About the Company
IQVIA (NYSE: IQV) is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are committed to pushing the boundaries of human science and data science to make the greatest positive impact on human health. With operations in more than 100 countries and 88,000+ employees worldwide, IQVIA is a Fortune 500 company and a global leader in clinical research.
Job Description
We are seeking an experienced and dedicated Clinical Trial Manager to join our dynamic team in Washington D.C. In this pivotal role, you will be responsible for the overall operational management and successful execution of clinical trials, ensuring adherence to protocols, Good Clinical Practice (GCP), and all regulatory requirements. This position requires strong leadership, organizational skills, and a commitment to advancing medical research. A comprehensive relocation package is available for eligible candidates moving to the Washington D.C. area.
Key Responsibilities
- Manage and oversee the planning, execution, and close-out of assigned clinical trials.
- Develop, manage, and track trial budgets, timelines, and resources.
- Lead and motivate cross-functional project teams, including CRAs, data managers, and statisticians.
- Ensure trial activities comply with study protocols, GCP, SOPs, and regulatory guidelines.
- Select, manage, and oversee third-party vendors (e.g., CROs, central labs, IRBs).
- Monitor study progress, identify potential risks, and implement mitigation strategies.
- Prepare and review essential trial documents, including protocols, informed consent forms, and study manuals.
- Facilitate communication and collaboration between internal teams, investigators, and external partners.
- Participate in the selection, initiation, and close-out of clinical sites.
- Oversee data collection, data quality, and timely database lock activities.
- Ensure timely and accurate reporting of trial progress and safety information.
Required Skills
- Minimum of 4 years of experience in clinical trial management within a pharmaceutical company, CRO, or academic institution.
- Demonstrated knowledge of Good Clinical Practice (GCP) and relevant regulatory requirements (e.g., FDA, EMA).
- Proven ability to manage complex clinical trials from initiation to close-out.
- Strong project management and organizational skills.
- Excellent written and verbal communication abilities.
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Outlook) and clinical trial management systems.
- Ability to lead and motivate cross-functional teams.
- Problem-solving and decision-making capabilities.
Preferred Qualifications
- Bachelor's degree in a life science, health-related field, or equivalent experience.
- Advanced degree (Master's, Ph.D.) in a scientific or health-related discipline.
- Certification in Clinical Research (e.g., CCRP, PMP).
- Experience in specific therapeutic areas such as Oncology, Cardiology, or Neuroscience.
- Familiarity with electronic data capture (EDC) systems and eTMF platforms.
Perks & Benefits
- Competitive salary and performance-based bonuses.
- Comprehensive health, dental, and vision insurance plans.
- Generous paid time off and holidays.
- 401(k) retirement plan with company match.
- Life and disability insurance.
- Professional development and continuing education opportunities.
- Employee assistance program.
- A comprehensive relocation package to support your move to Washington D.C.
How to Apply
If you are interested in this position, please click the "Apply Now" button below. To ensure your application is properly considered, please prepare the following:
- An up-to-date Resume or CV
- A brief cover letter summarizing your experience and motivation
Applications are reviewed on a rolling basis. Only shortlisted candidates will be contacted for an interview.
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