Global Trial Manager (Program, Strategy and Planning) at IQVIA

Reading, England, United Kingdom

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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, Life Sciences, HealthcareIndustries

Requirements

Leadership skills in a matrix environment, with multidisciplinary and networking teams
Excellent negotiation and conflict resolution skills and enterprise mindset
Clinical Trial Team (CTT) experience
GCO sub team experience

Responsibilities

Executes and delivers the GCO supported clinical studies; guides planning and decision making at study level
Acts as the CTT product owner with clear and focused duties and responsibilities per the agile ways of working
Active member of a Clinical Operations community within PSP supporting the COPH and SL
Promotes operational excellence in the development of global clinical study protocol(s), clinical study report(s), and other study-related documents
Support study start up activities, as needed
Deliver patient recruitment, clinical data, study documentation and study reports
Proactive, iterative operational planning with effective contingencies and embedded risk management mindset in CTT

Skills

Key technologies and capabilities for this role

Clinical TrialsStudy Start UpPatient RecruitmentProtocol DevelopmentClinical Study ReportRisk ManagementLeadershipNegotiationConflict ResolutionMatrix ManagementAgileCTTGCO

Questions & Answers

Common questions about this position

What is the employment type for this role?

This is a full-time position.

Is this role remote or does it require office work?

This information is not specified in the job description.

What key skills are required for the Global Trial Manager role?

Key skills include leadership in a matrix environment with multidisciplinary teams, excellent negotiation and conflict resolution skills, and an enterprise mindset.

What is the company culture like at IQVIA?

IQVIA emphasizes operational excellence, agile ways of working, and creating intelligent connections to accelerate medical treatments and improve patient outcomes worldwide.

What makes a strong candidate for this position?

Strong candidates will have leadership skills in matrix environments, negotiation and conflict resolution expertise, and experience with Clinical Trial Teams (CTT) and GCO sub teams.

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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