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Clinical Data Validation Jobs (NOW HIRING)

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for ... Develop and implement data management plans, data validation plans, edit check plans and data entry ...

FUTRUE

$79.65 - $113.79/hr

Du entwickelst und reviewst Datenmanagementpläne, Data-Validation-Pläne, Edit-Check ... EDC-Systeme wie Medidata Rave, Oracle Clinical, Veeva EDC, Castor EDC oder vergleichbaren ...

New

Vertanical

$90 - $120/hr

You will develop and review Data Management Plans, Data Validation Plans, edit check specifications ... You will ensure the reconciliation of the clinical database with safety and laboratory databases.

New

Socket.dev

Director, Clinical Data Management

Bedford, MA · On-site

$225 - $244/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Oversee the User Acceptance Testing (UAT) by CRO and Coordinating UAT of eCRF build and validation ... Ensure clinical data within EDC is of high quality to support lock/unlock and freeze/unfreeze as ...

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Clinical Data Validation information

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How much do clinical data validation jobs pay per hour?

As of Aug 19, 2026, the average hourly pay for clinical data validation in the United States is $39.26, according to ZipRecruiter salary data. Most workers in this role earn between $21.63 and $51.92 per hour, depending on experience, location, and employer.

What is clinical data validation?

A Clinical Data Validation job involves verifying and ensuring the accuracy, consistency, and integrity of clinical trial data. Professionals in this role check data for errors, discrepancies, and adherence to regulatory standards. They work closely with data management teams, using various validation tools and programming techniques to clean and validate data. This process ensures that clinical trial results are reliable and meet compliance requirements set by agencies like the FDA or EMA.

What does clinical data validation do?

In a Clinical Data Validation role, your daily tasks often include reviewing clinical trial data for accuracy and completeness, identifying and resolving discrepancies, and ensuring compliance with regulatory standards. You may work closely with data managers, biostatisticians, and clinical teams to address data queries and support ongoing data cleaning activities. Additionally, you’ll assist with the development and implementation of data validation plans, perform system checks, and contribute to the preparation of final study databases for analysis. These responsibilities require a high level of precision and a collaborative mindset, as quality data is crucial for the success of clinical research projects.

What are the key skills and qualifications needed to thrive in clinical data validation?

To excel in Clinical Data Validation, a strong background in clinical research, data management, and attention to detail is crucial, often supported by a degree in life sciences or a related field. Familiarity with data validation software, electronic data capture (EDC) systems, and knowledge of regulatory compliance guidelines such as CDISC and GCP are typically required. Excellent analytical thinking, problem-solving skills, and clear communication are vital for collaborating with cross-functional teams. These competencies ensure the accuracy and reliability of clinical trial data, which is essential for regulatory approvals and successful study outcomes.

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Clinical Data Validation jobs near you
Infographic showing various Clinical Data Validation job openings in the United States as of August 2026, with employment types broken down into 87% Full Time, 3% Part Time, and 10% Contract. Highlights an 97% In-person, and 3% Remote job distribution, with an average salary of $81,651 per year, or $39.3 per hour.

Clinical Data Manager

MapLight Therapeutics

Burlington, MA • On-site

$145K - $160K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago

Job description

Who We Are: MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for central nervous system disorders. We combine cutting-edge technologies including optogenetics, in vivo physiology, and spatial transcriptomics to identify novel drug targets and develop effective therapies to address psychiatric symptoms.
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.
Compensation for this role may vary within the above range based on many factors including geographic location, candidate experience, and skills. Additional compensation/benefits include annual bonus opportunity, medical, dental, vision, life and AD&D, short term and long term disability, 401(K) plan with match, stock options, flexible non-accrual paid time off, and parental leave.
Salary Range
$145,000-$160,000 USD
EEOC Statement: MapLight Therapeutics is an equal opportunity employer, and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, sexual orientation, gender identity, disability status, protected veteran status, or any other characteristic protected by law.

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