Source Job

$52,520–$75,028/yr
US

  • Ensures clinical trial databases meet project requirements by attending sponsor meetings and managing data management deliverables.
  • Ensures proper execution of data management plans by collaborating with project team, defining edit checks, and maintaining documentation.
  • Ensures accuracy and consistency of clinical databases by reviewing data, resolving issues, and tracking outstanding items.

Clinical Data Management Database Management Problem Solving Collaboration

8 jobs similar to Clinical Data Manager

Jobs ranked by similarity.

$106,200–$179,700/yr
US

  • Manage design, development, implementation, validation, and support of clinical databases for pre-market or post-market clinical studies.
  • Collaborate with clinical operation teams to ensure high-quality research and database development adhering to departmental operating procedures.
  • Contribute to development of data management plans, EDC design, and data cleaning and review activities.

Intuitive is a global leader in robotic-assisted surgery and minimally invasive care, developing technologies like the da Vinci surgical system and Ion. The company is a large organization of engineers, clinicians, and innovators united to make surgery smarter, safer, and more human.

US Unlimited PTO

  • Lead sponsor-side clinical data management activities across CoMind's clinical development portfolio.
  • Design, build, and configure clinical study databases including eCRF design and database validation.
  • Serve as subject matter expert on regulatory expectations and manage vendor relationships.

CoMind develops non-invasive neuromonitoring technology for clinical brain monitoring. The company is an early-stage startup with an AI-driven culture.

Canada

  • Lead clinical data system implementation, configuration, and maintenance for complex research projects.
  • Serve as primary contact for internal teams, clients, and stakeholders on clinical system activities.
  • Support business development by providing technical expertise in client presentations and proposal discussions.

Our partner is a company focused on clinical research technology solutions. They operate globally with a collaborative and fast-paced culture.

Global

  • Provides study-level oversight and leadership for global clinical trials from inception through closure, managing vendors, recruitment, and cross-functional teams.
  • Develops and manages study materials including protocols, regulatory submissions, and budgets while ensuring compliance with quality standards and inspection readiness.
  • Contributes to system management like EDC, IRT, and eTMF, and supports process improvement initiatives or serves as a mentor.

AbbVie discovers and delivers innovative medicines and solutions to address serious health issues in immunology, oncology, neuroscience, and aesthetics. As a global biopharmaceutical company with a robust pipeline, they emphasize integrity and innovation, serving patients worldwide with a dedicated team.

$138,600–$173,300/yr
US

  • Manage all aspects of clinical trials from start-up through close-out, ensuring timelines, costs, and quality metrics are met.
  • Oversee vendor/CRO selection and management, study contracting, budgeting, and forecasting.
  • Lead study-related activities including protocol preparation, investigator selection, and training, and collaborate with cross-functional teams.

Natera is a global leader in cell-free DNA testing, dedicated to oncology, women’s health, and organ health. The team consists of highly dedicated professionals from world-class institutions who care deeply for their work and each other.

Europe

  • Ensure accuracy, consistency, and integrity of critical clinical trial data supporting life sciences and patient care.
  • Design, validate, and maintain project-specific clinical databases and data transfer processes.
  • Collaborate with clinical project teams and external partners to manage the full lifecycle of clinical data systems.

The company connects candidates with job opportunities using AI-powered matching. They process applications and share shortlisted candidates with hiring companies.

Europe

  • Manage and oversee all clinical aspects of trials across multiple countries, ensuring timeline adherence, quality, and scope.
  • Lead CRAs and collaborate with cross-functional teams to achieve high client satisfaction and smooth trial operations.
  • Identify risks, develop creative action plans, and maintain focus on study priorities through effective communication.

Precision for Medicine is a precision medicine CRO that combines novel trial designs, advanced biomarker analytics, and deep oncology expertise to accelerate drug development. The company fosters a dynamic, high-energy culture and values dedicated professionals who thrive in challenging environments.

  • Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.
  • Ensuring protocol compliance, data integrity, and patient safety throughout the trial process.
  • Collaborating with investigators and site staff to facilitate smooth study conduct.

ICON is a global healthcare intelligence and clinical research organization dedicated to accelerating the development of new medicines and treatments. As a values-driven company, ICON fosters a culture of integrity, collaboration, agility, and inclusion, employing a diverse workforce.