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Edc Project Manager information

See Novato, CA salary details

$45.2K

$120.6K

$190.2K

How much do edc project manager jobs pay per year?

As of Jun 15, 2026, the average yearly pay for edc project manager in Novato, CA is $120,555.00, according to ZipRecruiter salary data. Most workers in this role earn between $92,200.00 and $144,400.00 per year, depending on experience, location, and employer.

What are some common challenges faced by EDC Project Managers when implementing new electronic data capture systems?

EDC Project Managers often encounter challenges such as ensuring seamless integration of the new system with existing clinical trial workflows, managing diverse stakeholder expectations, and maintaining data quality throughout the study. They must also handle tight timelines and adapt quickly to regulatory changes or sponsor requirements. Effective communication with both technical teams and clinical staff is crucial to overcoming these obstacles and ensuring successful project delivery.

What are the key skills and qualifications needed to thrive as an EDC Project Manager, and why are they important?

To thrive as an EDC Project Manager, you need expertise in clinical data management, project coordination, and a solid understanding of Electronic Data Capture (EDC) systems, usually supported by a degree in life sciences or related fields. Familiarity with EDC platforms like Medidata Rave or Oracle InForm, along with certifications such as PMP or CDISC, is highly valuable. Strong organizational, problem-solving, and communication skills help you effectively lead cross-functional teams and manage client expectations. These competencies ensure successful EDC project delivery, regulatory compliance, and high-quality clinical trial data.

What are EDC Project Managers?

EDC Project Managers are professionals who oversee the planning, execution, and monitoring of projects related to Electronic Data Capture (EDC) systems, primarily within clinical research and pharmaceutical industries. They coordinate between cross-functional teams, manage timelines, ensure regulatory compliance, and address any issues that arise during the data collection process. Their goal is to ensure that EDC systems are implemented efficiently and effectively, supporting the overall success of clinical trials. EDC Project Managers also act as the main point of contact for sponsors and stakeholders, ensuring that project objectives and quality standards are met.

What is the difference between Edc Project Manager vs Electrical Project Manager?

AspectEdc Project ManagerElectrical Project Manager
CertificationsPMP, OSHA, EDC-specific trainingPMP, OSHA, Electrical licenses
Work EnvironmentEnergy, utility, and infrastructure projectsConstruction, industrial, and commercial electrical projects
Industry UsageCommon in energy distribution and utility sectorsCommon in construction and industrial sectors
Job FocusDistribution systems, substations, and energy deliveryBuilding wiring, electrical systems, and installations

The Edc Project Manager primarily oversees energy distribution and utility infrastructure projects, focusing on energy delivery systems. In contrast, the Electrical Project Manager handles a broader range of electrical construction projects, including commercial and industrial wiring. Both roles require similar certifications but differ in industry focus and project types.

What job categories do people searching Edc Project Manager jobs in Novato, CA look for? The top searched job categories for Edc Project Manager jobs in Novato, CA are:
What cities near Novato, CA are hiring for Edc Project Manager jobs? Cities near Novato, CA with the most Edc Project Manager job openings:
Edc Project Manager jobs near you

Senior Manager, Clinical Data Management

Latigo Biotherapeutics

San Francisco, CA • On-site

Full-time

Posted 12 days ago

Job description

POSITION DESCRIPTION

Latigo is seeking a Senior Manager of Clinical Data Management to lead and oversee data management activities for assigned clinical studies, which includes, but is not limited to: CRF design and development, CRF standardization, ongoing data review and cleaning, rolling/interim/final database locks, and clinical data archival. They will work collaboratively with other internal and external clinical study team members across Clinical Operations, Biostatistics, Clinical Development and Translational Science. They shall be adept at utilizing and managing EDC systems, managing clinical data workflows and processes, and ensuring clinical trial data integrity and quality in their assigned studies to ensure high quality data in support of analysis for regulatory submissions, safety reporting and publications.

Essential duties and responsibilities:

  • Manage and oversee CROs/vendors in clinical data management on clinical trials within assigned program.
  • Oversee the data management activities and deliverables from EDC build to final database lock and their timelines for assigned studies to ensure quality, efficiency and consistency.
  • Perform detailed reviews of data management specific plans and database specifications to ensure a built-in quality approach.
  • Perform User Acceptance Testing (UAT) on EDC, IRT and eCOA systems.
  • Develop study metrics reports and other reports as needed.
  • Work with vendors to set up and review data transfer specifications.
  • Oversee vendor data reconciliation (i.e. central laboratory data, SAE) to include quality control and timely review of queries.
  • Lead the creation of data review plans for internal cross-functional clinical data review activities.
  • Oversee EDC user administration and access for assigned studies.
  • Collaborate and communicate regularly with internal and external team members across other clinical trials and programs for consistency and standardization across programs to promote increasing efficiency.
  • Proactively identify potential issues affecting timeline, milestones, or deliverables, and propose strategies to mitigate or resolve.
  • Direct the development of CRFs and database design with cross-functional input and adherence to CDASH/CDISC standards and standards developed internally at Latigo Bio.
  • Participate in the creation of SOPs that are necessary for internal Clinical Data Management activities.
  • QC filing of data management documentation in the electronic Trial Master File (eTMF).
  • Maintain internal data management study level documentation in audit ready status, as applicable.
  • Perform other duties as requested.

Preferred Education & Experience:

  • Bachelor's degree required, at a minimum.
  • 7+ years of relevant industry experience in clinical data management.
  • Self-motivated and highly flexible individual with a proven track record of successfully managing multiple tasks and priorities within a fast-paced environment with minimal oversight.
  • Excellent project management skills.
  • Great attention to detail with excellent interpersonal, organizational, written and verbal communication skills.
  • Proficiency in EDC systems (i.e. Medidata Rave) and other integrated clinical systems (e.g., IxRS/IRT).
  • Working knowledge of ICH GCP and other regulatory guidance documents.
  • Working knowledge of CDISC/CDASH, GCDMP and other clinical data standards.

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