Clinical Project, Feasibility Analytics Manager at IQVIA

Durham, North Carolina, United States

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Not SpecifiedCompensation

Mid-level (3 to 4 years), Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, PharmaceuticalsIndustries

Requirements

Bachelor’s degree required
Minimum 3+ years of pharmaceutical industry experience in roles such as data procurement, business development, data strategy, or similar
3+ years as part of a clinical trial feasibility team at a pharma or CRO
Direct feasibility experience preferred
Advanced PowerPoint skills and intermediate Excel proficiency
Strong organizational skills and ability to manage multiple projects
Understanding of assigned therapeutic area
Ability to analyze survey results and compile insights
Excellent written and verbal communication skills, including compelling slide design
Proven success working within a matrix organization to deliver high-quality outputs
Extensive experience in feasibility analytics interpretation

Responsibilities

Ensure all services adhere to policies, local regulatory requirements, and ICH-GCP guidelines
Collaborate with Global Program Leads (GPLs), Global Trial Leads (GTLs), and study teams to execute feasibility-related objectives
Perform feasibility activities including: program/protocol feasibility, country and site selection, data compilation and analytics development, creation of presentation-ready slides for study teams
Develop integrated feasibility plans aligned with study objectives and timelines
Partner with analytics teams, study team members, and country contacts to deliver feasibility outputs on time and with high quality
Support survey distribution, follow-up, and response analysis
Assist with site list development, management, and communication
Generate content for newsletters and other communications to ensure successful execution of feasibility processes
Act as a Global Feasibility Lead within a therapeutic area, managing a book of work autonomously
Lead end-to-end feasibility processes for assigned studies
Collaborate with cross-functional teams to identify risks and implement mitigation strategies
Monitor progress against feasibility timelines and proactively communicate updates to stakeholders
Contribute to lessons learned and best practices for continuous improvement
Support staff development and mentor less experienced team members on feasibility processes

Skills

ICH-GCP

feasibility analysis

clinical trial planning

protocol feasibility

country selection

site selection

data analytics

survey analysis

project management

risk mitigation

stakeholder communication

cross-functional collaboration

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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