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Junior Clinical Data Manager Jobs in Reston, VA (NOW HIRING)

Pwc

Data Validation Risk - Manager

Washington, DC · On-site

$99K - $232K/yr

... junior staff. You are accountable for confirming project success and maintaining standards ... Responsibilities - Leading data validation and risk management initiatives to support client ...

MacroSys, LLC

Junior Data Analyst

Washington, DC · Remote

$50K - $55K/yr

We are currently seeking a full-time Junior Data Analyst to join our dynamic and purpose-driven ... Preferred but not required: familiarity with Jira or similar project management tools * Must be ...

OBAN Corporation

Data Analyst (Jr.)

Vienna, VA · On-site

Junior Data Analyst Disclaimer: This position is being recruited in support of potential future ... strategic, and tactical management solutions to public and private sector clients. OBAN ...

OBAN Corporation

Data Analyst (Jr.)

Vienna, VA · On-site

Junior Data Analyst Disclaimer: This position is being recruited in support of potential future ... strategic, and tactical management solutions to public and private sector clients. OBAN ...

ASM Research

Data Analyst Junior

Fairfax, VA · On-site

Position Overview The Junior Data Analyst supports data-driven decision-making by leveraging an ... management decisions. We affirm our commitment to these fundamental policies. All recruiting ...

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Junior Clinical Data Manager information

See Reston, VA salary details

$19.8K

$54.6K

$91.6K

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

As of Aug 17, 2026, the average yearly pay for junior clinical data manager in Reston, VA is $54,579.00, according to ZipRecruiter salary data. Most workers in this role earn between $37,500.00 and $59,800.00 per year, depending on experience, location, and employer.

What does a junior clinical data manager do?

A Junior Clinical Data Manager is responsible for supporting the collection, management, and quality control of clinical trial data. They assist in designing data collection tools, verifying data accuracy, and ensuring compliance with regulatory standards. Their role often includes data entry oversight, query management, and collaboration with clinical research teams to resolve data discrepancies. Junior Clinical Data Managers help ensure that clinical trial data is reliable, secure, and ready for statistical analysis.

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

To thrive as a Junior Clinical Data Manager, you need a background in life sciences or related fields, strong analytical skills, and an understanding of clinical trial processes. Familiarity with data management systems such as EDC (Electronic Data Capture), CDMS (Clinical Data Management Systems), and knowledge of GCP (Good Clinical Practice) guidelines or certifications like CDM are important. Attention to detail, problem-solving abilities, and effective communication help ensure data quality and facilitate teamwork. These skills are crucial for maintaining data integrity, supporting regulatory compliance, and contributing to successful clinical research outcomes.

What are some typical challenges a junior clinical data manager may encounter when handling clinical trial data?

As a Junior Clinical Data Manager, one common challenge is ensuring data accuracy and consistency across multiple sources and formats, which requires strong attention to detail and effective communication with clinical teams. You may also face tight timelines for data cleaning and query resolution during critical trial phases. Collaborating with cross-functional teams, such as clinical research associates and biostatisticians, is essential for resolving discrepancies and maintaining data integrity throughout the study. Developing proficiency in data management systems and understanding regulatory requirements are key to overcoming these challenges and advancing in the role.

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

AspectJunior Clinical Data ManagerClinical Data Coordinator
Required CredentialsBachelor's degree in life sciences or related field; some roles may require certificationBachelor's degree; certification is a plus but not always required
Work EnvironmentTypically in clinical research teams, handling data management tasksSupports data collection and entry, often working closely with data managers
Employer & Industry UsagePharmaceutical companies, CROs, biotech firmsResearch sites, hospitals, CROs

The Junior Clinical Data Manager focuses on managing and validating clinical trial data, while the Clinical Data Coordinator primarily handles data entry and collection. Both roles require similar educational backgrounds, but the data manager has more responsibility for data quality and analysis.

What are popular job titles related to Junior Clinical Data Manager jobs in Reston, VA?

For Junior Clinical Data Manager jobs in Reston, VA, the most frequently searched job titles are:

What job categories do people searching Junior Clinical Data Manager jobs in Reston, VA look for?

The top searched job categories for Junior Clinical Data Manager jobs in Reston, VA are:

What cities near Reston, VA are hiring for Junior Clinical Data Manager jobs?

Cities near Reston, VA with the most Junior Clinical Data Manager job openings:

Junior Clinical Data Manager jobs near you
Infographic showing various Junior Clinical Data Manager job openings in Reston, VA as of August 2026, with employment types broken down into 88% Full Time, 11% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution, with an average salary of $54,579 per year, or $26.2 per hour.

Sr. Clinical Trial Protocol Coordinator at Kelly in Bethesda, Maryland

Disabledperson, Inc

Bethesda, MD • On-site

Other

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

Senior Clinical Trial Protocol Coordinator

Kelly Government Solutions is a strategic supplier and business partner to the federal government and its key suppliers. We are seeking a Senior Clinical Trial Protocol Coordinator to work on-site with the Vaccine Research Center at the National Institute of Allergy and Infectious Diseases (NIAID)/National Institutes of Health (NIH) in Bethesda, MD. This is a long-term contract position which offers:

  • Competitive compensation and comprehensive benefit package
  • Optional health, vision, and dental plans
  • Paid leave, paid federal holidays, and 401K plan.
  • Access to NIH's unparalleled resources and niche scientific initiatives
Key Tasks

(1) Assist Principal Investigators in the planning, development, and implementation of clinical protocols for evaluation of Vaccine Research Center investigational vaccine and monoclonal antibody products.

(2) Ensure that clinical research protocols, consent forms, Investigator Brochures and other clinical research documents are in compliance with applicable regulatory requirements defined by the Code of Federal Regulations (CFR) and Good Clinical Practice guidelines.

(3) Ensure that data collection plans are consistent with applicable regulatory requirements and the protocol objectives.

(4) Assist in protocol training, study implementation, site management and reporting of study outcomes.

(5) Design, write and develop documents related to the use of investigational products, including but not limited to: conducting background research, reviewing and interpreting scientific and technical information, technical writing, ensuring compliance with regulatory requirements, and preparing or editing scientific summaries, presentations and publications.

(6) Prepare and review regulatory submissions, annual reports, IND safety reports, human subjects experience sections for investigator brochures and other supporting documents for vaccine and other related product types.

(7) Manage protocol and trial development by working and coordinating with clinical research teams that include physicians, laboratory scientists, research nurses, pharmacists, regulatory personnel, and support staff.

(8) Manage clinical trial activities and communications with study team member throughout the protocol life cycle.

(9) Use systems for data management and document control, support the dissemination of information on vaccine, monoclonal antibody and other clinical trials and coordinate response to related inquiries from sites, sponsors, FDA, and other regulatory agencies.

(10) Assist with quality management activities for the Program by reviewing and developing policies and procedures and provide support to risk assessment and clinical monitoring activities.

(11) Design and conduct assessments of quality management and regulatory performance with respect to the achievement of program goals and objectives.

Key Requirements

(1) Master's degree in Life Sciences or related discipline. Two years of specialized experience plus a bachelor's degree is equivalent.

(2) Minimum of two (2) years of clinical research experience. Expertise in the fundamentals of clinical trials including protocol development, clinical research policies and procedures, clinical data management, and database operations and analysis. Familiarity with IRB requirements and related regulatory requirements.

(3) Ability to review, collect, assess and summarize scientific and other complex data and information related to the development of investigational products.

(4) Knowledge of tools and software such as MS Word, clinical data management systems, medical publication databases, document control systems, and other information systems that support clinical research.

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