Source Job

$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.

Data Management EDC Systems Clinical Research SAS

8 jobs similar to Clinical Data Manager

Jobs ranked by similarity.

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.

$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.

Perceptive helps the global biopharmaceutical industry bring new medical treatments to market faster. With a global team, they emphasize collaboration, growth, and winning together.

LATAM Mexico Brazil Argentina Chile Colombia Peru

  • Lead the development and optimization of clinical data systems, driving data standardization and building scalable validation frameworks.
  • Architect high-performance databases and ETL pipelines, integrating data from diverse clinical systems across global trials.
  • Serve as a strategic liaison between Biostatistics, Clinical Operations, and Regulatory Affairs to translate clinical requirements into technical solutions.

Precision Medicine Group is a specialized life sciences company that accelerates the development and delivery of precision medicine. It has a global workforce and fosters a collaborative, compliance-oriented culture focused on innovation and regulatory excellence.

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.

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.

US

  • Support implementation and sustainment activities for research-related Electronic Health Record (EHR) solutions across the VA research enterprise.
  • Administer surveys, gather requirements, maintain REDCap databases, and coordinate stakeholder communications to support study build activities.
  • Develop and maintain trackers, status reports, process documentation, and help ensure timely completion of assigned actions and milestones.

Aptive partners with federal agencies to achieve their missions through improved performance, streamlined operations and enhanced service delivery. Founded in 2012, the company has over 300 employees nationwide and supports agencies including Veterans Affairs, Transportation, Defense, Homeland Security and the National Science Foundation.

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.

US

  • Accountable for leading assigned clinical research activities and partnering with stakeholders on study design.
  • Conducts on-site and remote site visits, including qualification, initiation, monitoring, and close-out.
  • Tracks study progress, manages budgets, and mentors junior clinical study managers.

Intuitive is a pioneer and market leader in robotic-assisted surgery, dedicated to minimally invasive care. With over 25 years of experience, the company fosters an inclusive and diverse team culture where employees are empowered to do their best work.