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Manager, Clinical Data Management

IT ENGAGEMENTS, INC.

Arizona • Today

Easy Apply

Contract

Head of Clinical Data Management

Insmed Incorporated

Remote or New Jersey • Today

Full-time

USD 255,000.00 - 347,500.00 per year

Urgent Need - Data Quality Lead with Clinical Data Exp - 100% Remote

Komplete Teleservices

Remote • Today

Easy Apply

Contract

Depends on Experience

Staff Clinical Informatics Data Architect

Verily Life Sciences

Remote • Today

Full-time

Clinical Program Sourcing & Contracting Manager

SSI People

Remote • 14d ago

Easy Apply

Contract

Depends on Experience

Consultant, Clinical Supplies Management, Biopharma, Global Trials

Eliassen Group

Remote or Almont, Colorado • Today

Contract

Clinical Trial Manager

Eliassen Group

Remote or Almont, Colorado • Today

Full-time

USD 115,000.00 - 120,000.00 per year

Senior RAVE Clinical Database Programmer

Katalyst Healthcares and Lifesciences

Remote or New Jersey • Today

Full-time

Senior Rave Clinical Database Programmer

Katalyst Healthcares and Lifesciences

Remote or New York, New York • Today

Full-time

Clinical Informatics Data Architect

Verily Life Sciences

Remote or Dallas, Texas • Today

Full-time

USD 102,000.00 - 154,000.00 per year

Data Analyst, Clinical Data Effectiveness

Clover Health

Remote • Today

Full-time

USD 77,000.00 - 100,000.00 per year

Clinical Data Analytics

Ab Ovo Inc

Remote • 4d ago

Easy Apply

Contract

Depends on Experience

Data Analyst, Clinical Analytics and Reporting

DaVita Inc.

Remote or Colorado • Today

Full-time

USD 57,784.00 - 85,000.00 per year

Lead Director, Data Science - Clinical AI

CVS Health

Remote or New York, New York • Today

Full-time

USD 144,200.00 - 288,400.00 per year

Clinical Data Analyst (Surgical Tech)

Talent Groups

Remote • 3d ago

Easy Apply

Contract

33 - 38

Senior Clinical Data Analyst – SQL & BigQuery

Datamatics Global Services, Inc.

Remote • 4d ago

Easy Apply

Full-time

Depends on Experience

SIU Clinical Healthcare Fraud Investigator III

Mitchell Martin, Inc.

Remote • 4d ago

Easy Apply

Contract, Third Party

$45 - $55.53

Senior Manager, Master Data Management & Reference Data

Amgen Inc

Remote • Today

Full-time

Manager Data Engineering

Franciscan Health

Remote • Today

Full-time

USD 117,340.82 - 161,343.63 per year

Configuration & Data Manager

SPA

Remote • Today

Full-time

USD 80,000.00 per year

Inpatient Coding/Clinical Data Specialist

Waystar

Remote • Today

Full-time

Clinical Study Administrator

Motion Recruitment Partners, LLC

Remote or Irvine, California • Today

Easy Apply

Contract

Clinical Project Coordinator

Motion Recruitment Partners, LLC

Remote or Irvine, California • Today

Easy Apply

Contract

Clinical Research Scientist III - (Director/Assoc. Director level)

NexInfo Solutions, Inc.

Remote or Hybrid in Parsippany-Troy Hills, New Jersey • 18d ago

Easy Apply

Third Party, Contract

$100 - $110

Clinical Contracts Associate

Arnex Solutions LLC

Remote • Today

Full-time, Third Party

Depends on Experience

Clinical Systems Administrator

Dycom Industries

Flagstaff, Arizona • Today

Full-time

Remote Job - Clinical Scientist Consultant SME Level - Neurology *Pivotal Studies

Cube Hub, Inc.

Remote or Foster City, California • Today

Easy Apply

Contract

$DOE

Clinical Project Manager with RBQM, Veeva, CTMS, eTMF, EDC

Arrowminds inc

Remote • 19d ago

Easy Apply

Full-time

Depends on Experience

Clinical Study Assistant

Motion Recruitment Partners, LLC

Remote or New Brunswick, New Jersey • Today

Easy Apply

Contract

Medical Monitoring Implementation Lead / Clinical SME

Saama Technologies, LLC

Remote • Today

Easy Apply

Full-time, Third Party

Depends on Experience

Job Details

Skills

Project Manager
Data Management
SAS
Clinical
FDA
CRF
Study startup
Pharmacuetical
Biotech

Summary

Manager, Clinical Data Management

IT Engagements is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. We have an immediate opening for the below position with one of our premium clients.

