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Manager Clinical Data Management Jobs in Colorado

Clinical Data Engineer

Denver, CO ยท On-site

$85K - $100K/yr

What You'll Do The Data Operations department provides data management, integration, and reporting services for multiple external and internal consumers. The Clinical Data Engineer will be ...

Manage configuration, patching, upgrades, and troubleshooting for Axway Secure Transport (ST), ensuring secure, reliable file transfer for clinical data exchange with CROs, labs, and regulatory ...

Data Management Specialist

Denver, CO ยท On-site

$70K - $92K/yr

Data Management Specialist Location: Onsite, Denver, CO Position Summary The Data Management Specialist supports the Client's National Customer Service Improvement Project (CSIP) by ensuring the ...

Project & Operations Management: Lead the end-to-end development and day-to-day operations of ... Synthesize complex clinical data and analytical findings, presenting insights and actionable ...

Data Management Engineer

Pueblo, CO ยท On-site

$112K - $135K/yr

This person is responsible for developing and automating analytical tools and data process workflows that support order management and bill of material.This person will execute product changes within ...

New

Data Management Engineer

Pueblo, CO

$112K - $135K/yr

This person is responsible for developing and automating analytical tools and data process workflows that support order management and bill of material.This person will execute product changes within ...

New

Data Management Engineer

Pueblo, CO ยท On-site

$112K - $135K/yr

This person is responsible for developing and automating analytical tools and data process workflows that support order management and bill of material. * This person will execute product changes ...

New

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Manager Clinical Data Management information

See Colorado salary details

$20

$60

$86

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

As of Sep 12, 2026, the average hourly pay for manager clinical data management in Colorado is $60.11, according to ZipRecruiter salary data. Most workers in this role earn between $47.50 and $71.54 per hour, depending on experience, location, and employer.

What are the roles and responsibilities of a manager clinical data management?

A Manager of Clinical Data Management oversees the collection, processing, and quality assurance of clinical trial data to ensure accuracy and regulatory compliance. They lead teams of data managers, develop data management plans, and coordinate with clinical and regulatory teams to resolve data discrepancies. Their responsibilities often include implementing data standards, ensuring data integrity, and supporting audits and submissions to regulatory authorities. This role requires strong leadership skills, attention to detail, and expertise in clinical trial processes and data management systems.

What are the key skills and qualifications needed to thrive as a manager clinical data management?

To thrive as a Manager Clinical Data Management, you typically need a strong background in life sciences, clinical research, and data management, often supported by a relevant degree and experience in clinical trials. Expertise with clinical data management systems (such as Medidata Rave or Oracle Clinical), knowledge of CDISC standards, and certifications like CCDM are highly valued. Strong leadership, attention to detail, and effective communication are crucial soft skills for coordinating teams and ensuring data integrity. These skills are essential to ensure high-quality, compliant clinical data that supports successful regulatory submissions and advances clinical research.

What are some typical challenges faced by a manager clinical data management, and how can they be addressed?

Managers in Clinical Data Management often face challenges such as ensuring data quality across multiple clinical sites, meeting tight regulatory deadlines, and coordinating cross-functional teams including data analysts, clinical operations, and biostatisticians. To address these challenges, strong project management skills, proactive communication, and the implementation of robust data validation procedures are essential. Additionally, staying up-to-date with evolving regulatory requirements and investing in team training can help maintain data integrity and streamline workflows.

What is the difference between Manager Clinical Data Management vs Clinical Data Coordinator?

AspectManager Clinical Data ManagementClinical Data Coordinator
ResponsibilitiesOversees data management processes, manages teams, ensures data quality and complianceCollects, enters, and verifies clinical trial data, supports data cleaning
Required SkillsProject management, leadership, data management expertiseAttention to detail, data entry, basic understanding of clinical data
CertificationsCDMP, SAS, or related certifications often preferredTypically no advanced certifications required
Work EnvironmentClinical research organizations, pharmaceutical companies, CROsSimilar settings, often working under supervision of managers

While both roles involve clinical data, the Manager Clinical Data Management leads data strategies and teams, whereas the Clinical Data Coordinator focuses on data entry and verification tasks. The manager role requires more leadership and strategic skills, while the coordinator role is more operational and detail-oriented.

