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Assistant Research Manager Jobs in Virginia (NOW HIRING)

Research Assistant

Quantico, VA ยท On-site

$20.75 - $28.50/hr

Manage data entry and ensure the accuracy and integrity of data collected throughout the research ... used. * Assist with statistical analysis, using software tools to interpret data and generate ...

Research Assistant

Quantico, VA

$20.75 - $28.50/hr

Manage data entry and ensure the accuracy and integrity of data collected throughout the research ... used. * Assist with statistical analysis, using software tools to interpret data and generate ...

Research Assistant

Blacksburg, VA

$17 - $23.25/hr

Research Assistant Apply now Back to search results Job no: 533999 Work type ... Staff Senior management: Vice President for Research Department: Fralin Biomedical Res. Institute ...

Research Assistant

Blacksburg, VA

$17 - $23.25/hr

Research Assistant Apply now Back to search results Job no: 535375 Work type ... Staff Senior management: Vice President for Research Department: Fralin Biomedical Res. Institute ...

Research Assistant

Hampton, VA ยท On-site

$18.75 - $25.75/hr

... Manager, this position will perform research and data entry, export and organize data, prepare ... assist with general data analysis to support department operations and accreditation efforts. If ...

Research Assistant

Fairfax, VA ยท On-site

$19 - $26.25/hr

... research. Collects data from initial patient contact through course of therapy and long-term ... data management functions for the department. May assist with direct patient care, laboratory ...

Lead, User Intelligence Research

Mclean, VA ยท Hybrid

$168K/yr

Lead, User Intelligence Research Lead, User Intelligence Research Manager ( Individual contributor ... specific UX metrics. Assist in developing mechanisms to collect/measure UX metrics, conduct ...

Research Assistant Apply now Back to search results Job no: 534078 Work type ... Hourly Wage/Part-Time Senior management: College of Veterinary Medicine Department: Biomedical ...

Lead, User Intelligence Research

Richmond, VA ยท Hybrid

$165K/yr

Lead, User Intelligence Research Lead, User Intelligence Research Manager ( Individual contributor ... specific UX metrics. Assist in developing mechanisms to collect/measure UX metrics, conduct ...

Research Assistant

Hampton, VA ยท On-site

$18.82/hr

... Manager, this position will perform research and data entry, export and organize data, prepare ... assist with general data analysis to support department operations and accreditation efforts. If ...

Research Assistant - MCU/CDET

Quantico, VA ยท On-site

$20.75 - $28.50/hr

Manage data entry and ensure the accuracy and integrity of data collected throughout the research ... used. * Assist with statistical analysis using software tools to interpret data and generate ...

Showing results 21-40

Assistant Research Manager information

What are the key skills and qualifications needed to thrive as an assistant research manager?

To thrive as an Assistant Research Manager, you need strong analytical abilities, project management expertise, and a relevant degree such as in marketing, social sciences, or business. Familiarity with statistical analysis software (like SPSS or R), data visualization tools, and experience in survey methodologies or research platforms is typically required. Excellent communication, leadership, and problem-solving skills help you coordinate teams and interpret complex findings for stakeholders. These skills ensure accurate research outcomes, efficient project execution, and effective collaboration within research teams and with clients.

What are some common challenges faced by assistant research managers, and how can they effectively address them?

Assistant Research Managers often encounter challenges such as balancing multiple projects with tight deadlines, ensuring data accuracy, and coordinating communication among various stakeholders. To address these, it's important to develop strong organizational skills, utilize project management tools, and foster clear communication with research teams and clients. Proactively identifying potential bottlenecks and regularly updating stakeholders can help maintain project momentum and improve overall efficiency.

What is the difference between Assistant Research Manager vs Research Analyst?

AspectAssistant Research ManagerResearch Analyst
Required CredentialsBachelor's or Master's in relevant field, some managerial experienceBachelor's or Master's in related field, strong analytical skills
Work EnvironmentSupports research projects, collaborates with teams, may assist in managing staffConducts data analysis, prepares reports, supports research initiatives
Employer & Industry UsageUsed in corporate, academic, and market research settingsCommon in market research, consulting, and academic research

The Assistant Research Manager typically has some managerial responsibilities and oversees research projects, while the Research Analyst focuses on data analysis and report preparation. Both roles require strong research skills, but the Assistant Research Manager often supports team management and project coordination.

What are the most commonly searched types of Research Manager jobs in Virginia?

