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Associate Director Clinical Data Management Jobs in Colorado

Carina Health Network

Clinical Data Engineer

Denver, CO · On-site

$85K - $100K/yr

Clinical Data Engineer - Remote, Must Live in State of Colorado Join Carina Health Network and help ... Is flexible, organized, self-directed, able to prioritize multiple tasks, and able to manage a full ...

Flourish Research

Data Entry Clerk

Denver, CO

$21 - $26/hr

Enter clinical trial data into case report forms (CRFs) or clinical data management systems (CDMS ... High school diploma or equivalent required; associate's degree preferred * Degree in Health ...

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Associate Director Clinical Data Management information

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How much do associate director clinical data management jobs pay per hour?

As of Aug 25, 2026, the average hourly pay for associate director clinical data management in Colorado is $40.96, according to ZipRecruiter salary data. Most workers in this role earn between $30.82 and $40.96 per hour, depending on experience, location, and employer.

What is an associate director clinical data management?

An Associate Director of Clinical Data Management is a senior professional responsible for overseeing the planning, execution, and management of data collected in clinical trials within the pharmaceutical or biotechnology industry. They ensure that all clinical data is accurate, secure, and compliant with regulatory standards. This role typically involves leading teams, developing data management strategies, collaborating with cross-functional departments, and ensuring that projects are delivered on time and within budget. Associate Directors also play a key role in establishing best practices and continuous process improvements within the data management function.

What are the key skills and qualifications needed to thrive as an associate director clinical data management, and why are they important?

To thrive as an Associate Director Clinical Data Management, you need a strong background in clinical research, data management, and regulatory compliance, typically supported by a life sciences degree and several years of experience in clinical data management. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) platforms, and industry standards such as CDISC or GCP is crucial, with certifications like CCDM being advantageous. Leadership, strategic thinking, and excellent communication skills help drive cross-functional teams and ensure accurate data delivery. These competencies are vital because they ensure high-quality, compliant data management that supports successful clinical trials and regulatory submissions.

What are some common challenges faced by an associate director clinical data management, and how can they be addressed?

Associate Directors in Clinical Data Management often encounter challenges such as maintaining data quality across multiple studies, managing tight timelines, and ensuring compliance with evolving regulatory requirements. To address these, they implement robust data review processes, foster close collaboration between cross-functional teams (like biostatistics, clinical operations, and IT), and promote continuous training for their teams. Strong leadership and effective communication are key to navigating these challenges while delivering high-quality data for clinical trials.

What is the difference between Associate Director Clinical Data Management vs Clinical Data Manager?

AspectAssociate Director Clinical Data ManagementClinical Data Manager
ResponsibilitiesOversees data management teams, develops strategies, ensures data quality and complianceManages data collection, validation, and database setup for clinical trials
Required CredentialsBachelor's/Master's in life sciences, experience in data management, leadership skillsBachelor's in life sciences, experience in clinical data handling, technical skills
Work EnvironmentSenior-level, strategic, often in larger organizations or departmentsOperational, hands-on, often in CROs or pharmaceutical companies

The Associate Director Clinical Data Management typically holds a higher strategic role, overseeing teams and ensuring data quality across projects, while the Clinical Data Manager focuses on day-to-day data handling tasks. Both roles require similar educational backgrounds and technical skills, but differ in scope and level of responsibility.

What are popular job titles related to Associate Director Clinical Data Management jobs in Colorado?

For Associate Director Clinical Data Management jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Associate Director Clinical Data Management jobs in Colorado look for?

The top searched job categories for Associate Director Clinical Data Management jobs in Colorado are:

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

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

Associate Director Clinical Data Management jobs near you
Infographic showing various Associate Director Clinical Data Management job openings in Colorado as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 84% Physical, 2% Hybrid, and 14% Remote job distribution, with an average salary of $85,194 per year, or $41 per hour.

Senior Data Manager, CRO Oversight, Early Phase Studies

Eliassen Group

Almont, CO • On-site

$80 - $90/hr

Other

Medical, Dental, Vision, Life, Retirement

Posted 24 days ago

Job description

Description:
Remote
Our client is seeking a Senior Data Manager to provide operational support across multiple early-stage clinical studies in a wide variety of therapeutic areas. This individual will partner with cross-functional study teams and external CROs to ensure the timely delivery of high-quality clinical data that supports informed decision-making throughout Phase 1 first-in-human and Phase 1b/2 patient studies. This is a highly operational role requiring the ability to manage multiple programs simultaneously and serve as a trusted partner to study teams, while maintaining flexibility in a fast-paced, resource-efficient environment. This individual will report into our client's Associate Director of Data Management & Technology.
Due to client requirements, applicants must be willing and able to work on a w2 basis. For our w2 consultants, we offer a great benefits package that includes Medical, Dental, and Vision benefits, 401k with company matching, and life insurance.
Rate: $80.00 to $90.00/hr. w2
Responsibilities:
  • Review and contribute to study-specific data management plans, edit check specifications, data review plans, CRF/eCRF design, database specifications, and data transfer agreements.
  • Participate in protocol review to ensure data collection strategies support study objectives while minimizing operational complexity.
  • Serve as sponsor-side oversight of CRO and specialty vendor data management deliverables, including scope and specifications, timelines, quality, metrics review, and issue escalation, while retaining accountability for partner-executed work.
  • Own database build oversight, user acceptance testing (UAT), database lock activities, and study closeout.
  • Drive ongoing data review, query management, reconciliation activities including safety, laboratory, and external vendor data, and issue resolution throughout study conduct.
  • Deliver clean, near-real-time data on compressed timelines to support dose-escalation decisions, safety review committee meetings, DLT assessment, and interim data cutoffs.
  • Monitor data quality metrics and proactively identify risks that may impact study timelines, database quality, or regulatory readiness.
  • Support the preparation for interim analyses, regulatory submissions, and clinical study reports by ensuring timely, high-quality datasets.
  • Serve as the Medidata user administrator at the URL level, including assigning access to CRO study builders, coders, and data managers at the CRO.
  • Evaluate and recommend improvements to clinical data management systems, technologies, and workflows as appropriate.
  • Contribute to inspection readiness activities and ensure compliance with applicable Google Cloud Platform, ICH, FDA, EMA, and other regulatory requirements.

