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Home Based Clinical Data Manager Jobs (NOW HIRING)

Faeth Therapeutics

Clinical Data Manager

San Francisco, CA · On-site

$125K - $175K/yr

Faeth Therapeutics is seeking an experienced Clinical Data Manager to support clinical data ... vary based on experience, qualifications and location) Working at Faeth Benefits: * Competitive ...

asrcfh

Clinical Data Manager

Reston, VA · On-site

Agile Decision Sciences LLC is looking for a Clinical Data Manager 4 to support our growing Center for International Blood & Marrow Transplant Research (CIBMTR) team Responsibilities : * Manage the ...

Pharmaron

Clinical Data Manager

Somerset, NJ · On-site

$60K - $75K/yr

Identify the work scope of the study and create a study timeline based on the clinical protocol. * Participate in internal/external functional meetings. * Oversight of all data management tasks ...

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 ... Pay Range: $130,000-$150,000 Pay Transparency TScan Therapeutics' pay ranges are established based ...

Intuitive

Clinical Data Manager

Sunnyvale, CA

Provide clinical data management support for study operations and analysis groups including the ... Compensation will be based primarily on the job level at which the role is filled and the candidate ...

Systimmune

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 ... Actual compensation will be based on a variety of factors, including but not limited to a candidate ...

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 ... Eligibility for health benefits is based on verifying that an average of 30 hours per week during ...

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 ...

Cooper Companies

Lead Clinical Data Manager

San Ramon, CA · Hybrid

$164K - $219K/yr

Leads all aspects of clinical data management activities from study initiation through database lock and study closeout. Develops, optimizes and controls data management system, including external ...

Cytel

Principal Clinical Data Manager

Cambridge, MA · Remote

Principal Clinical Data Manager United States (Remote) Responsibilities - Responsible for vendor oversight activities across global development programs. - Represents data management function on the ...

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Home Based Clinical Data Manager information

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How much do home based clinical data manager jobs pay per hour?

As of Jul 12, 2026, the average hourly pay for home based 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.

Which is better, CDM or SAS?

For a Home Based Clinical Data Manager, SAS is a widely used software for data analysis and management in clinical trials, offering robust statistical capabilities. CDM (Clinical Data Management) refers to the overall process and roles involved in managing clinical data, often utilizing tools like SAS, SQL, or electronic data capture systems. The choice depends on the specific job requirements, with SAS skills being highly valued for data analysis tasks within clinical data management roles.

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

To thrive as a Home Based Clinical Data Manager, you need a strong background in life sciences or related fields, along with experience in clinical data management and knowledge of regulatory requirements. Familiarity with data management systems like Medidata Rave, Oracle Clinical, and understanding of CDISC standards, as well as certifications such as CCDM, are highly valuable. Attention to detail, strong organizational skills, and effective remote communication are essential soft skills in this role. These skills and qualifications ensure data integrity, regulatory compliance, and efficient collaboration in decentralized clinical research environments.

What is the difference between Home Based Clinical Data Manager vs Clinical Data Coordinator?

AspectHome Based Clinical Data ManagerClinical Data Coordinator
CredentialsBachelor's degree in health sciences, life sciences, or related field; experience with clinical data systemsBachelor's degree; familiarity with data entry and management
Work EnvironmentRemote, home-based setting, often with flexible hoursTypically office-based or site-based, sometimes remote
Employer & IndustryPharmaceutical companies, CROs, research institutionsHospitals, clinics, research organizations
Search & Comparison IntentUnderstanding remote data management roles in clinical researchLearning about data entry and coordination in clinical trials

The Home Based Clinical Data Manager primarily oversees clinical data remotely, ensuring data quality and compliance, while the Clinical Data Coordinator handles data entry and basic management tasks on-site or in-office. Both roles require similar educational backgrounds but differ mainly in work setting and scope of responsibilities.

How to get a job as a Clinical Data Manager?

To become a Clinical Data Manager, candidates typically need a bachelor's degree in health sciences, life sciences, or a related field, along with experience in clinical research or data management. Proficiency in data management tools like EDC systems and knowledge of regulatory standards such as GCP and FDA guidelines are important. Certifications like CDMP can enhance job prospects, and strong attention to detail and analytical skills are essential for success in this role.

