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Clinical Research Data Manager Jobs in Silver Spring, MD

Prism Vision Group

Clinical Research Assistant

Fairfax, VA · On-site

$46K - $96K/yr

Clinical Safety Data Management, 21 CFR, and has IATA certification * Travels to investigator meetings * Participates in weekly meetings with the research team, provides study metrics * Responds to ...

Ambu

Clinical Data Manager

Columbia, MD · On-site

Clinical Research Department: Clinical Affairs Employment Type: Full-time Req ID: 10220 Job Title: Clinical Data Manager Reports to: Director, Clinical Data Acquisition Location: Remote or Columbia ...

Cape Fox SS

Research Nurse

Baltimore, MD · On-site

$45 - $50/hr

... data from these and other sources Manage clinical and research support activities to ensure patient safety and address the clinical needs of the patients Administers protocol consents and ...

Axle

Temporary - Clinical Research Coordinator

Baltimore, MD · On-site

$24 - $32/hr

Instruct data entry and clinical staff in procedures relative to data management, protocol ... Mentor new clinical research coordinators on all aspects of research support. Disclaimer: The above ...

Axle

Temporary - Clinical Research Coordinator

Baltimore, MD · On-site

$24 - $32/hr

Instruct data entry and clinical staff in procedures relative to data management, protocol ... Mentor new clinical research coordinators on all aspects of research support. Disclaimer: The above ...

A-Team Solutions

RESEARCH NURSE

Bethesda, MD · On-site

$100K - $135K/yr

Manage clinical research data and support data quality assurance. Required Skills/Background: * Degree from a professional nursing program approved by the legally designated State accrediting agency ...

CENTER FOR DERMATOLOGY

Be Seen First

Clinical Research Coordinator

Washington, DC · On-site

$62K - $82K/yr

Manage data collection, entry, and management using electronic medical record (EMR) systems and ... Proven supervising experience in a clinical research setting or related healthcare environment

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All JobsClinical Research Data JobsClinical Research Data Manager JobsClinical Research Data Manager Jobs in Silver Spring, MD

Clinical Research Data Manager information

See Silver Spring, MD salary details

$50.7K

$111K

$195.4K

How much do clinical research data manager jobs pay per year?

As of Aug 18, 2026, the average yearly pay for clinical research data manager in Silver Spring, MD is $110,962.00, according to ZipRecruiter salary data. Most workers in this role earn between $83,700.00 and $126,600.00 per year, depending on experience, location, and employer.

What is a clinical research data manager?

A Clinical Research Data Manager is a professional responsible for collecting, organizing, and managing the data generated during clinical trials and research studies. They ensure that the data is accurate, complete, and complies with regulatory standards. Their work is crucial for the integrity of clinical research, as it allows researchers to draw valid conclusions from the study. Data managers work closely with clinical teams, statisticians, and regulatory bodies to maintain high-quality data throughout the research process.

What are some common challenges faced by clinical research data managers during multi-site trials?

Clinical Research Data Managers often encounter challenges coordinating data collection across multiple research sites, such as ensuring consistent data entry, handling discrepancies, and maintaining data quality standards. Effective communication with site staff and timely resolution of data queries are essential to minimize delays and errors. Utilizing robust electronic data capture (EDC) systems and standardized procedures helps, but proactive problem-solving and attention to detail remain crucial for success in this role.

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

To thrive as a Clinical Research Data Manager, you need a solid background in life sciences, data management principles, and experience with clinical trial processes, often backed by a relevant bachelor's degree. Proficiency in electronic data capture (EDC) systems, database management tools like SQL, and familiarity with regulatory standards such as GCP are essential. Strong attention to detail, problem-solving abilities, and effective communication skills help ensure data integrity and smooth collaboration across research teams. These skills are crucial for maintaining high-quality, compliant data that support successful clinical trials and regulatory submissions.

What is the difference between Clinical Research Data Manager vs Clinical Research Coordinator?

AspectClinical Research Data ManagerClinical Research Coordinator
Primary RoleOversees data collection, management, and quality control of clinical trial data.Coordinates daily trial activities, patient recruitment, and site management.
Required SkillsData management, database systems, regulatory compliance.Patient interaction, study protocol adherence, site coordination.
Work EnvironmentData centers, clinical trial sites, research organizations.Clinical sites, hospitals, research facilities.
Common CertificationsCDMP, SAS, or related data management certifications.GCP certification, clinical trial training.

