ZipRecruiter

Log In

1

Clinical Data Management Rave Programmer Jobs (NOW HIRING)

next page

Showing results 1-20

All JobsTechnology JobsData JobsData Architect JobsClinical Data Management Rave Programmer Jobs

Clinical Data Management Rave Programmer information

See salary details

$24

$64

$102

How much do clinical data management rave programmer jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for clinical data management rave programmer in the United States is $64.77, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $73.32 per hour, depending on experience, location, and employer.

What are popular job titles related to Clinical Data Management Rave Programmer jobs?

For Clinical Data Management Rave Programmer jobs, the most frequently searched job titles are:

Infographic showing various Clinical Data Management Rave Programmer job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, and 3% Contract. Highlights an 88% Physical, 2% Hybrid, and 10% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.

Associate Director, Clinical Data Management

Redwood City, CA

Corcept Therapeutics
Biotechnology Research and Development • 51 - 200 employees
Learn more about Corcept Therapeuticsexternal

$229K - $269K/yr

Full-time

Re-posted 14 days ago

Job description

The Associate Director, Clinical Data Management ensures optimized data collection, flow and access across EDC and non-EDC data sources. Responsible for accuracy, completeness and CDISC compliance of Corcept clinical databases.

 Responsibilities:

  • Works in cooperation with Director of Clinical Data Management to select and maintain preferred vendor network for data management activities
  • Reviews, proposes and obtains bids for tools enabling real-time data visualization, interrogation, and reporting
  • Manages strategic input into the design of data flow across EDC and non-EDC data sources across vendor network
  • Manages data management service providers to ensure the quality of deliverables and that timelines are met
  • Develops and contributes to the design of processes enabling near-real-time data access for Corcept clinical trials
  • Ensure data quality of clinical database through implementation of CDISC compliance
  • Reviews and critically assesses data query resolution metrics and suggests process improvement
  • Reviews study protocols to ensure that data collection and CRF design meet study objectives
  • Manages and oversees SAE reconciliation between clinical and pharmacovigilance database
  • Review clinical data for completeness, accuracy, and consistency in accordance with the investigational plan
  • Provide subject matter expertise to project team members during all phases of project life cycle
  • Provides accurate and timely clinical data to internal and external customers upon request
  • Manage development, test, and maintain data management systems
  • Manage development and periodic review of Data Management specific SOPs, WIs and templates
  • Provide subject matter expertise prior, during, and post internal and external audits and inspections
  • Maintain compliance with company and study-specific learning requirements

Preferred Skills, Qualifications or Technical Proficiencies:

  • Master's Degree in health care or life sciences preferred
  • Relational database experience, SQL, SAS, and clinical data management systems
  • Knowledge and experience with MedDRA, WHODrug and other Thesaurus classification of controlled management systems
  • Knowledge of CDISC/SDTM. Hands-on experience preferred
  • Hands-on experience working with mainstream EDC systems (e.g. Rave, Medrio, Inform)
  • Familiarity with Data Visualization Tools for quick customized data access (e.g Spotfire, Tableau, RShiny)
  • In-depth understanding of Data Management regulatory guidelines: ICH, GCDMP, 21CFR Part 11
  • Demonstrated strong management abilities for project and staff management of Data Management Deliverables in clinical development

Preferred Education and Experience:

  • Bachelors or higher in science, math or computer science
  • 10+ year experience in clinical trial industry (med device, pharma or biotech)
  • 10+ year experience in data management in clinical trial industry (med device, pharma or biotech)
  • Minimum of 3 years experience in preparing, executing, and finalizing Medical Coding (MedDRA and WHODrug) within the Medidata Rave Coder system
  • Strong knowledge of the MedDRA and WHODrug dictionaries along with their uprevisions
  • Experience in IT-related field a plus
  • Experience with Endocrinology clinical trials and CDISC therapeutic area standards
  • Experience with management of data flow and curation of biomarker data a plus
  • Experience managing Data Management CROs
  • Direct report management and oversight

The pay range that the Company reasonably expects to pay for this headquarters-based position is $229,300 - $269,800; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.

Apply