The most popular types of Research Manager jobs in Virginia are:

Infographic showing various Assistant Research Manager job openings in Virginia as of August 2026, with employment types broken down into 85% Full Time, 14% Part Time, and 1% Contract. Highlights an 84% Physical, 3% Hybrid, and 13% Remote job distribution.

Clincal Research Coordinator II/III

Arizona Arthritis & Rheumatology Associates

Fairfax, VA โ€ข On-site

$67K - $82K/yr

Full-time

Re-posted yesterday


Job description

Job Type
Full-time
Description
POSITION DESCRIPTION: The Clinical Research Coordinator II (CRC) reports to the Regional Research Manager and is responsible for coordinating and implementing assigned protocols in compliance with FDA CFR, GCP and company SOPs. The CRC collects and records clinical research data, assists in patient assessments, scheduling, maintain study files, study supplies and study medication accountability.
RESPONSIBILITIES:
  • Responsible for the coordination of observational and interventional clinical research trials assigned
  • Performance expectations will be assigned based on effort for each visit
  • Knowledge of all active protocols and disease indications within the company, and providing information about these protocols to staff and patients.
  • Responsible for the recruitment and screening of potential participants, which includes chart review of patients and schedules, contacting leads from outside recruitment efforts, and following up on referrals from all sources.
  • The CRC is responsible for meeting recruitment goals for each study. The methodology of recruitment will include, but is not limited to daily chart review, hosting recruitment breakfasts, advertising when funds are available, referrals from rheumatologists and other AARA staff and may include attending health fairs and community outreach.
  • Keeping the clinical trial management system updated with newly recruited subjects, tracking completed visits and stipends for the participants and investigators, and ensuring status of each patient is accurate.
  • Responsible for chain of custody and accurate accountability of investigation product and devices.
  • Plans, prepares and performs tasks required by protocol, which may include, but not limited to the following:
  • Informed Consent
  • Obtaining patient medical history and medication lists
  • Phlebotomy and basic laboratory tests
  • Processing & shipping labs for central and local labs
  • Patient education and training
  • ECG
  • Administer questionnaires and assessments
  • Vital signs
  • Collect information for adverse event reporting
  • Assist with joint counts and other efficacy assessments
  • Data Entry and Query Resolution
  • Study drug administration, including injections
  • Tracking study supply inventory and reordering when necessary
  • Schedule patient visits in appropriate electronic systems
  • Documenting all patient visits and communications in progress notes
  • Triages adverse events and communicates with the research physician regarding the occurrence of adverse events and serious adverse events within 24 hrs. Follow-up with the subject and collect required information.
  • Provides educational information to subjects. Serves as a resource and support person for subjects and families by being a consistent person they can contact within the clinical research program.
  • Ensures uniform implementation of protocols by completing required training documentation in a consistent, accurate and timely manner.
  • Assists in regulatory functions, including but not limited to preparing appropriate Institutional Review Board (IRB) forms, processing updated informed consents, protocols, correspondence, and regulatory filing in an accurate and timely manner.
  • Responsible for administrative duties including filing documents related to subjects' participation in research, regulatory, lab results, receipts, invoices, calibration reports, etc.
  • Serves as a liaison to all physicians, employees, and third-party vendors.
  • Participates in monitoring visits from sponsor provided appointees, ensures monitors can meet/speak with PI and ensures all concerns are addressed in a timely manner.
  • Ensure the delegation logs are correct and only delegated site staff are performing duties as listed on the delegation log for any given study.
  • Ensures that primary referring physicians receive timely progress notes on the patient's diagnosis and treatment.
  • May assume primary responsibility in the implementation and management of new clinical trials in a knowledgeable and collaborative manner.
  • Performs all functions according to established policies, procedures (SOPS), regulatory and accreditation requirements, federal and state regulations, good clinical practice, as well as applicable professional standards.
  • Provides all employees and research subjects with excellent service experience by consistently demonstrating professional decorum.
  • Maintaining office supply inventory while keeping an organized office space.
  • Travel as necessary for meetings and to assist other sites.

Requirements
Qualifications:
  • Bachelor's degree or equivalent
  • 1 year experience as a clinical research coordinator
  • Must have in-depth knowledge of medical procedures and clinical terminology
  • Possess strong organization and communication skills
  • Ability to develop and maintain strong professional relationships with all providers and research subjects
  • Excellent working knowledge of clinical research industry, ICH-GCP Guidelines and all federal regulations regarding clinical research.
  • Ability to lift 20 pounds
  • Willing and able to travel as needed to Rockville, White Oak and Frederick sites

Salary Description
67,000-82,744