Program Delivery Management - Sponsor Dedicated at IQVIA

Paris, Île-de-France, France

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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 in pharmacy/nursing, with an active license. Advanced degrees in a scientific discipline and/or master’s degree are preferred
Minimum of 5 years’ experience in compounding/nursing in clinical or hospital setting. Oncology experience required; Immunology experience preferred
Minimum of 5 years’ experience in clinical research acquired in pharmaceutical industry, CRO or investigational site
Early Development/First-in-human previous clinical trial experience is required
Strong knowledge of drug development, clinical research operations and regulatory requirements, including ICH-GCP, GMP and applicable regulations
Familiarity with global site practices is required
Required experience with training needs assessment, development, and facilitation of training programs with clear learning objectives
Experience in preparation of novel pharmaceutical therapies such as gene-therapy or radiopharmaceuticals
Experience in leadership role, demonstrating ability to develop and implement strategies, and to foster teams
Excellent organizational skills and the ability to collaborate and handle multiple priorities within a matrix environment

Responsibilities

Oversight of studies and focus on investigational product preparation/administration within assigned therapeutic area to ensure alignment/consistency across the portfolio
Support development of high-quality training solutions by leveraging a variety of techniques for transfer of IP preparation/administration knowledge, may include other study specific related topics
Provides consultation as Subject Matter Experts through the training strategy process to produce high-quality education materials
Facilitate assessment of training needs as applicable with various teams to define plans with clear learning objectives
Lead internal, sponsor staff training and provide intensive support depending on IP complexity. Act as the main point of contact for resolution of any questions associated with IP
Contribute to training or IP process initiatives that can support the business
Demonstrates strong presence and authority, leading discussions and ensuring training strategy meets all quality, regulatory, and operational expectations
Monitor key risk IP indicators, escalate, and mitigate as required
Persuasively communicates with relevant internal stakeholders. Confidently advocates for best practices, ensuring all stakeholders adhere to high-quality standards
Takes decisive action to resolve inconsistencies, challenge unclear guidance, and escalate concerns when necessary
Portfolio support may involve travel to support training initiatives
Study portfolio oversight of advanced and highly complex preparation and administration techniques
Intensively involved in training or IP process initiatives to support the business with minimal guidance from organization leaders

Skills

Key technologies and capabilities for this role

Program Delivery ManagementInvestigational Product OversightIP Training StrategyStakeholder EngagementProtocol TrainingStudy StartupTraining Materials DevelopmentSubject Matter ExpertiseTraining Needs AssessmentGCO Site Management

Questions & Answers

Common questions about this position

What qualifications are required for this role?

A Bachelor’s degree in pharmacy or nursing with an active license is required.

Is travel required in this position?

Yes, portfolio support may involve travel to support training initiatives.

What is the employment type for this job?

The position is full time.

What key skills are needed for success in this role?

Excellent organizational skills, the ability to collaborate and handle multiple priorities within a matrix environment, strong communication, and leadership presence are required.

What are the main responsibilities of this position?

Responsibilities include oversight of investigational product preparation/administration, developing training solutions, providing consultation as a subject matter expert, leading training sessions, acting as the main point of contact for IP questions, and monitoring key risk indicators.

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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