Top 179 Research Associate Jobs in Silver Spring, MD

Clinical Research Associate II
Emmes Group —Rockville, MD
- Full-time
- Remote
- Mid-level
- Bachelor's degree
- Organizational skills
Research Associate I - MRBD
Henry M. Jackson Foundation —Silver Spring, MD
- $52,800 - $65,000 a year
- Full-time
- Entry level
- Health insurance
- Dental insurance
6d
Research Associate
GeneCopoeia —Rockville, MD
- Email
- Microsoft Outlook
- Maintenance
- Research
Research Assistant/Associate - Junior Evaluator
MayaTech Corporation —Silver Spring, MD
- Full-time
- Master's degree
- Analysis skills
- Bachelor's degree
- Health insurance
In-House Clinical Research Associate
TECHNICAL RESOURCES INT'L —Bethesda, MD
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Writing skills
Clinical Research Associate
Georgetown University —Washington, DC
- $47,586.00 - $87,558.13 a year
- Full-time
- Patient monitoring
- 5 years
- Mid-level
- Disability insurance
- Health insurance
Research Associate II - Preventive Medicine & Biostatistics
Henry M. Jackson Foundation —Bethesda, MD
- $61,000 - $88,000 a year
- Full-time
- Hybrid work
- Mid-level
- University
- Commercial
- Health insurance
- Dental insurance
Research Assistant- Rockville
Maryland Treatment Centers, Inc. —Rockville, MD
- Full-time
- Vital signs
- Bachelor's degree
- Psychology
Quick Apply
In-House Clinical Research Associate
Technical Resources International, Inc. —Bethesda, MD
- $50,000 - $80,000 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Writing skills
Research Associate II
LGC Clinical Diagnostics —Gaithersburg, MD
- $27 - $37 an hour
- Full-time
- Mid-level
- Master's degree
- Analysis skills
- Health savings account
- Disability insurance
Quick Apply
6d
Research Associate I - Public Health Research - DC Hybrid Office
NORC at the University of Chicago —Washington, DC
- $56,000 a year
- Full-time
- Hybrid work
- Office
- Business development experience
- Analysis skills
- Paid parental leave
- Paid holidays
Research Associate
Institute for Defense Analyses —Alexandria, VA
- $68,681 - $194,054 a year
- Email
- Writing skills
- Master's degree
- Analysis skills
5d
Research Associate
Democratic National Committee —Washington, DC
- $54,100 a year
- Full-time
- Microsoft Word
- Microsoft Excel
- Writing skills
- Paid holidays
- Health insurance
Senior Research Associate
Meso Scale Diagnostics, LLC. —Gaithersburg, MD
- $67,900 - $101,000 a year
- Public speaking
- Mid-level
- Master's degree
- Paid parental leave
- AD&D insurance
Quick Apply
Senior Clean Energy Research Associate
Climate Power —Washington, DC
- $74,675 - $89,610 a year
- Weekends as needed
- Background check
- Google Workspace
- Mid-level
- Loan repayment program
- Health insurance
Quick Apply
Sr. Clinical Research Associate
Emmes Group —Rockville, MD
- Full-time
- Bachelor's degree
- Organizational skills
- Experience equivalent to degree accepted
Associate Research Scientist
Smithers PDS (Pharmaceutical Development Services) —Gaithersburg, MD
- $75,000 - $100,000 a year
- Extended hours
- Microsoft Word
- Bachelor of Science
- Mid-level
- Health insurance
- Dental insurance
Quick Apply
Clinical Research Assistant I - MED
Henry M. Jackson Foundation —Bethesda, MD
- $19.33 - $24.03 an hour
- Full-time
- Hybrid work
- Internal Medicine
- Entry level
- Health insurance
- Dental insurance
Research Associate
Hudson Institute —Washington, DC
- $52,000 - $56,000 a year
- Full-time
- Management
- Mid-level
- Office
- Commuter assistance
- Paid parental leave
Research Project Associate
Inova Health System —Fairfax, VA
- Full-time
- Administrative experience
- Children
- Associate's degree
- Wellness program
- Paid parental leave
8h

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Clinical Research Associate II

Emmes Group -
Rockville, MD

Apply Now

Job Details

Full-time

Qualifications

Project reporting
Data quality checks
Clinical study protocols and reports
Regulatory documents
Clinical compliance checks
Informed consent
Adverse event reporting
Operations coordination planning
Routine inspections
Mid-level
Clinical audit and monitoring
ICH guidelines
Clinical staff training
Bachelor's degree
Task prioritization
Clinical training
Scientific protocols
Team training
Data quality monitoring
Organizational skills
Clinical trial standard operating procedures
Clinical trial patient safety management
Document archiving
Document quality checks
Clinical research inspection readiness
Productivity software
Clinical quality assurance standards
Training & development
1 year
Clinical trial site selection

Full Job Description

Overview:

Clinical Research Associate II

Be Part of One Team, One Purpose.