Experience Requirements:
  • Bachelor's degree in Life Sciences, Computer Science, Biostatistics, Data Science, or related field.
  • 8-12 years of data management experience, with the majority on the sponsor side.
  • Minimum 3+ years leading Phase 1 studies, including first-in-human healthy volunteer SAD/MAD and Phase 1b/2 patient studies as Lead Data Manager.
  • Sponsor-side oversight of CRO and specialty vendor data management, including specification review, deliverable and timeline oversight, and escalation of underperformance.
  • Hands-on Medidata Rave experience, including study configuration, edit check specification, and Rave reporting. Working knowledge of other EDC platforms such as Veeva or Oracle InForm is a plus.
  • Familiarity with CDISC standards (SDTM), data reconciliation processes, coding dictionaries, and database lock activities.
  • Solid understanding of ICH-Google Cloud Platform, FDA, EMA, and other applicable clinical data management regulations and guidance.
  • Excellent analytical, organizational, and communication skills with strong attention to detail and the ability to collaborate across cross-functional scientific and operational teams.
  • Nice to have: Experience working alongside a Biometrics vendor responsible for biostatistical activities.

Education Requirements:
Bachelor's degree in Life Sciences, Computer Science, Biostatistics, Data Science, or related field.
Recruitment Transparency Notice

Eliassen Group values transparency in our recruitment practices. Please be advised that Eliassen Group utilizes artificial intelligence (AI) tools as part of its initial application screening and hiring process. You may receive email and SMS notifications from the Eliassen Virtual Recruiting Team (, ) inviting you to complete a brief voice screening as part of your application process. These tools assist our hiring teams in different ways, including but not limited to, assistance in reviewing application materials to help identify candidates whose qualifications most closely match the requirements of the position. All AI-assisted evaluations and responses are reviewed by human recruiters before any hiring decisions are made. The use of AI in our process is intended to support fairness, efficiency, and consistency, and Eliassen Group takes measures to prevent bias or discrimination in connection with its hiring practices. By proceeding, you acknowledge, agree, and consent to Eliassen Group's use of these tools, including AI tools, as part of the application and hiring process.
Skills, experience, and other compensable factors will be considered when determining pay rate. The pay range provided in this posting reflects a W2 hourly rate; other employment options may be available that may result in pay outside of the provided range.
W2 employees of Eliassen Group who are regularly scheduled to work 30 or more hours per week are eligible for the following benefits: medical (choice of 3 plans), dental, vision, pre-tax accounts, other voluntary benefits including life and disability insurance, 401(k) with match, and sick time if required by law in the worked-in state/locality.
If anyone reaches out to you about an open position connected with Eliassen Group, please ensure that you are working directly with us by confirming the following:
When you work with Eliassen Group, all email communication will come from an Eliassen.com address, never Gmail, Yahoo, etc.
Eliassen Group will never ask you for personal information (home address, bank account, or check routing number) until you have worked with someone clearly associated with Eliassen Group.
If you have any indication of fraudulent activity, please contact .
About Eliassen Group:
Eliassen Group is a strategic consulting firm that helps organizations reach further and achieve more through our technology, business advisory, and life sciences solutions. For nearly 40 years, we have combined exceptional people, deep domain expertise, and intelligent capabilities to expand our clients' capacity and accelerate meaningful outcomes. We are driven by a purpose to positively impact the lives of our employees, clients, consultants, and the communities we serve.
Eliassen is committed to building a diverse and inclusive team from a variety of backgrounds, perspectives, and skills. We are an Equal Opportunity and Affirmative Action Employer and all employment decisions are based on merit, performance, and business needs. Eliassen does not discriminate on the basis of race, color, gender identity or expression, sexual preference or orientation, sex (including pregnancy, childbirth, and related medical conditions), marital status, creed, religion, physical or mental disability, genetic information, military or veteran status, age, ancestry, national origin, citizenship status, prohibited criminal record inquiries of applicants and employees, or any other category protected by federal, state, or local laws.
Don't miss out on our referral program! If we hire a candidate that you refer us to then you can be eligible for a $1,000 referral check!
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About Eliassen Group

Sourced by ZipRecruiter

Eliassen Group provides strategic consulting and talent solutions to drive our clients' innovation and business results. Our purpose is to positively impact the lives of our employees, clients, consultants, and the communities in which we operate. Leveraging over 30 years of success, our expertise in talent solutions, life sciences consulting, Agile consulting, cloud services, risk management, business optimization, and managed services enables us to partner with our clients to execute their business strategy and scale effectively. Headquartered in Reading, MA, and with offices from coast to coast, Eliassen Group offers local community presence and deep networks, as well as national reach.

Industry

It services

Company size

5,001 - 10,000 Employees

Headquarters location

Reading, MA, US

Year founded

1989

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