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Associate Clinical Data Manager Jobs (NOW HIRING)

CDMs will provide comprehensive data management support to clinical research teams and contribute directly to the quality, integrity, and usability of clinical research data. In addition, CDMs will ...

MN

$45 - $47/hr

Clinical Data Manager Location: Maple Grove, MN Duration: 7 Months 100% Onsite Summary: The Clinical Data Manager is responsible for managing the development, documentation, and execution of risk ...

Clinical Data Manager Location: Maple Grove, MN Duration: 7 Months 100% Onsite Summary: The Clinical Data Manager is responsible for managing the development, documentation, and execution of risk ...

Clinical Data Manager Location: Irvine, CA USA 92618 Duration: 12 months (Strong Possibility of Extension) Employment Type: W2 Contingent Worker SUMMARY OF POSITION: As a key member of the Global ...

... as Clinical Data Manager to participate in and lead laboratory data operations to assess the ... Associate's degree * Two years of relevant research experience. Completion of the DOCR North ...

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams, external partners, and vendors to design, configure, and test clinical database systems, conduct data ...

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams, external partners, and vendors to design, configure, and test clinical database systems, conduct data ...

Clinical Data Manager

New York, NY · On-site

$115K - $145K/yr

About the Role We are looking for a Clinical Data Manager to accelerate Novellia's data curation and delivery processes. In this role, you will be responsible for working with a team of cross ...

ZS is seeking a Tech Project Delivery Manager to lead a high-velocity team focused on the future of Biometrics and Clinical Data. We are looking for a delivery leader who excels at navigating the ...

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Associate Clinical Data Manager information

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How much do associate clinical data manager jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for associate clinical data manager 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 does an associate clinical data manager do?

An Associate Clinical Data Manager is responsible for collecting, cleaning, and managing clinical trial data to ensure its accuracy, integrity, and compliance with regulatory standards. They work closely with clinical teams to design data collection tools, monitor data quality, and resolve discrepancies. Their work is crucial in supporting the analysis and reporting of clinical trial results, which can impact decisions about new medical treatments.

What are the key skills and qualifications needed to thrive as an associate clinical data manager?

To thrive as an Associate Clinical Data Manager, you need a solid background in life sciences or related fields, strong analytical abilities, and attention to detail, often supported by a relevant bachelor's degree. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools like Medidata Rave, and an understanding of regulatory guidelines such as ICH-GCP are typically required. Excellent organizational skills, effective communication, and problem-solving abilities help you excel in managing complex datasets and collaborating across teams. These skills ensure data integrity, regulatory compliance, and smooth conduct of clinical trials, which are critical to successful drug development.

What are some common challenges an associate clinical data manager might face when working on multi-site clinical trials?

Associate Clinical Data Managers often encounter challenges such as ensuring data consistency across different trial sites and managing discrepancies that arise from varying data entry practices. Coordinating with site staff, monitoring data quality, and adhering to strict timelines require strong communication and organizational skills. Additionally, adapting to evolving regulatory requirements and new data management technologies can be demanding, but these challenges also offer valuable learning opportunities for career growth.
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Infographic showing various Associate Clinical Data Manager job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $81,020 per year, or $39 per hour.