At Emmes Group, we’re shaping the future of clinical research—where human intelligence meets cutting-edge technology to drive meaningful advancements in healthcare. With over 47 years of scientific excellence, we’ve led groundbreaking research in cell and gene therapy, vaccines, infectious diseases, ophthalmology, rare diseases, and neuroscience.

Through our two business units—Emmes, a full-service CRO, and Veridix AI, our technology, data, and analytical solutions —we are modernizing clinical trials and accelerating the development of life-changing therapies.

We believe that every clinical breakthrough starts with people—people who are passionate, purpose-driven, and ready to make an impact. At Emmes Group, we bring People, Science, and Technology together to collaborate with our customers and deliver global health impact. Our culture is built on integrity, collaboration, and innovation, ensuring that every challenge is met with perseverance and accountability.

The Clinical Research Associate (CRA) II is responsible for monitoring clinical study sites either onsite at investigative sites or remotely to ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH GCP, and all applicable regulatory requirements. The CRA will conduct monitoring visits and activities in accordance with Emmes SOPs, applicable regulations, and ICH GCP.

Responsibilities:

Under supervision of the project CRA staff oversight lead, example, Clinical Study Manager, Lead CRA, Project Manager, etc., independently schedules and conducts remote and on-site monitoring visits such as qualification pre study visits, site initiation visits, interim routine monitoring visits, closeout visits, and for cause visits.
As part of the site visits, independently conducts Informed Consent ICF review, source data verification source document review, review for compliance with required reporting tracking of adverse events and protocol deviations, investigator site file review, laboratory tour and specimen storage assessment, pharmacy Investigational Product IP Investigational Device ID storage location tour and storage condition assessment, IP ID accountability, facilities tours, and other activities per the site monitoring plan under minimal direction from the project CRA staff oversight lead.
Documents observations and monitoring activities in a site visit report at the conclusion of the visit.
Facilitates and oversees Action Item resolution post visit.
Helps to ensure that clinical sites are conducting the study in compliance with protocol clinical investigational plan, SOPs, ICH GCP, and other applicable regulations.
Provides training and retraining to site staff including protocol, GCP GDP, and other training under direction from the project CRA staff oversight lead.
Identifies areas requiring follow up and improvement at each clinical study site and reports findings to project CRA staff oversight lead.
Ensures all visits are conducted according to country regulations, ICH GCP, and company standard operating procedures
Serves as point of contact for study site personnel to answer questions and resolve studyrelated issues under the direction of the project CRA staff oversight lead.
May assist with the development and or review of study related materials including protocols, informed consent forms, monitoring plan, monitoring documents, etc.
Prepares for and attends project team meetings and provides updates on project status and site specific performance
Works collaboratively and effectively in a project team environment including internal and external colleagues to meet project objectives and timelines.
Participates in Investigator Meetings or other client meetings as needed.
Assists with filing and archiving of study documents.
Assists in preparing sites for audits and may provide support and cooperation during audits inspections including translation to Auditor if needed.
May assist with coordination of clinical study supplies.
May assist with submission of applications notifications to Institutional Review Board IRB Ethics Committee EC Regulatory Authority.
May assist with site recruitment oversight activities such as developing focused patient recruitment strategies and action plans.
Performs site management activities as required
Performs other duties as assigned
Complies with all policies and standards

Qualifications:

Bachelor's Degree Scientific discipline preferred or equivalent work experience Required
1-3 years 1-2 years of relevant monitoring experience (on-site and remote) Required
Proficient with MS Office Suite High
Excellent computer and organizational skills High
High level of attention to detail required High
Ability to work on varying projects and exercise critical thinking High
self starter who can work remotely and a team player who can work cross functionally with some oversight High
Knowledgeable in clinical research operations, including interpretation and implementation of country regulations and ICH guidelines, as required per their role as a CRA High
Excellent organizational, interpersonal, and communication skills both oral and written High
Demonstrated problem solving skills, self motivated, and adaptable to a dynamic environment High
Knowledgeable in prioritization, problem solving, organization, critical thinking, decisionmaking, time management, and planning activities High
Ability to collaborate with internal and external colleagues and work well in a team oriented setting High

If you’re looking for a career where your work advances global health and where scientific excellence meets real-world impact, join us and be part of something bigger. One Team, One Purpose.

CONNECT WITH US!
Find us on LinkedIn:/the-emmes-group/
Visit our website:https://www.theemmesgroup.com/

Apply Now

Refine Your Search

Research Associate jobs in Silver Spring, MD

Clinical Research Associate II

Research Associate I - MRBD

Research Associate

Research Assistant/Associate - Junior Evaluator

In-House Clinical Research Associate

Clinical Research Associate

Research Associate II - Preventive Medicine & Biostatistics

Research Assistant- Rockville

In-House Clinical Research Associate

Research Associate II

Research Associate I - Public Health Research - DC Hybrid Office

Research Associate

Research Associate

Senior Research Associate

Senior Clean Energy Research Associate

Sr. Clinical Research Associate

Associate Research Scientist

Clinical Research Assistant I - MED

Research Associate

Research Project Associate

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