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Worldwide Clinical Trials

As a leading full-service global CRO, we work to create solutions that advance new treatments from discovery to reality.

Vice President, Data Management

Vice PresidentVice PresidentFull TimeRemoteLeadTeam 1,001-5,000H1B SponsorCompany SiteLinkedIn

Location

North Carolina

Posted

66 days ago

Salary

0

Seniority

Lead

Bachelor Degree15 yrs expExperience acceptedEnglishGoogle Cloud Platform

Job Description

Vice President, Data Management

Worldwide Clinical Trials

• Provide strategic leadership and executive oversight for the company’s global Data Management function. • Set the vision, operational framework, and standards that enable efficient, compliant, and high-quality data delivery across the organization. • Oversee department strategy, execution, and continuous improvement, ensuring real-time, efficient data flow that results in clean, analyzable databases. • Lead and develop high-performing teams, establishes and maintains robust processes and SOPs, and ensure readiness for client and regulatory audits. • Partner closely with cross-functional and executive stakeholders, evaluates key performance indicators, supports business development efforts, and maintains financial oversight of the department. • Hold full accountability for the recruitment, retention, and development of Data Management talent. • Act as the executive escalation point for project and client issues, fostering strong partnerships and positive client relationships. • Provide strategic input into business development, including RFP responses, bid defenses, and client presentations. • Represent the Data Management function internally and externally, including cross-functional forums, client meetings, and industry events.

Job Requirements

  • A minimum of 15+ years of relevant work experience.
  • A minimum of 5 years of relevant leadership experience in a Clinical Research Organization.
  • Strong working knowledge of the drug development process, ICH GCP guidelines, and FDA and/or international regulations and their application to clinical trials.
  • Deep knowledge of the drug development process, ICH GCP, and FDA and/or international clinical trial regulations.
  • Strong data management expertise with broad industry awareness.
  • Proven financial acumen, including budgeting, forecasting, and resource management.
  • Advanced proficiency with Microsoft Office and enterprise computer applications.
  • Excellent written, verbal, and presentation communication skills.
  • Strong organizational, analytical, and problem-solving abilities with sound judgment and decision-making skills.
  • Ability to manage multiple priorities, meet deadlines, and adapt effectively in a fast-changing environment.
  • Strong interpersonal skills with the ability to collaborate across all organizational levels and diverse teams.
  • Independent, results-driven leader and collaborative team player with a commitment to excellence, innovation, and high standards.
  • Degree in statistics preferred; however, a degree in science, mathematics, or a related field coupled with relevant work experience may be an acceptable substitute.

Benefits

  • Equal employment opportunities
  • Diverse talent priority
  • Inclusive environment
  • Cultivating collaboration and creativity

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