industry
Working knowledge of regulatory guidelines (e.g., ICH-GCP)
Experience working with technology platforms and systems used for the collection, analysis and reporting of data
Ability to collaborate in an environment of cross-functional stakeholders, plan and coordinate tasks effectively
Ability to communicate effectively in English (written and verbal)
Preferred Experience
Familiarity with basic risk management, project management, and/or statistical concepts
Basic Knowledge of Central Monitoring and Risk-based Quality Management (RBQM)/Risk-based Monitoring (RBM)/Quality by Design (QbD) concepts

Responsibilities

Conducts activities in compliance with sponsor functional SOPs, processes and policies
Facilitates smooth and effective communication, managing multiple communication streams. Follows agreed escalation pathways where needed
May support innovation or process improvement projects which may include but are not limited to participation in requirements development, user acceptance testing and identification of improvements to existing and new analytical tools & processes
Performs analytical monitoring activities for clinical trials within assigned scope of responsibility in line with portfolio timelines and priorities, including support of execution and close-out as outlined in the end-to-end process
Conducts regular (fit for purpose) reviews at site and subject level that will help early detection of issues, and prevent recurrence
Collaborates closely with the Site Manager and Central Monitoring Manager to action trends and signals detected at the site and subject level
Accesses various systems, databases and reporting tools to identify potential risks related to the site and subject level data quality, study participant safety and compliance by identifying trends and early warning signals
Provides timely analytical data insights to support the Site Managers in making decisions on site prioritization and critical engagement

Skills

data analytics

risk identification

risk mitigation

clinical trials

analytical monitoring

site monitoring

subject level review

data quality

SOP compliance

communication

escalation pathways

process improvement

user acceptance testing

reporting tools

databases

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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