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Weekend Medidata Rave Programmer Jobs (NOW HIRING)

Actalent

Clinical Research Nurse

Philadelphia, PA · Hybrid

$40 - $45/hr

Experience with electronic data capture (EDC) systems such as Inform and MediData Rave. * Strong ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

SystImmune, Inc

Clinical Data Associate

Redmond, WA · 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 ...

SystImmune, Inc

Clinical Data Manager

Redmond, WA · 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 ...

Everest Clinical Research

Clinical Database Designer I

$50K - $90K/yr

One year clinical database design experience, such as developing clinical databases in DFdiscover, InForm, Medidata Rave, Clinical One, and/or other EDC systems. * Software programming experience ...

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As of Jun 20, 2026, the average hourly pay for weekend medidata rave programmer in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $51.44 per hour, depending on experience, location, and employer.
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Clinical Data Manager

Clinical Data Manager

Encoded Therapeutics

South San Francisco, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 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.
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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