Senior Global Trial Manager at IQVIA

Durham, North Carolina, United States

IQVIA Logo
Not SpecifiedCompensation
Senior (5 to 8 years)Experience Level
Full TimeJob Type
UnknownVisa
Healthcare, Pharmaceuticals, Clinical ResearchIndustries

Requirements

  • Bachelor's Degree in health care or other scientific discipline (or equivalent combination of education, training, and experience)
  • 7 years of clinical research/monitoring experience (or equivalent combination of education, training, and experience)
  • Consolidated knowledge of project management practices and terminology
  • Good knowledge of applicable clinical research regulatory requirements (GCP, ICH guidelines)
  • Strong written and verbal communication skills, including good command of the English language
  • Problem-solving skills and the ability to handle conflicting priorities
  • Attention to detail and accuracy in work, with a results-oriented approach
  • Good influencing, negotiation, judgment, and decision-making skills, with effective mentoring and training abilities
  • Willingness to travel up to 25%

Responsibilities

  • Ensuring clinical delivery of assigned projects in compliance with regulatory requirements, customer contracts, and internal SOPs
  • Meeting project recruitment targets and developing appropriate recruitment strategies
  • Contributing to project risk mitigation plans and managing clinical risks throughout the project lifecycle
  • Ensuring clinical quality delivery by identifying quality standards, planning compliance measures, and managing clinical quality issues
  • Managing clinical aspects of project finances, including Estimate at Completion (EAC), and identifying additional service opportunities
  • Leading clinical teams to deliver large, global trials and managing internal and external stakeholders
  • Supporting milestone achievements and reporting to stakeholders as per project scope requirements
  • Managing the clinical team at the project level, including resourcing, talent planning, and providing project-related training

Skills

Clinical Trial Management
Project Management
GCP
ICH Guidelines
Regulatory Compliance
Risk Mitigation
Recruitment Strategies
Stakeholder Management
Team Leadership
Clinical Monitoring

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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