ZipRecruiter

Log In

1

Associate Director Clinical Data Management Jobs

next page

Showing results 1-20

All JobsAssociate Clinical Data Management JobsAssociate Director Clinical Data Management Jobs

Associate Director Clinical Data Management information

See salary details

$13

$38

$86

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

As of Sep 2, 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 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.

More about Associate Director Clinical Data Management jobs

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

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

What states have the most Associate Director Clinical Data Management jobs?

States with the most job openings for Associate Director Clinical Data Management jobs include:

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

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

Associate Director Clinical Data Management jobs near you
Infographic showing various Associate Director Clinical Data Management job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 89% Physical, 2% Hybrid, and 9% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.

Associate Director, Clinical Data Management

Corcept Therapeutics

Redwood City, CA

$229K - $269K/yr

Full-time

Re-posted 5 days ago

Job description

The Associate Director, Clinical Data Management ensures optimized data collection, flow and access across EDC and non-EDC data sources. Responsible for accuracy, completeness and CDISC compliance of Corcept clinical databases.

 Responsibilities:

  • Works in cooperation with Director of Clinical Data Management to select and maintain preferred vendor network for data management activities
  • Reviews, proposes and obtains bids for tools enabling real-time data visualization, interrogation, and reporting
  • Manages strategic input into the design of data flow across EDC and non-EDC data sources across vendor network
  • Manages data management service providers to ensure the quality of deliverables and that timelines are met
  • Develops and contributes to the design of processes enabling near-real-time data access for Corcept clinical trials
  • Ensure data quality of clinical database through implementation of CDISC compliance
  • Reviews and critically assesses data query resolution metrics and suggests process improvement
  • Reviews study protocols to ensure that data collection and CRF design meet study objectives
  • Manages and oversees SAE reconciliation between clinical and pharmacovigilance database
  • Review clinical data for completeness, accuracy, and consistency in accordance with the investigational plan
  • Provide subject matter expertise to project team members during all phases of project life cycle
  • Provides accurate and timely clinical data to internal and external customers upon request
  • Manage development, test, and maintain data management systems
  • Manage development and periodic review of Data Management specific SOPs, WIs and templates
  • Provide subject matter expertise prior, during, and post internal and external audits and inspections
  • Maintain compliance with company and study-specific learning requirements

Preferred Skills, Qualifications or Technical Proficiencies:

  • Master's Degree in health care or life sciences preferred
  • Relational database experience, SQL, SAS, and clinical data management systems
  • Knowledge and experience with MedDRA, WHODrug and other Thesaurus classification of controlled management systems
  • Knowledge of CDISC/SDTM. Hands-on experience preferred
  • Hands-on experience working with mainstream EDC systems (e.g. Rave, Medrio, Inform)
  • Familiarity with Data Visualization Tools for quick customized data access (e.g Spotfire, Tableau, RShiny)
  • In-depth understanding of Data Management regulatory guidelines: ICH, GCDMP, 21CFR Part 11
  • Demonstrated strong management abilities for project and staff management of Data Management Deliverables in clinical development

Preferred Education and Experience:

  • Bachelors or higher in science, math or computer science
  • 10+ year experience in clinical trial industry (med device, pharma or biotech)
  • 10+ year experience in data management in clinical trial industry (med device, pharma or biotech)
  • Minimum of 3 years experience in preparing, executing, and finalizing Medical Coding (MedDRA and WHODrug) within the Medidata Rave Coder system
  • Strong knowledge of the MedDRA and WHODrug dictionaries along with their uprevisions
  • Experience in IT-related field a plus
  • Experience with Endocrinology clinical trials and CDISC therapeutic area standards
  • Experience with management of data flow and curation of biomarker data a plus
  • Experience managing Data Management CROs
  • Direct report management and oversight

The pay range that the Company reasonably expects to pay for this headquarters-based position is $229,300 - $269,800; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education.

 Applicants must be currently authorized to work in the United States on a full-time basis.

Apply