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Clinical Data Manager Medidata Rave Jobs (NOW HIRING)

MapLight Therapeutics

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 ...

CYNET SYSTEMS

Clinical Data Manager

Sunnyvale, CA · On-site

$70 - $75/hr

Clinical data review and listing experience (Preferably Medrio, Medidata Rave). * Excellent understanding of data administration and management functions (collection, analysis, data review process ...

Vor Bio

Senior Data Manager

Boston, MA · On-site

... clinical data management systems and/or EDC products e.g. Medidata Rave. Must have Medidata RAVE ... experience. * Strong project management; exhibits expertise in metrics analysis and reporting ...

Cytel

Senior Database Developer

Cambridge, MA · On-site +1

... Data Management, Statistical Programming, Clinical Operations, and external partners. * Lead and oversee EDC database builds in Medidata Rave, including CRF design, edit checks, derivations, code ...

Cytel

Senior Database Developer

Cambridge, MA · On-site +1

... Data Management, Statistical Programming, Clinical Operations, and external partners. * Lead and oversee EDC database builds in Medidata Rave, including CRF design, edit checks, derivations, code ...

Atorus Research

Sr Medidata RAVE Programmer

Sr Medidata RAVE Programmer Remote from anywhere in the U.S. or Canada Contract/Corp to Corp JOB ... clinical data management practices PREFERRED SKILLS • Good organizational skills • Good ...

Clinovo

Senior Data Manager

Palo Alto, CA · On-site

$130K/yr

Senior Clinical Data Manager Role Overview The Senior Clinical Data Manager will play a critical ... Strong familiarity with clinical data systems such as Medidata Rave, Oracle Clinical, and/or Veeva ...

CTI

Clinical Programmer

Covington, KY · On-site +1

... such as Medidata Rave or OmniComm TrialMaster, program validation checks, and ensure all data ... Work with lead CP or Study Clinical Data Manager to implement system edits on built entry screens

IQVIA

Lead Clinical Data Manager (Remote)

New York, NY · Remote

$68K - $217K/yr

Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider ... Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP ...

IQVIA

Lead Clinical Data Manager (Remote)

Raleigh, NC · Remote

$68K - $217K/yr

Hiring multiple Clinical Data Management (CDM) Leads across our FSP (Functional Service Provider ... Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP ...

Systimmune

EDC Programmer

Redmond, WA · On-site

$100K - $150K/yr

The EDC Programmer (EDCP) is a critical technical role responsible for building, configuring, and maintaining clinical trial databases in Medidata Rave. Sitting in the Clinical Data Management (CDM ...

CTI

Clinical Programmer

Covington, KY · On-site +1

... such as Medidata Rave or OmniComm TrialMaster, program validation checks, and ensure all data ... Work with lead CP or Study Clinical Data Manager to implement system edits on built entry screens

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How much do clinical data manager medidata rave jobs pay per hour?

As of Jun 9, 2026, the average hourly pay for clinical data manager medidata rave in the United States is $57.17, according to ZipRecruiter salary data. Most workers in this role earn between $45.19 and $68.03 per hour, depending on experience, location, and employer.
Infographic showing various Clinical Data Manager Medidata Rave job openings in the United States as of May 2026, with employment types broken down into 83% Full Time, 11% Part Time, and 6% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $118,909 per year, or $57.2 per hour.

Clinical Data Manager

MapLight Therapeutics

Burlington, MA • Hybrid

Other

Posted 21 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.

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