Clinical Data Manager

Peers and Partners

Bethesda, MD • On-site

Full-time

Posted 10 days ago


Job description

Position Overview
Peers and Partners, Inc. is seeking qualified Clinical Data Managers (CDMs) to support a major clinical research data management program at the National Institutes of Health (NIH). We are seeking candidates who can contribute immediately to a high-performing clinical research data management team while demonstrating the professionalism, judgment, technical capabilities, and attention to detail. CDMs will provide comprehensive data management support to clinical research teams and contribute directly to the quality, integrity, and usability of clinical research data. In addition, CDMs will work collaboratively with Federal clinical research personnel, investigators, research teams, and other contractor staff. Depending on program needs, CDMs may be assigned to specific clinical protocols, research areas, or research teams. The ideal candidate will have experience managing clinical or healthcare-related data and be comfortable working in a highly regulated, collaborative clinical research environment.
Key Responsibilities
  • Provide comprehensive clinical data management support to assigned clinical research protocols and research teams.
  • Review, organize, maintain, and manage clinical research data in accordance with established protocols, standard operating procedures (SOPs), and applicable Federal requirements.
  • Support data collection, data entry, data validation, data cleaning, data reconciliation, and quality assurance activities.
  • Review clinical research data for completeness, accuracy, consistency, and compliance with protocol requirements.
  • Identify data discrepancies, inconsistencies, missing information, and potential data quality issues and coordinate appropriate resolution.
  • Utilize current and legacy clinical research databases and other data management systems as required.
  • Support database maintenance, data queries, data tracking, and reporting activities.
  • Collaborate with clinical research staff to understand protocol requirements and ensure data management activities support study objectives.
  • Assist with the development, implementation, and maintenance of data management processes and procedures.
  • Maintain appropriate documentation of data management activities in accordance with SOPs and regulatory requirements.
  • Support quality assurance and quality control activities related to clinical research data.
  • Protect the confidentiality, integrity, and security of clinical research information.
  • Communicate effectively with Federal employees, investigators, clinical research staff, and other contractor personnel.
  • Work independently while also functioning effectively as part of multidisciplinary clinical research teams.
  • Adapt to multiple protocols, research areas, databases, and evolving program requirements.
  • Perform other data management activities as assigned by program leadership.

Required Qualifications
  • Bachelor's degree from an accredited college or university.
  • At least 3 years of relevant professional experience is preferred; however, recent college graduates with relevant clinical, healthcare, research, database, analytics, or data management experience will be considered.
  • Demonstrated experience working with data management, data quality, database, research, healthcare, or clinical research activities.
  • Strong attention to detail and ability to identify data discrepancies and inconsistencies.
  • Ability to manage multiple assignments and prioritize work in a deadline-driven environment.
  • Strong written and verbal communication skills.
  • Ability to work collaboratively with clinical research personnel and multidisciplinary teams.
  • Ability to work onsite at the NIH Main Campus in Bethesda, Maryland, up to five days per week.
  • Ability to maintain professionalism when interacting with Federal government personnel, investigators, researchers, and other contractor staff.

Education and Experience
  • Minimum Education: Bachelor's degree from an accredited college or university.
  • 3+ years of relevant experience preferred. Recent college graduates with relevant data management, healthcare, research, database, analytics, or clinical research experience may be considered.
  • Healthcare/Clinical Research Experience: Preferred.

Preferred Qualifications
  • Experience working in a healthcare, hospital, academic medical center, clinical research, or biomedical research environment.
  • Prior experience supporting NIH or another Federal health agency.
  • Experience supporting clinical trials, clinical protocols, or human-subjects research.
  • Experience with clinical research databases or electronic data capture systems.
  • Experience with data validation, data cleaning, quality control, or quality assurance.
  • Familiarity with clinical research documentation, SOPs, regulatory requirements, or Federal research requirements.
  • Experience working with legacy databases or transitioning/migrating data between systems.
  • Experience working directly with physicians, investigators, research coordinators, nurses, or other clinical research personnel.
  • Knowledge of clinical research data standards and data management best practices.

What We Are Looking For
Successful candidates will demonstrate:
  • Clinical research orientation: Understands the importance of accurate, complete, and reliable data to clinical research.
  • Data quality mindset: Naturally identifies discrepancies, missing information, inconsistencies, and potential quality issues.
  • Attention to detail: Able to work accurately with large volumes of information and maintain meticulous documentation.
  • Collaboration: Comfortable working closely with investigators, clinical research staff, Federal employees, and contractor personnel.
  • Professionalism: Demonstrates maturity and professionalism in a highly visible Federal clinical research environment.
  • Adaptability: Can learn new databases, protocols, systems, and processes quickly.
  • Accountability: Takes ownership of assigned work and follows established SOPs and quality requirements.