Role: Manager, Clinical Data Management (Contract Role)

Location: Remote

DUTIES:

The Manager, Clinical Data Management leads the data management components of a clinical trial ranging from small early phase to large global and late phase programs.
The Manager, Clinical Data Management is responsible for ensuring study launch, conduct, and closeout are performed according to Client's quality standards, Standard Operating Procedures (SOPs), Good Clinical Practices (Google Cloud Platforms), and International Conference on Harmonization (ICH) guidelines to fulfill all federal and local regulations.
The assigned clinical trial(s) may be high complexity or high risk. Duties include serving as the primary data management liaison with vendors and senior management.
This position will manage essential duties and responsibilities as independently as possible, with guidance and oversight provided by senior data management when needed.

Skills:

Maintain effective communication with vendors and Client internal project team through oral and written correspondence, project status and progress reports. Manage the planning, implementation and overall direction of executing clinical trial data management activities including protocol review, electronic system configuration, Case Report Form (CRF/eCRF) design, database development, validation programming, and discrepancy management. Prepare information for internal meetings.
Maintain and evaluate project progress by managing timelines and other tracking/analysis tools. Design, produce and distribute standard and customized status, resourcing, and tracking reports as well as functional area plans, to appropriate team members and senior management. Work on problems of a diverse scope. Exercise judgment in managing tasks within generally defined practices and policies in selecting methods and techniques to track and manage timelines, risk, and data quality.
Manages the cross-functional collaboration, development, and maintenance of the components of the study Data Management Plan (DMP) and data management deliverables including the Case Report Form (CRF), CRF completion guidelines, SAS annotated CRFs, data handling plan, data review plan, edit check specifications, data transfer specifications, data quality plan, etc. Manage the interaction with data management vendors to ensure that data management tasks remain on target according to project timelines. Proactively organize on-going data review throughout the conduct of the study to ensure timely and appropriate identification of errors and discrepancies. Facilitate the correction of errors and discrepancies through the site query process, document permanent data issues, communicate issues with team members, and deliver a quality locked database for analysis. Provide input to the data management study budget and responsible for managing assigned vendor budget(s). Lead new data management initiatives such as establishing capacity for electronic data capture and clinical outcome assessments. Conduct CRO data management function inspections and audits. Contribute to the development and implementation of departmental policies, standards and process improvement initiatives.

EDUCATION:

A bachelor's degree in clinical, biological or mathematical sciences, nursing degree, or equivalent related field education and experience is required.
A master's degree is preferred. A minimum of 8 years actively managing clinical research projects in collaboration with other functional areas with at least 2 years successfully managing CROs is CROs is preferred.
Previous supervisory, and/or dermatology experience is preferred. A thorough knowledge of FDA regulations, drug development and clinical monitoring procedures is required.
Demonstrated problem solving abilities and strong presentation, documentation, organizational, and interpersonal skills as well as a team-oriented approach are required.
Excellent written and verbal communication skills are required. Demonstrated proficiency with ICH, GCDMP, and Google Cloud Platform is required.
Fluent English is required. Proficient computer skills using Word, Excel, PowerPoint, MS Project, email and the internet are required.
Demonstrated self-starter with the ability to mentor and handle multiple tasks to meet deadlines while delivering high quality work in a dynamic work environment.
Must possess excellent project management skills and have demonstrated ability to develop data management processes and training.

Thank You

Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.

Dice Id: 91119149
Position Id: 2026-2444
Posted 5 hours ago

Fitment

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Similar Jobs

Head of Clinical Data Management

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At Insmed, every moment and every patient counts - and so does every person who joins in. As a global biopharmaceutical company dedicated to transforming the lives of patients with serious and rare diseases, you'll be part of a community that prioritizes the human experience, celebrates curiosity, and values every person's contributions to meaningful progress. That commitment has earned us recognition as Science magazine's No. 1 Top Employer for five consecutive years, certification as a Great P

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Job Description This role provides strategic and operational leadership for Clinical Data Management activities supporting the company's clinical development portfolio. This position is responsible for ensuring the delivery of high-quality, reliable, and inspection-ready clinical data through effective planning, oversight, and execution of data management activities across both internally managed and outsourced clinical studies. The Director partners closely with cross-functional stakeholders,

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Associate Clinical Data Manager (CDM)

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Associate Clinical Data Management Maplegrove - MN Role Summary The Associate Clinical Data Manager supports the planning and execution of clinical study data management activities. Under the direction of a manager, this role leads cross-functional teams through case report form development, database setup, data review, and data cleaning processes to ensure the integrity and quality of clinical study data throughout the lifecycle of an investigation. Key Responsibilities Leads cross-functi

