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Edc Specialist Jobs (NOW HIRING)

Clinical Informatics Specialist Salary Range: $24.00/hr. - $30.00/hr. Location: Baltimore, MD (On ... Reviews EDC case report forms, when available, for each study against the IRB approved protocol and ...

Clinical Informatics Specialist Salary Range: $24.00/hr. - $30.00/hr. Location: Baltimore, MD (On ... Reviews EDC case report forms, when available, for each study against the IRB approved protocol and ...

Clinical Informatics Specialist Salary Range: $24.00/hr. - $30.00/hr.Location: Baltimore, MD (On ... Reviews EDC case report forms, when available, for each study against the IRB approved protocol and ...

As a Regulatory Specialist, you'll work closely with internal teams, sponsors, CROs, and ethics ... Have experience with CTMS, EDC, or other document management systems. Why Centricity Research? Our ...

As a Research Nurse Specialist, you will collaborate with physicians, principal investigators ... Experience with electronic data capture (EDC) systems and electronic medical records (EMR)

Clinical Research Specialist Location: Manhattan, NYC Duration: 6 months (could go beyond) Job ... EDC systems. High organizational ability with strong attention to detail Flexibility with a team ...

Showing results 41-60

Edc Specialist information

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$9

$24

$48

How much do edc specialist jobs pay per hour?

As of Sep 10, 2026, the average hourly pay for edc specialist in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $28.85 per hour, depending on experience, location, and employer.

What are popular job titles related to Edc Specialist jobs?

For Edc Specialist jobs, the most frequently searched job titles are:

Specialist Clinical Development

South San Francisco, CA • On-site

Other

Re-posted 8 days ago


Job description

South San Francisco, CA
Contract Duration: 12-36 months
Rate: Negotiable
Salary: NA, $1.00
Responsibilities:

  • Excellent employment opportunity for a Specialist Clinical Development in the South San Francisco, CA area.
  • Participates in the development, review and implementation of departmental SOPs, templates and processes
  • Support budget and resource planning across assigned projects
  • Contribute to technical infrastructure of data management
  • Participate in CRO/vendor selection process for outsourced activities
  • Represents data management in study team meetings
  • Manages data management timelines to coordinate and synchronize deliverables with the overall study timelines
  • Generates and/or reviews/approves study documents (e.g. Data Management Plans, Case Report Forms, data transfer specifications, SAE and/or external data reconciliation plans, coding conventions, study protocols)
  • Executes and/or distributes data management metrics, listings, and reports, as required
  • Oversight of data management CRO/service providers on assigned studies
  • Monitors the progress of all data management activities on assigned studies to ensure project timelines are met
  • Provides training on the CRF completion guidelines and EDC system at Investigator meetings and to internal or external team members, as needed
  • Proactively identifies potential study issues/risks and recommends/implements solutions
  • Responsible for the accuracy and completeness of the clinical data collected during a clinical trial, able to work independently towards the assigned goal
  • Provide DM support to Statisticians and Statistical Programmers in production of clinical trial reports and other deliverables
Experience:
  • Bachelor degree in Life Sciences, Computer Sciences, Mathematics, or health-related field
  • Minimum of 5 years of SENIOR-LEVEL DM (i.e., Sr. CDA) experience in the pharmaceutical or biotechnology industry or equivalent; depth and exposure to DM related tasks considered in lieu of minimum requirement
  • CRO management experience desired
  • Competence in SAS programming a plus
  • Prior oncology/hematology experience highly desirable
  • Requires solid knowledge of clinical data management principles, clinical trials process and regulatory requirements
  • Excellent verbal/written and interpersonal skills required
  • Able to communicate and collaborate effectively with cross-functional teams in face-to-face conversation, by telephone, and by email