What is a Home Based Clinical Data Manager?

A Home Based Clinical Data Manager is a professional responsible for collecting, managing, and ensuring the quality of clinical trial data while working remotely from home. They coordinate with clinical research teams, review data for accuracy, and ensure regulatory compliance throughout the clinical study process. This role often involves using specialized software to manage large datasets, resolve discrepancies, and prepare data for analysis and submission to regulatory authorities.

How much does a Pfizer Clinical Data Manager make?

A Clinical Data Manager at Pfizer typically earns between $80,000 and $120,000 annually, depending on experience, location, and level of responsibility. The role requires proficiency with data management tools and adherence to regulatory standards, often involving collaboration with cross-functional teams.

How can I make 2000 a week working from home?

A Home Based Clinical Data Manager can increase earnings by taking on multiple projects, working overtime, or securing higher-paying contracts that require advanced skills and certifications. Building expertise in data management tools and maintaining a strong professional network can also help access better opportunities to reach a weekly income of $2000.

What are some common challenges faced by home-based Clinical Data Managers, and how can they be addressed?

Home-based Clinical Data Managers often face challenges such as maintaining clear communication with cross-functional teams, staying updated on project changes, and managing data security remotely. To address these, it’s important to leverage collaboration tools like secure messaging platforms and project management software, establish regular check-ins with colleagues, and strictly adhere to data privacy protocols. Additionally, setting up a dedicated and secure workspace at home can help ensure focus and compliance with regulatory standards.
What cities are hiring for Home Based Clinical Data Manager jobs? Cities with the most Home Based Clinical Data Manager job openings:
What are the most commonly searched types of Clinical Data Manager jobs? The most popular types of Clinical Data Manager jobs are:
What states have the most Home Based Clinical Data Manager jobs? States with the most job openings for Home Based Clinical Data Manager jobs include:
Home Based Clinical Data Manager jobs near you

