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Clinical Data Manager Jobs (NOW HIRING)

Collabera

Clinical Data Manager

Irvine, CA · On-site

Clinical Data Manager Location: Irvine, CA USA 92618 Duration: 12 months (Strong Possibility of Extension) Employment Type: W2 Contingent Worker SUMMARY OF POSITION: As a key member of the Global ...

TScan Therapeutics

Clinical Data Manager

Waltham, MA

$130K - $150K/yr

Reporting to our Senior Clinical Data Manager the ideal candidate should have relevant experience in leading internal and external data management activities in oncology clinical studies and enjoy ...

TScan Therapeutics

Clinical Data Manager

Waltham, MA

$130K - $150K/yr

Reporting to our Senior Clinical Data Manager the ideal candidate should have relevant experience in leading internal and external data management activities in oncology clinical studies and enjoy ...

TScan Therapeutics

Clinical Data Manager

Waltham, MA · On-site

$130K - $150K/yr

Reporting to our Senior Clinical Data Manager the ideal candidate should have relevant experience in leading internal and external data management activities in oncology clinical studies and enjoy ...

Viz.ai

Clinical Data Manager

$127K - $182K/yr

This position plays a critical role in driving Viz's Evidence Generation strategy by managing the data life-cycle for clinical research and quality improvement studies. This role requires expertise ...

SystImmune, Inc

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams, external partners, and vendors to design, configure, and test clinical database systems, conduct data ...

Medix

Clinical Data Manager

Menlo Park, CA · On-site

$42 - $50/hr

Enter and update study data using the Clinical Trial Management System. * Provide training and guidance to lower-level coordinators. * Participate in the interview and selection process of new ...

asrcfh

Clinical Data Manager 2

Reston, VA · On-site

Agile Decision Sciences LLC is looking for a Clinical Data Manager to support the growing team. Responsibilities : * Manage the delivery of high-quality data from project start-up and planning to ...

asrcfh

Clinical Data Manager 2

Reston, VA

Agile Decision Sciences LLC is looking for a Clinical Data Manager to support the growing team. Responsibilities : * Manage the delivery of high-quality data from project start-up and planning to ...

Iterative Health

Clinical Data Manager

Manhattan, NY · On-site

$97K - $120K/yr

Clinical Data Manager Cambridge, Massachusetts, United States, New York, New York, United States Iterative Health is a healthcare technology and services company powering the acceleration of clinical ...

New

Pharmaron

Senior Clinical Data Manager

Somerset, NJ · On-site

$90K - $100K/yr

Position: Senior Clinical Data Manager FLSA Status: Exempt Location: Onsite (Somerset, New Jersey) Salary: $90,000 to $100,000 About Pharmaron Pharmaron is a global CRO (Contract Research ...

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Clinical Data Manager information

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How much do clinical data manager jobs pay per hour?

As of Jun 20, 2026, the average hourly pay for clinical data manager 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.

What are some common challenges Clinical Data Managers face when working on multi-site clinical trials?

Clinical Data Managers often encounter challenges such as ensuring data consistency across different sites, managing large volumes of complex data, and coordinating with site staff to resolve discrepancies. They must also stay up-to-date with regulatory requirements and ensure timely data cleaning and database lock. Effective communication and strong organizational skills are essential to navigate these complexities and maintain high data quality throughout the study.

What jobs pay 2000 a day?

Clinical Data Managers typically do not earn $2,000 a day; such high daily rates are more common in specialized consulting, executive roles, or freelance positions in fields like finance or law. Some highly experienced professionals or contractors in niche areas may reach this level with advanced skills and certifications, but it is uncommon for standard roles. Most high-paying jobs at this level require extensive experience, advanced degrees, or independent consulting arrangements.

What are the key skills and qualifications needed to thrive as a Clinical Data Manager, and why are they important?

To thrive as a Clinical Data Manager, you need a solid understanding of clinical research processes, data management principles, and a degree in life sciences, computer science, or related fields. Expertise with clinical data management systems (CDMS), electronic data capture (EDC) tools, and familiarity with regulatory standards like CDISC and GCP are typically required. Attention to detail, problem-solving abilities, and effective communication distinguish top performers in this role. These skills ensure accurate, compliant data handling and seamless collaboration across clinical research teams, which are critical for successful clinical trial outcomes.

What does a Clinical Data Manager do?

A Clinical Data Manager is responsible for collecting, validating, and managing data from clinical trials to ensure its accuracy, integrity, and compliance with regulatory standards. They design data collection systems, oversee database development, and collaborate with clinical research teams to resolve data discrepancies. By ensuring high-quality data, Clinical Data Managers play a vital role in the success of clinical trials and the development of new medical treatments.

