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Associate Director Clinical Data Management Jobs

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Associate Director, Data Management

Job Summary The Associate Director, Data Management will be responsible for overseeing the start-up ... The individual will provide data management clinical development program leadership and will ...

MSD

Specialists, Clinical Data Management

West Point, PA · On-site

$87K - $137K/yr

Associate degree with a minimum of 3 years' experience working in clinical data programming, data engineering, or related data-management/clinical operations functions OR * Bachelor's Degree with a ...

Merck & Co.

Director, Program Lead, Clinical Data Management-Leads program-level strategy and execution across multiple programs or therapeutic areas, serving as the Global Clinical Data Management subject ...

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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.

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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 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 / Director, Clinical Development

Immunome, Inc.

Bothell, WA • On-site

$342K - $394K/yr

Full-time

Re-posted 19 days ago

Job description

Position Overview

We are seeking a highly motivated physician to join Immunome as Associate Director / Director, Clinical Development, supporting the development of our investigational oncology pipeline. This individual will provide medical and scientific oversight for clinical studies and serve as a key member of the Clinical Development team, partnering closely with Clinical Operations, Biostatistics, Data Management, Regulatory Affairs, Pharmacovigilance, Medical Writing, and Translational Sciences. 

The Associate Director/Director will be responsible for supporting protocol design and implementation, patient safety oversight, medical monitoring of ongoing trials, investigator and site engagement, medical review of emerging safety and efficacy data, and contribution to regulatory and scientific interactions. This position offers an opportunity to play a meaningful role in shaping the clinical development strategy for novel therapies addressing significant unmet needs in oncology. 

Responsibilities

  • Provide medical monitoring oversight for oncology clinical trials, including review of safety events, eligibility questions, dose modifications, protocol deviations, laboratory abnormalities, and emerging clinical data.  
  • Serve as the primary medical point of contact for investigators, study sites, CRO medical monitors, and internal cross-functional teams. 
  • Support safetymonitoringand pharmacovigilance activities, including review and medical input on adverse events, suspected unexpected serious adverse reactions, and other clinically significant safety findings. 
  • Collaboratewith internal and external stakeholders to design andimplementa clinical development plan across indications. 
  • Author key clinical trial documents and clinical sections of regulatory filings such as protocols, pre-INDs, IND/CTAs, Investigator Brochures, briefing documents, and BLAs. 
  • Collaborate cross-functionallywith clinical operations, regulatory, project management, manufacturing, and business development to define timelines, manage risks, and ensure milestone delivery. 
  • Work closely with translational sciences to integrate keybiomarkerand pharmacodynamic endpoints into clinical study designs. 
  • Establish andmaintainstrongrelationships with PIs,KOLs,and other external stakeholders. 
  • Review, assess, interpret,and communicate clinical trial data to internal stakeholders and external partners. 
  • Lead clinical trial data publication efforts. 
  • Lead or contribute to key external meetings such as advisory boards, safety review committees, investigatormeetings, and site trainings. 
  • Support quality initiatives related to clinical trial conduct,as needed. 

Qualifications

  • M.D., D.O., orequivalent. Board certification in medical oncologyorhematology preferred.  
  • A minimum of1year of experience in Clinical DevelopmentandPhase 1 - 3 oncology clinical trialsin a biotech or pharmaceutical setting, or equivalent. 

Knowledge and Skills

  • Proven experience advancing therapeutic programs in early or late-stage clinical development. 
  • Understanding of FDA and other health authority regulatory requirements and successfultrack recordin regulatory interactions. 
  • Demonstrated leadership and ability to effectively manage cross-functional teams. 
  • Excellent written and verbal communication skills, with the ability to communicate complex medical and scientific information clearly to diverse audiences. 
  • Strong organizational skills and ability to manage multiple studies, priorities, and timelines in a fast-paced biotech environment. 
  • High attention to detail, sound clinical judgment, and strong commitment to patient safety and data quality. 

Washington State Pay Range - Associate Director: $287,887 - $333,496 

Washington State Pay Range - Director: $342,540 - $394,941 

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