Principal Data Manager I

Everest Clinical Research

Bridgewater, NJ • On-site, Remote

$130K - $165K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 26 days ago

Job description

Everest Clinical Research ("Everest") is a full-service contract research organization (CRO) providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries. We serve some of the best-known companies and work with many of the most advanced drugs, biologics, and medical devices in development today.
Everest has been an independent CRO since 2004 with a strong foundation as a statistical and data management center of excellence. Building on this foundation, Everest has successfully developed and established itself as a full-service CRO. Everest's headquarters are located in Markham (Greater Toronto Area), Ontario, Canada with additional sites in Bridgewater (Greater New York City Area), New Jersey, USA, Shanghai (Pudong Zhangjiang New District), China and Taipei, Taiwan.
Everest is known in the industry for its high quality deliverables, superior customer service, and flexibility in meeting clients' needs. A dynamic organization with an entrepreneurial origin, Everest continues to experience exceptional growth and great success.
Quality is our backbone, customer-focus is our tradition, flexibility is our strength...that's us...that's Everest.
To drive continued success in this exciting clinical research field, we are seeking committed, skilled, and customer-focused individuals to join our winning team as Principal Clinical Data Manager for our Bridgewater, New Jersey, USA on-site location, or remotely from a home-based office anywhere in the USA in accordance with our Work from Home policy.
Key Accountabilities:
  1. Act as the primary contact person for communication and discussion of topics related to data management timelines and deliverables; requests for out-of-scope tasks; and first line contact for technical or procedural issues.
  2. Perform hands-on data management tasks including, but not limited to, writing database design specifications, test plans for user acceptance testing (UAT), and data transfer specifications. When these tasks are assigned to Data Management support team members, the Principal Clinical Data Manager is responsible for review or to provide data management oversight and approvals for the task performed to ensure quality deliverable, including review of UAT plans to ensure accuracy and consistency among projects. Facilitate and participate in UAT, as necessary.
  3. Review data, issue queries, and resolve queries from various data sources (e.g., medical coding, medical history, adverse events, procedures and medicinal products, and external data). Assist other Clinical Research Organizations, Sponsor, or Investigative Sites with resolving queries.
  4. Perform third party non-Case Report Form data management activities.
  5. Plan, manage, and perform data processing and data management activities for assigned projects to ensure tasks are performed in a timely manner and in compliance with trial Sponsors' requirements.
  6. Accurately and efficiently validate electronically captured data. Lead efforts in writing clear queries on missing data and data points failing pre-defined range checks and/or logical checks.
  7. Validate and disseminate real-time study monitoring reports to Sponsor and internal team members.
  8. Review database edit check specifications for assigned studies. Lead efforts in developing and maintaining standard database validation checks for common modules as well as for therapeutic/drug area specific modules.
  9. Perform training on the electronic data capture (EDC) system, dataflow, and quality control (QC) processes to clinical trial personnel.
  10. Participate in project kick off meetings, investigators meetings, and regular project management team meetings.
  11. Perform study-level resource planning and management, including the review of team members' timesheet reports.
  12. Manage the process of database modifications (after go-live) due to protocol amendments or study needs.
  13. Develop and maintain the Data Management Plan (DMP). Document deviations from the DMP.
  14. Assist in development and implementation of clinical data standards, training standards, project management, and data management technologies.
  15. Develop and maintain the Data Quality Review Plan (DQRP). Coordinate with programmers to complete the programming and validation of the listings and summary tables as specified in the DQRP.
  16. Assist in the development of project bids, billing, tracking of out-of-scope tasks, and participate in bid defense meetings.
  17. Perform project tracking and maintain project milestones and timelines. Report and resolve any issues with defined timelines and deliverables to the next line of management.
  18. Promote effective project management practices. Review and assess timesheet summary reports for assigned projects.
  19. Follow up on regulatory requirements, industry trends, benchmarks, and best working practices in data management by reading and participating in relevant training and/or association activities.
  20. Participate in and contribute to CDM departmental improvement initiatives.
  21. Define and monitor clinical trial data flow and QC processes in accordance with corporate Standard Operating Procedures, Good Working Practices, and departmental guidelines.
  22. Provide training to study site and Sponsor personnel on data entry and review (electronic data capture studies), data flow, and QC processes.
  23. Cooperate and assist the Quality Assurance (QA) department with QA audits on assigned databases.
  24. Ensure project team maintains and prepares final archival of data management documentation relevant to the assigned clinical trials and assist the corporate archivist in assembling and archiving such documentation.

Qualifications and Experience:
  1. M.Sc. or B.Sc. in a related field.
  2. Ten (10) years of related experience.
  3. Demonstrated an in-depth understanding of clinical trial data management concepts, processes and procedures, relevant issues related to or impacting clinical data management, as well as pharmaceutical clinical trial regulations, industry guidance, conventions and standards.
  4. Demonstrated leadership ability to effectively manage clinical trial data management activities and integrate them with the entire clinical trial operation.
  5. Must communicate effectively, orally and in writing, with personnel on all professional and administrative levels.
  6. Excellent presentation skills and the ability to build relationships with both internal and external clients.
  7. Demonstrated ability to effectively organize and integrate the activities of information processing.
  8. Must be well organized, able to work independently, and manage multiple projects/tasks appropriately.
  9. Demonstrated knowledge of Data Management processes and data flow with the skill to ensure quality delivery.

Benefits & Compensation:
We offer a robust benefits package to support your health, well-being, and growth, including medical, dental, and vision coverage, life & AD&D insurance, short- and long-term disability, tuition reimbursement, fitness reimbursement, employee assistance program (EAP), a 401(k) retirement / pension plan, generous paid time off and sick leave, and the opportunity to earn a performance based bonus.
Estimated Salary Range: $130,000 - $165,000.
To find out more about Everest Clinical Research and to review other opportunities, please visit our website at www.everestclinical.com
We thank all interested applicants, however, only those selected for an interview will be contacted.
Everest is committed to upholding the principles of dignity, independence, integration, and equal opportunity. We welcome and encourage applications from people with disabilities, and upon request we will provide accommodations for candidates participating in any part of our recruitment and selection process.
#LI-Remote
#LI-KD1
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws. For further information, please review the Know Your Rights notice from the Department of Labor.

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