Full-time, Third Party

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Campus - Clinical Data Management Intern

Indianapolis, Indiana

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At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life-changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work-but i

Full-time

USD 76,000.00 - 85,000.00 per year

Job Details

Skills

Project Manager
Data Management
SAS
Clinical
FDA
CRF
Study startup
Pharmacuetical
Biotech

Summary

Manager, Clinical Data Management

Role: Manager, Clinical Data Management (Contract Role)

Location: Remote

DUTIES:

The Manager, Clinical Data Management leads the data management components of a clinical trial ranging from small early phase to large global and late phase programs.
The Manager, Clinical Data Management is responsible for ensuring study launch, conduct, and closeout are performed according to Client's quality standards, Standard Operating Procedures (SOPs), Good Clinical Practices (Google Cloud Platforms), and International Conference on Harmonization (ICH) guidelines to fulfill all federal and local regulations.
The assigned clinical trial(s) may be high complexity or high risk. Duties include serving as the primary data management liaison with vendors and senior management.
This position will manage essential duties and responsibilities as independently as possible, with guidance and oversight provided by senior data management when needed.

Skills:

Maintain effective communication with vendors and Client internal project team through oral and written correspondence, project status and progress reports. Manage the planning, implementation and overall direction of executing clinical trial data management activities including protocol review, electronic system configuration, Case Report Form (CRF/eCRF) design, database development, validation programming, and discrepancy management. Prepare information for internal meetings.
Maintain and evaluate project progress by managing timelines and other tracking/analysis tools. Design, produce and distribute standard and customized status, resourcing, and tracking reports as well as functional area plans, to appropriate team members and senior management. Work on problems of a diverse scope. Exercise judgment in managing tasks within generally defined practices and policies in selecting methods and techniques to track and manage timelines, risk, and data quality.
Manages the cross-functional collaboration, development, and maintenance of the components of the study Data Management Plan (DMP) and data management deliverables including the Case Report Form (CRF), CRF completion guidelines, SAS annotated CRFs, data handling plan, data review plan, edit check specifications, data transfer specifications, data quality plan, etc. Manage the interaction with data management vendors to ensure that data management tasks remain on target according to project timelines. Proactively organize on-going data review throughout the conduct of the study to ensure timely and appropriate identification of errors and discrepancies. Facilitate the correction of errors and discrepancies through the site query process, document permanent data issues, communicate issues with team members, and deliver a quality locked database for analysis. Provide input to the data management study budget and responsible for managing assigned vendor budget(s). Lead new data management initiatives such as establishing capacity for electronic data capture and clinical outcome assessments. Conduct CRO data management function inspections and audits. Contribute to the development and implementation of departmental policies, standards and process improvement initiatives.

EDUCATION:

A bachelor's degree in clinical, biological or mathematical sciences, nursing degree, or equivalent related field education and experience is required.
A master's degree is preferred. A minimum of 8 years actively managing clinical research projects in collaboration with other functional areas with at least 2 years successfully managing CROs is CROs is preferred.
Previous supervisory, and/or dermatology experience is preferred. A thorough knowledge of FDA regulations, drug development and clinical monitoring procedures is required.
Demonstrated problem solving abilities and strong presentation, documentation, organizational, and interpersonal skills as well as a team-oriented approach are required.
Excellent written and verbal communication skills are required. Demonstrated proficiency with ICH, GCDMP, and Google Cloud Platform is required.
Fluent English is required. Proficient computer skills using Word, Excel, PowerPoint, MS Project, email and the internet are required.
Demonstrated self-starter with the ability to mentor and handle multiple tasks to meet deadlines while delivering high quality work in a dynamic work environment.
Must possess excellent project management skills and have demonstrated ability to develop data management processes and training.

Thank You

Dice Id: 91119149
Position Id: 2026-2444
Posted 5 hours ago

Fitment

Dice Job Match Score™

🔢 Crunching numbers...

Create job alert

Never miss an opportunity! Create an alert based on the job you applied for.

Similar Jobs

Head of Clinical Data Management

Remote or New Jersey

•

Today

Full-time

USD 255,000.00 - 347,500.00 per year

Director, Data Management

Waltham, Massachusetts

•

Today

Full-time

USD 205,000.00 - 230,000.00 per year

Associate Clinical Data Manager (CDM)

Maple Grove, Minnesota

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Campus - Clinical Data Management Intern

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