While both roles support clinical research, the Clinical Research Data Manager focuses on data integrity and management, whereas the Clinical Research Coordinator handles trial operations and participant coordination. Understanding these differences helps in choosing the right career path or job search focus.

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

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

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

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

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The top searched job categories for Clinical Research Data Manager jobs in Silver Spring, MD are:

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

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

Clinical Research Data Manager jobs near you
Infographic showing various Clinical Research Data Manager job openings in Silver Spring, MD as of August 2026, with employment types broken down into 90% Full Time, 9% Part Time, and 1% Contract. Highlights an 81% Physical, 2% Hybrid, and 17% Remote job distribution, with an average salary of $110,962 per year, or $53.3 per hour.

Clinical Research Assistant

Prism Vision Group

Fairfax, VA • On-site

$46K - $96K/yr

Full-time

Posted 5 days ago

PRISM Vision Group rating

7.2

Company rating: 7.2 out of 10

Based on 15 frontline employees who took The Breakroom Quiz

Job description

This exempt, onsite role is located at Retina Group of Washington, Fairfax, VA location, which is part of Prism Vision Group.

Compensation Range: $46,675.20 - $96,969.60/annual (Dependent on Experience)

The Clinical Research Assistant reports to the RGW Office Manager and RGW Research Lead and will aid in the coordination and conduct of research under the supervision of a designated physician. The Clinical Research Assistant will perform a variety of duties involved in the collection, compilation, documentation and analysis of clinical research data. The Clinical Research Assistant will develop knowledge of the research studies, rationale, subjects and procedures associated with the studies as designated by the Senior/Lead Clinical Research Coordinator. This  position is designed specifically to develop into a Clinical Research Coordinator and travels between multiple locations as needed.

Role and Responsibilities:

  • Assists in recruitment efforts to screen potential patients for eligibility for studies.
  • Obtains informed consent from patients and conducts study visits for clinical trials
  • Creates Case Report Forms
  • Completes assessments on study subjects as per protocol
  • Documents study assessments
  • Enters study data into EDC systems
  • Collects, processes, stores and shipslab specimens; documents lab procedures, lab results and follows up with patients and medical staff as necessary
  • Coordinates, monitors visits with CRAs for each trial to ensure accurate documentation; makes corrections to data as necessary
  • Assists during Sponsor and FDA audits
  • Responsible for submissions and reports to the IRB; maintains documentation of IRB communications and decisions
  • Documents adverse events and notifies PI, sponsor and IRB under CRC guidance
  • Assumes test article accountability
  • Possesses a sound and in-depth understanding of each protocol that has been assigned as a primary responsibility
  • Maintains compliance with Good Clinical Practice; Clinical Safety Data Management, 21 CFR, and has IATA certification
  • Travels to investigator meetings
  • Participates in weekly meetings with the research team, provides study metrics
  • Responds to requests in a timely manner, gives/receives correct information, encourages dialogue and follow-through, secures accurate signatures, maintains files in an organized and up-to-date manner

Qualifications:

Education: Associates or Bachelors Degree preferred in Science or related field. Equivalent relevant experience and/or training in lieu of education is acceptable.

Experience: 1+ years’ relevant experience (e.g. research, clinical, interaction with study population, program coordination)

Knowledge/Skills/Experience:

• Excellent Excel, Word, PowerPoint and reporting skills

• Excellent interpersonal skills to deal effectively with patients, physicians, clinicians and administrators

• Excellent organizational skills and self-management skills to independently manage workflow

• Ability to prioritize

• Meticulous attention to detail

• Knowledge of medical terminology

• Knowledge of good clinical practice, FDA, OHRP, HIPAA policies

• Experience using Microsoft Office Suite

• Certification through either ACRP or SoCRA highly preferred

Qualifications:

Qualifications:

Education: Associates or Bachelors Degree preferred in Science or related field. Equivalent relevant experience and/or training in lieu of education is acceptable.

Experience: 1+ years’ relevant experience (e.g. research, clinical, interaction with study population, program coordination)

Knowledge/Skills/Experience:

• Excellent Excel, Word, PowerPoint and reporting skills

• Excellent interpersonal skills to deal effectively with patients, physicians, clinicians and administrators

• Excellent organizational skills and self-management skills to independently manage workflow

• Ability to prioritize

• Meticulous attention to detail

• Knowledge of medical terminology

• Knowledge of good clinical practice, FDA, OHRP, HIPAA policies

• Experience using Microsoft Office Suite

• Certification through either ACRP or SoCRA highly preferred

Education:UNAVAILABLEEmployment Type: FULL_TIME

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