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Internship Clinical Programmer Medidata Rave Jobs

Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ... clinical systems and data administration * Must be organized, an effective written and oral ...

Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ... clinical systems and data administration * Must be organized, an effective written and oral ...

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for ... Oversee Medidata Rave electronic data capture (EDC) system setup, configuration, user management ...

Biotech Specialist - AI Trainer

Houston, TX · On-site +1

$1.1K - $1.4K/wk

Build a realistic digital workspace using tools like Medidata Rave , Oracle Clinical One , Schrödinger Suite , and Benchling . Include study protocols, IND/NDA/BLA drafts, and lab notebooks.

Data Architect

Austin, TX · On-site

$100 - $130/hr

... Medidata Rave, Veeva, Oracle Clinical One, and custom sponsor environments. Your work directly ... You will partner with clinical operations, QC analysts, integration engineers, and AI/automation ...

Senior Clinical Research Coordinator

La Jolla, CA · On-site

$25.50 - $33.75/hr

The Senior Clinical Research Coordinator (CRC) is the site-level owner for the onboarding and ... Enter and verify data in electronic data capture (EDC) systems (e.g., REDCap, Medidata Rave) with ...

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Internship Clinical Programmer Medidata Rave information

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How much do internship clinical programmer medidata rave jobs pay per hour?

As of Aug 11, 2026, the average hourly pay for internship clinical programmer medidata rave 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.
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Infographic showing various Internship Clinical Programmer Medidata Rave job openings in the United States as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.

Clinical Data Manager

MapLight Therapeutics

Burlington, MA • Hybrid

Full-time

Re-posted 24 days ago


Job description

What You'll Do:

We are seeking a highly skilled and motivated Clinical Data Manager to join our Clinical Data Management team. Reporting to the Associate Director, the Clinical Data Manager, will play a pivotal role in ensuring the integrity, accuracy, and completeness of clinical trial data, contributing to the successful development and regulatory approval of our products.

 Responsibilities:

  • Manage and lead all aspects of clinical trial data management activities from study start-up to database lock.
  • Develop and implement data management plans, data validation plans, edit check plans and data entry guidelines in compliance with regulatory standards and company SOPs.
  • Collaborate with cross-functional teams including Clinical Operations, Biostatistics, and Regulatory Affairs to ensure data quality and integrity throughout the trial lifecycle.
  • Oversee Medidata Rave electronic data capture (EDC) system setup, configuration, user management, coding and data extracts.
  • Perform data cleaning, discrepancy management, SAE and vendor integration reconciliation activities to ensure timely database lock.
  • Conduct periodic data reviews and generate weekly data quality metrics to identify trends and outliers.
  • Identify Protocol Deviations
  • Produce medical monitor, coding listings and ad hoc listings for team review (Jreview, SAS, Business Objects).
  • Participate in the development and review of clinical study protocols, case report forms (CRFs), and clinical trial documentation.
  • Provide support for regulatory submissions, audits, and inspections related to clinical trial data management.
  • Stay current with industry standards, best practices, and regulatory requirements related to clinical data management.

Qualifications:

  • Bachelor's degree in life sciences, computer science, or a related field. Advanced degree preferred.
  • Minimum of 5 years of experience in clinical data management within the pharmaceutical or biotechnology industry.
  • Proficiency in Medidata Rave electronic data capture (EDC) system..
  • Strong understanding of Good Clinical Practice (GCP) guidelines, regulatory requirements (e.g., FDA, EMA), and industry standards (e.g., CDISC).
  • Excellent communication, organizational, and problem-solving skills.
  • Ability to work effectively in a fast-paced, cross-functional team environment.
  • Attention to detail and commitment to data quality and integrity.

Location: This is a hybrid position with three days per week onsite at our office in Burlington, MA or Redwood City, CA.

MapLight does not accept unsolicited resumes from recruiters, staffing agencies, or search firms.