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Medidata Rave Developer Jobs (NOW HIRING)

Clinical Data Analyst, Spotfire

Redmond, WA ยท On-site

$90K - $130K/yr

Experience with SAS/R, SQL programming, and data manipulation. * Familiarity with clinical trial ... Experience integrating Spotfire with clinical databases and EDC systems (e.g., Medidata RAVE ...

Clinical Data Associate

Redmond, WA ยท On-site

$75K - $95K/yr

Exposure to a Clinical EDC system (e.g., Medidata Rave, Veeva EDC) preferred. * SAS, Python, and R programming knowledge is a plus. * Familiarity with CDISC standards (CDASH, SDTM) and GCP guidelines ...

Clinical Data Associate

Redmond, WA ยท On-site

$75K - $95K/yr

Exposure to a Clinical EDC system (e.g., Medidata Rave, Veeva EDC) preferred. * SAS, Python, and R programming knowledge is a plus. * Familiarity with CDISC standards (CDASH, SDTM) and GCP guidelines ...

Clinical Data Manager

Redmond, WA ยท On-site

$100K - $170K/yr

Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * SAS programming experience. * Experience with managing Lab Data, such as PK, PD, and Biomarkers. * Detail-oriented ...

Sr. Director, Clinical Science (Oncology)

San Diego, CA ยท On-site

$84K - $115K/yr

More than 20 XmAb drug candidates engineered with our technology are in clinical development, and ... MS Office Suite, Visio, GraphPad Prism, Spotfire, Medidata RAVE, Inform etc. * Ability to work ...

Clinical Data Manager

Redmond, WA ยท On-site

$100K - $170K/yr

Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC). * SAS programming experience. * Experience with managing Lab Data, such as PK, PD, and Biomarkers. * Detail-oriented ...

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Medidata Rave Developer information

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How much do medidata rave developer jobs pay per hour?

As of Jun 24, 2026, the average hourly pay for medidata rave developer in the United States is $52.84, according to ZipRecruiter salary data. Most workers in this role earn between $40.38 and $64.66 per hour, depending on experience, location, and employer.

What are some common challenges faced by Medidata Rave Developers when customizing EDC studies, and how can they be addressed?

Medidata Rave Developers often encounter challenges related to balancing complex protocol requirements with system limitations, such as creating custom edit checks or integrating third-party data sources. Managing study amendments and maintaining data integrity during mid-study changes can also be demanding. These challenges can be addressed by thorough documentation, close collaboration with study teams and data managers, and leveraging Medidata community resources for best practices. Staying updated on the latest Medidata Rave releases and participating in regular training can also help developers efficiently handle evolving study needs.

What are the key skills and qualifications needed to thrive as a Medidata Rave Developer, and why are they important?

To thrive as a Medidata Rave Developer, you need a strong background in clinical data management, database programming, and familiarity with clinical trial processes, often supported by a bachelor's degree in life sciences, computer science, or a related field. Proficiency in Medidata Rave EDC, Rave Architect, and understanding of CDISC standards, along with certifications in Medidata Rave, are typically required. Attention to detail, problem-solving skills, and effective communication are essential soft skills for collaborating with clinical teams and ensuring data accuracy. These skills are crucial for building robust clinical trial databases that support regulatory compliance and reliable data collection in clinical research.

What is the difference between Medidata Rave Developer vs Clinical Data Coordinator?

AspectMedidata Rave DeveloperClinical Data Coordinator
Primary RoleDesigning, developing, and maintaining electronic data capture (EDC) systems using Medidata RaveManaging and overseeing clinical trial data collection, entry, and quality control
Required SkillsMedidata Rave platform expertise, database management, scripting, and programming skillsData management, clinical trial processes, attention to detail, and communication skills
Work EnvironmentClinical research organizations, pharmaceutical companies, CROsClinical sites, research organizations, pharmaceutical companies

While both roles are involved in clinical data management, Medidata Rave Developers focus on building and maintaining the electronic data capture systems, whereas Clinical Data Coordinators handle data entry, validation, and quality assurance during trials. Both roles are essential in the clinical research process but differ in technical focus and responsibilities.

What are Medidata Rave Developers?

Medidata Rave Developers are specialized professionals who design, build, and maintain electronic data capture (EDC) systems using Medidata Rave, a leading platform in clinical data management. They are responsible for creating study databases, designing electronic case report forms (eCRFs), programming edit checks, and ensuring compliance with regulatory standards. Their work enables clinical trial data to be collected, validated, and managed efficiently, supporting pharmaceutical and biotech companies in conducting successful clinical studies.
More about Medidata Rave Developer jobs
Infographic showing various Medidata Rave Developer job openings in the United States as of June 2026, with employment types broken down into 1% Internship, 2% Full Time, 1% Part Time, 2% Temporary, and 94% Contract. Highlights an 81% Physical, 5% Hybrid, and 14% Remote job distribution, with an average salary of $109,905 per year, or $52.8 per hour.
Clinical Data Manager

Clinical Data Manager

Encoded Therapeutics

South San Francisco, CA โ€ข On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Job description

Encoded Therapeutics Inc. is a biotechnology company advancing precision medicines for a broad range of genetic disorders. Our mission is to unlock new opportunities for viral gene therapy through genomics-driven discovery. We focus on delivering life-changing advances for individuals with genetic disorders not addressable with current approaches. For more information, please visit www.Encoded.com.

