Clinical Operations Program Manager - Sponsor-dedicated at IQVIA

Reading, England, United Kingdom

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Not SpecifiedCompensation

Senior (5 to 8 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, PharmaceuticalsIndustries

Requirements

Bachelor's degree preferred
Fluent in English, both written and verbal
At least 4-5 years of experience in the end-to-end global feasibility process in clinical trials
Experience in creating feasibility dashboards for stakeholders/clients
Excellent communication skills
Strong project planning and organizational capabilities
Proven ability to work independently or in a team setting to meet goals within budget, timeline, and compliance expectations
Knowledge of Good Clinical Practice and understanding of the overall drug development process
Strong skills in MS Office Suite, including MS Teams, Excel, Word, and expert-level PowerPoint slide creation and formatting

Responsibilities

Conduct early viability and feasibility assessments
Validate and refine allocation strategies, including scenario planning and risk management
Perform re-feasibility assessments as needed
Analyze external and internal data to validate and refine strategic allocation of assigned trials, ensuring alignment with program allocation strategy
Develop evidence-based scenario planning to drive realistic project timelines
Support the end-to-end feasibility process starting from early viability assessments, pre-IMB and trial feasibilities, and develop strategic allocation, site selection, and recruitment plans scenarios for assigned programs and trials
Prepare and coordinate briefing information, training resources, and other materials
Provide project planning support and manage key deliverables
Assemble actions, output summaries, and minutes for follow-up tracking
Lead feasibility activities, such as feasibility survey consolidation and analysis, and review data insights with feasibility teams
Coordinate and manage the editing, technical support resolution, and distribution of feasibility questionnaires at the trial level between sites, countries, and globally; ensure feedback from feasibility assessments is addressed
Conduct scenario planning and provide outputs from Footprint Optimizer (FPO) to assist with timeline review, validation of key data, and support for Final Allocation Curve as part of handover
Assist in portfolio management activities, including tracking tollgates and preparing for risk review sessions; draft risk slides and SPF overviews of current feasibility work for senior management
Ensure required end-of-feasibility information entry and compliance records into internal systems (e.g., IMPACT planning; archiving for Trial Master File and regulatory documents in CREDI/Subway)
Manage early timeline and pricing assessments, liaising with Health Insights and/or performing competitive intelligence searches to build assumptions (includes archiving outputs in team repositories)
Manage logistics for team meetings, including agenda preparation, minutes, and follow-up on action items

Skills

Feasibility Assessments

Scenario Planning

Risk Management

Data Analysis

Project Planning

Site Selection

Portfolio Management

Footprint Optimizer

Questionnaire 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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