Is CRA an entry-level job?

A Clinical Research Associate (CRA) is typically not an entry-level position; it usually requires prior experience in clinical research, monitoring, or related fields. Entry-level roles in clinical research often include Clinical Trial Assistants or Coordinators, while CRAs often need knowledge of Good Clinical Practice (GCP) and relevant certifications. However, some companies may offer junior CRA roles for candidates with limited experience who demonstrate strong foundational skills.

What Does a Clinical Data Manager Do?

A clinical data manager handles all the data needs of clinical trials for biotechnology and pharmaceutical companies. As a clinical data manager, your responsibilities include the research and storage of data related to clinical trials and programs. Your job duties are to collect, process, and analyze data. You must routinely evaluate your data collection and analysis processes to ensure that results are accurate and valid. You must also ensure that your work is in compliance with ethical research standards and regulations from organizations like the Food and Drug Administration (FDA).

What is a Clinical Data Manager?

A Clinical Data Manager is responsible for designing, managing, and ensuring the accuracy and integrity of data collected during clinical trials. They work with electronic data capture systems, develop data management plans, and collaborate with research teams to ensure compliance with regulatory standards. Strong attention to detail and knowledge of data management tools like SQL or SAS are essential in this role.

What is the role of a Clinical Data Manager?

A Clinical Data Manager is responsible for designing, implementing, and maintaining systems to collect, manage, and ensure the quality of clinical trial data. They oversee data validation, perform data cleaning, and collaborate with study teams to ensure accurate and compliant data collection using tools like electronic data capture (EDC) systems. Their role is essential for the integrity and reliability of clinical trial results.
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Clinical Data Manager jobs near you
Clinical Data Manager

Clinical Data Manager

Pharmavise Corporation

Indianapolis, IN • Remote

Contractor

Medical, PTO

Posted 29 days ago

Job description

This is a remote position.

The Clinical Data Manager (CDM) is responsible for the oversight, integrity, and quality of clinical trial data from collection through database lock. The CDM ensures that data is accurate, consistent, and meets regulatory and protocol-specific requirements. This role collaborates closely with cross-functional teams, including Clinical Operations, Biostatistics, Medical Writing, and Regulatory Affairs, to support timely and compliant study execution. 
Key Responsibilities: 
Design and review Case Report Forms (CRFs) and Electronic Data Capture (EDC) systems to ensure accurate and complete data capture aligned with the study protocol. 
Develop and maintain data management plans (DMPs), data validation specifications, and CRF completion guidelines. 
Oversee data cleaning activities, including the generation, review, and resolution of data queries in collaboration with clinical sites and study teams. 
Perform ongoing data reviews to identify trends, inconsistencies, or protocol deviations. 
Ensure adherence to data standards (e.g., CDISC, SDTM) and regulatory requirements (e.g., FDA, ICH-GCP). 
Manage database lock activities and contribute to the preparation of clinical study reports (CSRs). 
Serve as the primary point of contact for data management vendors and oversee their deliverables. 
Participate in study team meetings and provide status updates related to data quality and timelines. 
Support audit readiness and participate in regulatory inspections when required. 
Minimum Qualifications: 
Bachelor’s degree in Life Sciences, Computer Science, Health Informatics, or related field. Advanced degree is a plus. 
Minimum of 3–5 years of experience in clinical data management within a pharmaceutical, biotech, or CRO environment. 
Proficiency in EDC platforms (e.g., Medidata Rave, Oracle InForm, Veeva, REDCap). 
Strong understanding of ICH-GCP, FDA regulations, and CDISC standards. 
Experience with data listings, query management, edit check programming, and coding dictionaries (e.g., MedDRA, WHODrug). 
Excellent organizational, analytical, and problem-solving skills. 
Strong communication and collaboration skills across cross-functional teams. 
Experience working on global, multi-site clinical trials preferred. 
In addition to a dynamic and collaborative work environment, we offer a comprehensive benefits package to support our employees\' well-being. Our benefits include paid holidays, Paid Time Off (PTO) policy, and medical insurance to ensure our team members have the flexibility and coverage they need. We believe in fostering a healthy work-life balance while providing the necessary support for professional and personal growth. 
Be part of our network of Subject Matter Experts.
E-Verify Participation:  
Pharmavise Consulting Corporation participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, Pharmavise is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue. For more information on E-Verify, please contact DHS at 888-897-7781 or through their website at dhs.gov/e-verify. 

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