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Clinical Data Assistant Jobs in Silver Spring, MD

Collaborate with clinical research staff to understand protocol requirements and ensure data management activities support study objectives. * Assist with the development, implementation, and ...

Description Clinical Data & Applications Analyst Position Summary CRi is seeking a Clinical Data ... * Assist with research and evaluation of emerging technologies that may improve clinical ...

Enter, verify, and reconcile clinical data within electronic research systems. * Monitor study timelines and assist with tracking project deliverables. * Communicate effectively with investigators ...

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Clinical Data Assistant information

What is a clinical data assistant?

Clinical Data Assistants are professionals who support the collection, management, and analysis of clinical data in healthcare and research settings. They ensure that data from clinical trials or medical records are accurately recorded, organized, and compliant with regulatory standards. Their work is crucial for maintaining data integrity and supporting the research process, often involving data entry, validation, and quality control tasks. Clinical Data Assistants collaborate with clinical teams, data managers, and other stakeholders to facilitate smooth data flow and support clinical research objectives.

What are some typical challenges a clinical data assistant might face when managing large volumes of clinical trial data?

Clinical Data Assistants often encounter challenges such as ensuring data accuracy while handling large datasets, dealing with incomplete or inconsistent information from various sources, and adhering to strict regulatory guidelines. They must be diligent in data entry, verification, and resolving discrepancies, often collaborating closely with clinical research coordinators and data managers. Effective communication and attention to detail are essential to maintain high data quality and support the overall success of clinical trials.

What are the key skills and qualifications needed to thrive as a clinical data assistant, and why are they important?

To excel as a Clinical Data Assistant, you need a solid understanding of data management, attention to detail, and familiarity with clinical research processes, typically supported by a degree in a health or life science field. Proficiency in electronic data capture (EDC) systems, Microsoft Excel, and knowledge of Good Clinical Practice (GCP) guidelines or relevant certifications are typical requirements. Strong organizational skills, communication, and the ability to work collaboratively within multidisciplinary teams make candidates stand out. These competencies are crucial for ensuring accurate data collection, regulatory compliance, and smooth execution of clinical studies.

What is the difference between Clinical Data Assistant vs Clinical Data Coordinator?

AspectClinical Data AssistantClinical Data Coordinator
CertificationsOften requires basic data management or healthcare certificationsTypically requires similar certifications, with additional experience
Work EnvironmentHospitals, clinics, research labsResearch institutions, hospitals, clinical trial sites
Job ResponsibilitiesData entry, data cleaning, supporting data collectionOverseeing data quality, managing databases, coordinating data flow

The Clinical Data Assistant primarily handles data entry and support tasks, while the Clinical Data Coordinator manages data quality and oversees data management processes. Both roles are essential in clinical research settings and often require similar certifications and work environments.

What are the most commonly searched types of Clinical Data jobs in Silver Spring, MD?

The most popular types of Clinical Data jobs in Silver Spring, MD are:

What are popular job titles related to Clinical Data Assistant jobs in Silver Spring, MD?

For Clinical Data Assistant jobs in Silver Spring, MD, the most frequently searched job titles are:

What cities near Silver Spring, MD are hiring for Clinical Data Assistant jobs?

Cities near Silver Spring, MD with the most Clinical Data Assistant job openings:

Infographic showing various Clinical Data Assistant job openings in Silver Spring, MD as of August 2026, with employment types broken down into 1% As Needed, 80% Full Time, 15% Part Time, and 4% Contract. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution.

Clinical Data Manager

Peers & Partners Inc

Bethesda, MD โ€ข On-site

Full-time

Posted 8 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.