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Clinical Data Manager Jobs (NOW HIRING)

EDETEK

Clinical Data Manager

The Clinical Data Manager (CDM) handles project management documentation, clinical data management activities, and system implementations for EDETEK's eClinical, and may be assigned work on other ...

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 ...

New

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 ...

New

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

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 ...

Sumitomo Pharma

Clinical Data Manager

$130K - $163K/yr

Execute and manage all in house clinical data management activities for assigned oncology trials in accordance with ICH/GCP, regulatory requirements, and internal SOPs. * Support and contribute to ...

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 management activities across two active clinical trials. This individual will play a critical role in ...

Faeth Therapeutics

Clinical Data Manager

San Francisco, CA · Remote

$125K - $175K/yr

Faeth Therapeutics is seeking an experienced Clinical Data Manager to support clinical data management activities across two active clinical trials. This individual will play a critical role in ...

ASRC Federal Holding

Clinical Data Manager

Reston, VA · On-site

Manage patient protocol information and review protocol and incorporate protocol-specific guidelines into the review of clinical trial data on several projects simultaneously * Contribute to the ...

Pharmaron

Clinical Data Manager

Somerset, NJ · On-site

$60K - $75K/yr

Clinical Data Manager FLSA Status: Exempt Location: Onsite (Somerset, New Jersey) Salary: $60,000 - $75,000 Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech ...

Pharmaron

Clinical Data Manager

Somerset, NJ

$60K - $75K/yr

Clinical Data Manager FLSA Status: Exempt Location: Onsite (Somerset, New Jersey) Salary: $60,000 - $75,000 Pharmaron is a global CRO (Contract Research Organization) helping pharma and biotech ...

Collabera

Clinical Data Manager

Irvine, CA

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 ...

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Clinical Data Manager information

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How much do clinical data manager jobs pay per hour?

As of Jul 3, 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 degree do you need to be a Clinical Data Manager?

A Clinical Data Manager typically needs at least a bachelor's degree in a health-related field such as life sciences, nursing, or health informatics. Many employers prefer candidates with a master's degree or additional certifications in clinical research or data management. Strong knowledge of database tools and regulatory standards is also important for the role.

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.

What does a clinical data management do?

A clinical data manager is responsible for designing, implementing, and maintaining systems to collect, clean, and analyze data from clinical trials. They ensure data accuracy, integrity, and compliance with regulatory standards using tools like electronic data capture (EDC) systems. This role requires attention to detail, knowledge of Good Clinical Practice (GCP), and often involves collaboration with research teams and data analysts.

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).

How much does a Pfizer Clinical Data Manager make?

A Pfizer Clinical Data Manager typically earns between $80,000 and $120,000 annually, depending on experience, location, and level of responsibility. The role requires strong data management skills and familiarity with clinical trial software such as EDC systems.

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 supporting regulatory submissions and ensuring trial integrity.
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Clinical Data Manager jobs near you
Clinical Data Manager

Clinical Data Manager

EDETEK

Remote

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 10 days ago

Job description

The Clinical Data Manager (CDM) handles project management documentation, clinical data management activities, and system implementations for EDETEK's eClinical, and may be assigned work on other platforms. This includes writing design specifications for the system (forms, reports, etc.) and facilitating testing of system implementations. The CDM is also responsible for all other traditional clinical data management operations and activities such as facilitating database audits, coding, SAE reconciliation, system and module testing, data cleaning, and locking and unlocking of clinical databases. The CDM is responsible for translating the client's Clinical Data Management requirements and expectations into DMP and implementing the clinical data management plans so that the clients' expectations are met. The CDM is responsible for the quality and integrity of the data in the final locked clinical database. The CDM should thoroughly understand the requirements for Good Clinical Data Management services, including its documentation; be willing to be involved in start-up or wrap-up of in-house and client-specific data management projects; have an understanding of the relevant therapeutic indications, study hypotheses, and trial design; and have a solid understanding of database design and structure.
Essential Functions and Responsibilities
  • Support Internal Clinical Data Management Initiatives
  • Complete Traditional and Assigned Data Management Operations/Activities
  • Contribute to Project Success by Conducting Duties per CPM/LSCDM Request
  • Design Case Report Forms (CRFs)
  • Assist in the Development and Maintenance of Systems Used to Support Project Infrastructure
  • Work with Clinical Data Specialists (CDSs) to Execute Data Management Plans
  • Work with Clients/Sponsors as Necessary to Deliver Contracted Clinical Data Management Services and Clinical Data with High Quality and Integrity
  • Code Data per Selected Coding Dictionaries
  • Clean Data
  • Develop / Execute Testing Strategies
  • Assist with Data Transfers, Loading and Integration
  • Complete All Required Documentation per EDETEK and Project Requirements
  • Perform Use Acceptance Testing (UAT) on New Software
  • Classify Clinical Events per Agreed-upon Strategies/Plans Classification.

Requirements
  • Ability to communicate effectively in the English language in person, by phone and in writing.
  • Ability to lead functional meetings
  • Strong attention to detail and accuracy is a must
  • Excellent organizational skills
  • Demonstrated ability to manage multiple projects6. Ability to work collaboratively, effectively, and productively in diverse organization structures.
  • Ability to work independently, take initiative and complete tasks to deadlines: Delivering Excellence, Serving Customers, Accountability and Ownership, Global and Cross-Functional Communication
  • Ability to work in a team-oriented, collaborative environment.
  • Ability to work positively within a continually changing environment.
  • Ability to effectively prioritize and execute tasks in a high-pressure environment.
  • Advanced computer skills and practical knowledge of MS Office and potentially project management software.
Education and Experience Required
  • A Bachelor's degree or equivalent combination of Education/Training/Experience is required. A degree in a scientific, medical, or technological discipline is preferred.
  • A minimum of 2 years of clinical trial or clinical data management experience or similar industry experience/training is required.
  • Prior trial responsibility for the entire data management life-cycle is desirable.
  • Working knowledge of EDC studies and SAS is required.
Work Requirements
  • Corporate office environment or remote.
  • Some travel (5%) may be required with a potential of travel occurring over weekends.
  • Cross-functional interactions

Benefits
Benefits vary by country, but remain competitive. Below is a sample of the benefits offered to U.S. employees.
  • Choice of comprehensive Medical, Vision and Dental Insurance plans
  • Paid vacation time and sick days
  • Corporate holidays annually
  • Participation in the 401K Plan
  • Comprehensive perks and discount programs for AAA, wholesale, insurance, Rx, fitness, pets, entertainment, etc.
  • Health Advocate and Employee Assistance Program
Location
This is a remote position, and we are open to candidates based in the United States and South America.
Equal Opportunity Employer Statement
EDETEK is an equal opportunity employer and does not unlawfully discriminate against employees or applicants for employment on the basis of an individual's race, color, religion, creed, sex, national origin, age, disability, marital status, veteran status or any other status protected by applicable law. This policy applies to all terms, conditions and privileges of employment, including recruitment, hiring, placement, compensation, promotion, discipline, and termination. Whenever possible, the company makes reasonable accommodations for qualified individuals with disabilities to the extent required by law.
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About Edetek

Sourced by ZipRecruiter

Industry

Software development

Company size

201 - 500 Employees

Headquarters location

Princeton, NJ, US

Year founded

2009

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