Position Details

We are seeking a collaborative, detail-oriented, and scientifically driven Clinical Data Manager to support the planning, execution, and oversight of clinical data management activities across our gene therapy clinical development programs. Reporting to the Senior Director of Clinical Data Management, this individual will partner cross-functionally with Clinical Operations, Biostatistics, Medical Monitoring, Regulatory Affairs, Pharmacovigilance, Quality, and external CROs/vendors to ensure delivery of high-quality, reliable, and inspection-ready clinical trial data.

The Clinical Data Manager will oversee data management activities across one or more clinical studies or workstreams, supporting study startup, database development, data cleaning, reconciliation, reporting, database lock, and regulatory submission readiness activities. The Clinical Data Manager will ensure the accuracy, consistency, completeness, and high quality of the clinical data.ย 

The ideal candidate is a proactive problem solver who thrives in a fast-paced biotech environment and is passionate about supporting transformative therapies for patients with serious diseases.

Responsibilities

  • Serve as the Clinical Data Manager for assigned studies and/or lead specific, specialized data management workstreams (e.g., manual data review, external vendor data management) across multiple studies within a clinical program
  • Participate in protocol and amendment reviews of assigned studies or program workstreams to ensure optimal CRF design and cross-study data standardization
  • Partner with Clinical and Biometrics to develop or contribute to comprehensive Data Management Plans and Data Review Plans, covering all aspects of data collection, processing, reconciliation, review, and archival for the assigned scope
  • Lead or support the design and build of the clinical databases and review tools to ensure they support clinical study objectives
  • Responsible for user acceptance testing (UAT) within assigned study scopes or workstreams, including authoring and/or executing scripts
  • Oversee or execute assigned aspects of data collection and review, which may include: monitoring data flow, performing discrepancy management, leading and participating in data review or reconciliation activities, and planning/facilitating database lock
  • Manage timelines for assigned CDM activities to support corporate and clinical program objectives.
  • Ensure complete, accurate and inspection-ready CDM documentation within the assigned scope
  • Ensure all CDM documentation are complete, accurate and inspection-ready state.
  • Act as team SME for key data systems and data streams, and process enhancement efforts
  • Contribute to program deliverable timeline creation
  • Performs additional duties as assigned

Requirements

  • BS/BA and/or MS degree Bachelor's degree or equivalent combination of education/experience in science or health-related field with 4 years of direct data management experience (Rare disease experience highly desirable)
  • Strong knowledge of CDM processes, EDC systems (Medrio and Medidata RAVE preferably), database programming, and quality management
  • Understanding of the MedDRA and WHODRUG coding processes.
  • Knowledgeable in GCP standards, CDISC standards (CDASH, SDTM, ADaM), FDA and ICH guidelines, and recommended CDM Best Practices
  • Outstanding problem-solving abilities and influencing/negotiation skills
  • Excellent interpersonal, communication, and leadership skills
  • Logical thinking, attention to detail and accuracy, good organizational skills, and problem-solving abilities
  • Ability to prioritize and adapt quickly to changing business conditions with a positive attitude
  • Willing to travel if required

Preferred Qualifications

  • Experience supporting gene therapy, rare disease, neurology, or cell therapy clinical programs.
  • Experience with electronic patient reported outcomes.
  • Experience with the review, reconciliation, and cleaning of neurodevelopmental, behavior, and motor assessments.
  • Experience operating with in-house data management as well as managing outsourced CRO/vendor data management models.
  • Familiarity with biomarker, genomic, imaging, longitudinal, or complex external datasets common within gene therapy development.
  • Experience supporting global clinical studies, regulatory inspections, and submission activities preferred.
  • Experience in an emerging biotechnology or growth-stage company environment preferred.
  • Knowledge of CDISC SDTM/ADaM principles and clinical data standards preferred.

Benefits

  • Comprehensive benefits package, including competitive employer premium contributions
  • Meaningful stock option grants
  • PTO, sick time, and holiday pay
  • Generous Parental Leave program
  • Pre-tax medical and dependent care programs
  • STD, LTD, Life and AD&D
  • Professional development opportunities
  • Team-building events
  • Fully stocked kitchen
  • Fitness center

Employees (and their families) may obtain medical, dental, vision and basic life insurance benefits through the company and enroll in our company's 401k plan. Employees will also accrue vacation time off and paid sick time off and may become eligible for paid parental leave. Employees will also enjoy designated paid holidays throughout the calendar year.

Encoded is an Equal Opportunity Employer and prohibits discrimination and harassment of any kind. Encoded is committed to the principle of equal employment opportunity for all employees and to providing employees with a work environment free of discrimination and harassment. All employment decisions at Encoded are based on business needs, job requirements and individual qualifications, without regard to race, religion or belief, color, national origin, gender, status as a protected veteran, status as an individual with a disability, or any other status protected by the laws or regulations in the location in which we operate. Encoded will not tolerate discrimination or harassment based on any of these characteristics. Encoded encourages applicants of all ages.

If you need assistance or an accommodation due to a disability, you may call us at +1 650-491-0272.

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