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Worldwide Clinical Trials is a global contract research organization that supports pharmaceutical and biotechnology companies throughout the drug development lifecycle. With more than 30 years of experience, the company provides clinical monitoring, data management, patient recruitment, and regulatory consulting across therapeutic areas including oncology, cardiology, and rare diseases. Its approach combines broad clinical trial expertise with personalized support and tailored solutions for complex studies.
Clinical Data Management Manager – United States Remote
Lead clinical data management teams, study delivery, budgets, quality, and process improvement for Worldwide Clinical Trials. The role combines team leadership, sponsor engagement, and operational oversight within a global contract research organization.
United States
California
Connecticut$99,000 – $196,000 / year
RemoteFull-timeSeniorLeadEnglish RequiredClinical ResearchDescription
- Lead assigned clinical data management teams and projects, overseeing study execution and budgets
- Serve as the main contact for internal and external escalations related to assigned studies
- Represent Worldwide Clinical Trials in sponsor governance meetings
- Assign staff to projects based on their capabilities and competencies
- Provide team oversight, training, mentoring, and career development support
- Confirm appropriate project resourcing and address operational or budget risks
- Handle performance-related escalations involving team members
- Communicate upcoming staff availability to Data Management leadership to support utilization continuity
- Assist Business Development with proposals and sponsor presentation materials
- Participate in sponsor audits, regulatory inspections, and third-party meetings
- Act as a subject matter expert for assigned Data Management processes when needed
- Evaluate and improve process effectiveness and efficiency
- Deliver process training and serve as a central contact for related questions
- Lead quality issues, including root-cause analysis and CAPA activities when required
- Maintain and revise QMDs and other process guidance documents
- Coach and mentor members of the Data Management department
- Direct departmental process improvement and efficiency initiatives
- Complete additional duties as assigned
Requirements
- Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a related field, or equivalent relevant experience
- At least nine years of clinical data management or related experience in the pharmaceutical, biotechnology, or medical device industry
- Two to four years of line management experience
- Expertise in clinical-trial data management best practices and technologies
- Advanced knowledge of clinical trial operations and protocol documents, including protocols, statistical analysis plans, CRFs, and study reports
- Strong project management capabilities, including oversight of data management teams, operations, and budgets
- Experience with recruitment, career development, and performance reviews as a line manager
- Exceptional attention to detail
- Strong written and verbal communication abilities
- Effective interpersonal and communication skills for working with cross-functional internal and external teams
- Ability to analyze issues and solve problems independently
Benefits
- Benefits package varies by location
- Transparent compensation practices with a focus on pay equity
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