ZipRecruiter

Log In

1

Clinical Trial Data Manager Jobs (NOW HIRING)

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

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 ...

Kymera Therapeutics

Clinical Trial Manager

Watertown, MA · On-site

$115K - $200K/yr

Our goals are shared, our decisions data-driven and our camaraderie genuine. * BELONG : We ... Responsible for management of vendors to support clinical trial execution * Plan, execute, and lead ...

Jobgether

You will oversee the full data management lifecycle, ensuring the quality, accuracy, and integrity of clinical trial data from study start-up through closeout. Working within a collaborative and ...

Viking Therapeutics

Clinical Data Manager

San Diego, CA · On-site

$110K - $120K/yr

Ensure the development of high-quality study documentation from CROs for clinical trial data collection, handling, processing, quality control, and archival, including Data Management Plans (DMP)

Abbott

MN · On-site

$45 - $47/hr

Clinical Data Manager Location: Maple Grove, MN Duration: 7 Months 100% Onsite Summary: The ... Review of study data to detect anticipated and unanticipated issues related to trial data ...

Abbott

Clinical Data Manager

Maple Grove, MN · On-site

$45 - $47/hr

Clinical Data Manager Location: Maple Grove, MN Duration: 7 Months 100% Onsite Summary: The ... Review of study data to detect anticipated and unanticipated issues related to trial data ...

next page

Showing results 1-20

All JobsClinical Trial Data JobsClinical Trial Data Manager Jobs

Clinical Trial Data Manager information

See salary details

$28

$62

$96

How much do clinical trial data manager jobs pay per hour?

As of Aug 5, 2026, the average hourly pay for clinical trial data manager in the United States is $62.52, according to ZipRecruiter salary data. Most workers in this role earn between $50.72 and $70.43 per hour, depending on experience, location, and employer.

What is the difference between Clinical Trial Data Manager vs Clinical Research Coordinator?

AspectClinical Trial Data ManagerClinical Research Coordinator
Primary RoleManages and oversees clinical trial data collection, validation, and analysisCoordinates daily trial activities, patient recruitment, and site management
Required SkillsData management, database systems, regulatory compliancePatient interaction, study protocol adherence, site coordination
Work EnvironmentData management teams, clinical trial offices, CROsClinical sites, hospitals, research facilities
Common CertificationsCDMP, SAS certifications often preferredGCP certification often required

While both roles are essential in clinical trials, the Clinical Trial Data Manager focuses on data integrity and analysis, whereas the Clinical Research Coordinator handles site operations and patient interactions. Understanding these differences helps in choosing the right career path or job search focus within clinical research.

More about Clinical Trial Data Manager jobs
What cities are hiring for Clinical Trial Data Manager jobs? Cities with the most Clinical Trial Data Manager job openings:
What states have the most Clinical Trial Data Manager jobs? States with the most job openings for Clinical Trial Data Manager jobs include:
What job categories do people searching Clinical Trial Data Manager jobs look for? The top searched job categories for Clinical Trial Data Manager jobs are:
Clinical Trial Data Manager jobs near you
Infographic showing various Clinical Trial Data Manager job openings in the United States as of July 2026, with employment types broken down into 2% As Needed, 73% Full Time, 17% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $130,034 per year, or $62.5 per hour.

Clinical Data Manager

MapLight Therapeutics

Burlington, MA • Hybrid

Other

Re-posted 18 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.

Apply