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Associate Director Clinical Data Management Jobs

MCRA

Associate Data Manager

Washington, DC · On-site

Knowledge of clinical data management processes and GCPs preferred. * Computer literacy and ... Must be self-motivated and perform excellent work with limited direct oversight/guidance. * Ability ...

DTCC

Data Management Associate Director

Tampa, FL · On-site

As a core member of the Data Management Team within Enterprise Data Solutions, an Associate Director will be responsible for driving projects forward, managing key deliverables, and helping to drive ...

IQVIA

Lead Clinical Data Manager (Remote)

New York, NY · Remote

$68K - $217K/yr

No less than 7 years of direct clinical data management experience * 5+ years in a Lead Clinical Data Management role REQUIRED. * Your previous roles/job titles may include Clinical Data Manager ...

IQVIA

Lead Clinical Data Manager (Remote)

Tampa, FL · Remote

$68K - $217K/yr

No less than 7 years of direct clinical data management experience * 5+ years in a Lead Clinical Data Management role REQUIRED. * Your previous roles/job titles may include Clinical Data Manager ...

IQVIA

Lead Clinical Data Manager (Remote)

Charleston, WV · Remote

$68K - $217K/yr

No less than 7 years of direct clinical data management experience * 5+ years in a Lead Clinical Data Management role REQUIRED. * Your previous roles/job titles may include Clinical Data Manager ...

IQVIA

Lead Clinical Data Manager (Remote)

Anaheim, CA · Remote

$68K - $217K/yr

No less than 7 years of direct clinical data management experience * 5+ years in a Lead Clinical Data Management role REQUIRED. * Your previous roles/job titles may include Clinical Data Manager ...

IQVIA

Lead Clinical Data Manager (Remote)

Durham, NC · Remote

$68K - $217K/yr

No less than 7 years of direct clinical data management experience * 5+ years in a Lead Clinical Data Management role REQUIRED. * Your previous roles/job titles may include Clinical Data Manager ...

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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 Jun 9, 2026, the average hourly pay for associate director clinical data management in the United States is $38.95, according to ZipRecruiter salary data. Most workers in this role earn between $29.33 and $38.94 per hour, depending on experience, location, and employer.

What are 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 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 some common challenges faced by an Associate Director of 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.
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Associate Director Clinical Data Management jobs near you
Infographic showing various Associate Director Clinical Data Management job openings in the United States as of June 2026, with employment types broken down into 2% As Needed, 74% Full Time, 22% Part Time, 1% Temporary, and 1% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.

Senior Manager, Clinical Data Management

Latigo Biotherapeutics

San Francisco, CA • On-site

$180K - $195K/yr

Full-time

Posted 6 days ago

Job description

POSITION DESCRIPTION
Latigo is seeking a Senior Manager of Clinical Data Management to lead and oversee data management activities for assigned clinical studies, which includes, but is not limited to: CRF design and development, CRF standardization, ongoing data review and cleaning, rolling/interim/final database locks, and clinical data archival. They will work collaboratively with other internal and external clinical study team members across Clinical Operations, Biostatistics, Clinical Development and Translational Science. They shall be adept at utilizing and managing EDC systems, managing clinical data workflows and processes, and ensuring clinical trial data integrity and quality in their assigned studies to ensure high quality data in support of analysis for regulatory submissions, safety reporting and publications.
Essential duties and responsibilities:
  • Manage and oversee CROs/vendors in clinical data management on clinical trials within assigned program.
  • Oversee the data management activities and deliverables from EDC build to final database lock and their timelines for assigned studies to ensure quality, efficiency and consistency.
  • Perform detailed reviews of data management specific plans and database specifications to ensure a built-in quality approach.
  • Perform User Acceptance Testing (UAT) on EDC, IRT and eCOA systems.
  • Develop study metrics reports and other reports as needed.
  • Work with vendors to set up and review data transfer specifications.
  • Oversee vendor data reconciliation (i.e. central laboratory data, SAE) to include quality control and timely review of queries.
  • Lead the creation of data review plans for internal cross-functional clinical data review activities.
  • Oversee EDC user administration and access for assigned studies.
  • Collaborate and communicate regularly with internal and external team members across other clinical trials and programs for consistency and standardization across programs to promote increasing efficiency.
  • Proactively identify potential issues affecting timeline, milestones, or deliverables, and propose strategies to mitigate or resolve.
  • Direct the development of CRFs and database design with cross-functional input and adherence to CDASH/CDISC standards and standards developed internally at Latigo Bio.
  • Participate in the creation of SOPs that are necessary for internal Clinical Data Management activities.
  • QC filing of data management documentation in the electronic Trial Master File (eTMF).
  • Maintain internal data management study level documentation in audit ready status, as applicable.
  • Perform other duties as requested.

Preferred Education & Experience:
  • Bachelor's degree required, at a minimum.
  • 7+ years of relevant industry experience in clinical data management.
  • Self-motivated and highly flexible individual with a proven track record of successfully managing multiple tasks and priorities within a fast-paced environment with minimal oversight.
  • Excellent project management skills.
  • Great attention to detail with excellent interpersonal, organizational, written and verbal communication skills.
  • Proficiency in EDC systems (i.e. Medidata Rave) and other integrated clinical systems (e.g., IxRS/IRT).
  • Working knowledge of ICH GCP and other regulatory guidance documents.
  • Working knowledge of CDISC/CDASH, GCDMP and other clinical data standards.

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