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Temporary Contract Clinical Data Manager Jobs in Colorado

Clinical Data Engineer

Denver, CO · 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 ...

JOB SUMMARY: The Data Manager is responsible for maintaining the integrity, consistency, and ... Experience managing CM/DM on DoD, NASA, or government contract programs. * Proficiency with CM/DM ...

JOB SUMMARY: The Data Manager is responsible for maintaining the integrity, consistency, and ... Experience managing CM/DM on DoD, NASA, or government contract programs. * Proficiency with CM/DM ...

Senior Data Manager

Denver, CO

$69.25 - $92.75/hr

DAMA Data Management certification (equivalent credential) * ITIL 4 Foundation * Certified ... Employees are required to comply with any vaccination requirements mandated by contract, applicable ...

Clinical data exchange and coding standards, including HL7, FHIR, and ICD * Data operations (ie ... Manage day-to-day stakeholder relationships and align technical delivery to business and program ...

This role plays a critical role in identifying cost savings, reducing unwarranted clinical ... Responsibilities include benchmarking, gap analysis, pricing and contract review, utilization ...

Clinical EHR Data Analyst

Durango, CO · On-site

$24.87 - $49.85/hr

Conduct data analysis for clinical improvements, regulatory compliance, and system enhancements ... and manage system updates. * Implement and oversee system testing, user training, and ...

Clinical EHR Data Analyst

Durango, CO · On-site

$24.87 - $49.85/hr

Conduct data analysis for clinical improvements, regulatory compliance, and system enhancements ... and manage system updates. * Implement and oversee system testing, user training, and ...

Enter clinical trial data into case report forms (CRFs) or clinical data management systems (CDMS), ensuring alignment with source documents. * Perform data entry in compliance with Good Clinical ...

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Temporary Contract Clinical Data Manager information

What is a temporary contract clinical data manager?

Temporary Contract Clinical Data Managers are professionals hired on a short-term basis to oversee the collection, management, and quality assurance of clinical trial data. They ensure that the data from clinical studies is accurate, complete, and compliant with regulatory standards. These roles are often project-based and may involve tasks such as designing data collection systems, monitoring data integrity, and preparing reports for regulatory submissions. Temporary contracts allow organizations to meet fluctuating project needs without committing to permanent hires.

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

To thrive as a Temporary Contract Clinical Data Manager, you need expertise in clinical data management, data integrity, and regulatory compliance, usually supported by a degree in life sciences or a related field. Proficiency with data management systems such as Medidata Rave, Oracle Clinical, and knowledge of CDISC standards, along with relevant certifications like Society for Clinical Data Management (SCDM), is commonly required. Strong attention to detail, problem-solving, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring high-quality data. These skills and qualifications are essential to ensure accurate, timely, and compliant management of clinical trial data, directly impacting the success of clinical research projects.

What are some common challenges faced by temporary contract clinical data managers, and how can they prepare to address them?

Temporary Contract Clinical Data Managers often face the challenge of quickly adapting to new systems, processes, and team dynamics within a short timeframe. They are expected to efficiently manage clinical trial data, ensure data quality, and adhere to strict regulatory standards despite limited onboarding. To succeed, it's helpful to familiarize oneself with common clinical data management platforms, maintain strong organizational skills, and be proactive in communicating with study teams. Building rapport with key colleagues early on can also help navigate project-specific requirements and ensure smooth collaboration.

What is the difference between Temporary Contract Clinical Data Manager vs Clinical Data Coordinator?

AspectTemporary Contract Clinical Data ManagerClinical Data Coordinator
CredentialsBachelor's degree in life sciences, experience with clinical data systemsBachelor's degree, familiarity with data entry and management
Work EnvironmentContract-based, often in pharmaceutical or biotech companiesFull-time, in clinical research teams or CROs
Employer & IndustryPharmaceutical, biotech, CROsResearch sites, CROs, pharmaceutical companies
Search & Comparison IntentUnderstanding contract roles, data management tasksData entry, coordination, and support roles

The Temporary Contract Clinical Data Manager typically oversees data management during clinical trials on a contract basis, focusing on data quality and compliance. In contrast, a Clinical Data Coordinator handles data entry and coordination tasks within ongoing studies. Both roles require similar credentials but differ mainly in scope, duration, and responsibilities.

What are popular job titles related to Temporary Contract Clinical Data Manager jobs in Colorado?

For Temporary Contract Clinical Data Manager jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Temporary Contract Clinical Data Manager jobs in Colorado look for?

The top searched job categories for Temporary Contract Clinical Data Manager jobs in Colorado are:

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

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

Infographic showing various Temporary Contract Clinical Data Manager job openings in Colorado as of August 2026, with employment types broken down into 86% Full Time, 12% Part Time, and 2% Contract. Highlights an 82% Physical, 2% Hybrid, and 16% Remote job distribution.

Senior Clinical Data Manager (Remote - US)

MMS

Denver, CO • On-site

Full-time

Posted 19 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