What are the most commonly searched types of Clinical Data Management jobs in Colorado?

The most popular types of Clinical Data Management jobs in Colorado are:

What cities in Colorado are hiring for Manager Clinical Data Management jobs?

Cities in Colorado with the most Manager Clinical Data Management job openings:

Infographic showing various Manager Clinical Data Management job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 13% Part Time, 1% Temporary, and 2% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $125,035 per year, or $60.1 per hour.

Senior Clinical Data Manager (Remote - US)

Denver, CO โ€ข On-site

MMS
Pharmaceutical and Medicine Manufacturingย โ€ขย 1 - 10 employees

Full-time

Posted 25 days ago


Job description

Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team? MMS is a award-winning, data-focused clinical research organization (CRO). We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges. With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive. Join us at MMS and be part of a team that is shaping the future of clinical research.
 
Discover more about our exciting opportunities and why MMS is a great place to advance your career. Visit www.mmsholdings.com or follow MMS on LinkedIn.
Roles and Responsibilities:
  • Confidently displays excellent internal and external customer service.
  • Has proficiency and knowledge of multiple EDC systems; applies this knowledge to advise customers regarding the best-fit EDC solution.
  • Interacts directly and independently with DM suppliers including EDC and/ or IWR; expert communicator, where necessary negotiating with supplier to meet business needs.
  • Interacts directly and independently with client to coordinate all facets of projects; expert communicator; builds and maintains strong client contacts and relationships.
  • Responsible for entire data management process from study set-up to study close-out; primary contact on all data management study-specific issues; has high-level knowledge of drug development as it pertains to data management.
  • Actively participates in protocol review with clients, providing suggestions regarding ability to capture protocol information in database successfully.
  • Strong understanding of GCP/ ICH guidelines and FDA regulations, as applicable to data management.
  • Creates training exercises; serves as mentor and trains new clinical data managers.
  • Provides oversight and resolves all issues in data management study processing activities including CRF tracking and data entry, integration of external electronic data (e.g., lab data) with clinical database, data validation and review, query processing and resolution, adverse event and medication coding, SAE reconciliation, database lock and database QC audits.
  • Oversees and develops data management study documentation including Case Report Forms, CRF Completion Guidelines, Database Design via annotated CRFs, Validation specifications (edit checks), and Data Management Plan.
  • Preparation of any study tracking and metric reports for use by the study team.
  • Oversees execution of user acceptance testing (UAT) of study-specific systems and applications.
  • Interacts with cross-functional team members to ensure completion of all timelines and studies.
  • Participates in data management and/or organizational initiatives.
  • Initiates SOP updates and provide specifications for DM systems/ tools and process enhancements.
  • May act as resource for QC activities in collaboration with QC Coordinator.
  • Understands and follows processes related to project management as appropriate for data management projects (e.g., updating PSS, close-out procedures, etc.).
  • Confident, positive attitude displayed towards clients and projects.
  • Willingness to learn new skills and expand knowledge of drug development.
  • Leads data management projects with little management oversight.
  • Ability to work independently and resolve issues.
  • Ability to clearly articulate the DM services offered at company, including pros and cons of various DM approaches (specific to a client or operating model). To include potential attendance at (web or remote) capabilities and bid defense meetings.
Requirements:
  • Bachelor’s or Master’s Degree in scientific or health care field preferred with industry or relevant experience.
  • 5+ years’ experience in data management field with a minimum of 1 year of experience leading projects.
  • Extensive knowledge of paper CRF study systems, EDC, and hybrid CDM systems.
  • Extensive knowledge of Clinical Operations SOPs and Working Practices.
  • Excellent verbal and written communication skills, as well as, interpersonal and organizational skills.

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M. M. S. logo

About M. M. S.

Sourced by ZipRecruiter

Industry

Pharmaceutical and medicine manufacturing

Company size

1 - 10 Employees

Headquarters location

Los Angeles, CA, US

Year founded

1980