Top 16 Research associate i Jobs in Maryland

Clinical Research Associate I
Emmes Group —Rockville, MD
- Full-time
- Bachelor's degree
- Organizational skills
- Experience equivalent to degree accepted
- Health insurance
- 401(k)
1h
Research Associate I/Microbiology and Molecular Genetics
Odyssey Consulting —Silver Spring, MD
- $60,000 - $62,000 a year
- Full-time
- Hybrid work
- Bachelor of Science
- Maintenance
- Analysis skills
- Health savings account
- Paid holidays
Research Associate I
Goldbelt, Inc. —Silver Spring, MD
- $57,000 - $63,000 a year
- Full-time
- Writing skills
- Maintenance
- Windows
- Health insurance
- Dental insurance
5d
Research Associate I/Microbiology and Molecular Genetics
Odyssey Systems Consulting Group, Ltd. —Silver Spring, MD
- $60,000 - $62,000 a year
- Full-time
- Hybrid work
- Bachelor of Science
- Maintenance
- Analysis skills
- Health savings account
- Paid holidays
Research Associate I, Tissue Engineering
Frederick National Laboratory —Frederick, MD
- $58,200 - $83,353 a year
- Full-time
- Bachelor's degree
- Fair chance
- Experience equivalent to degree accepted
Research Associate I - Influenza Immunology (VICD)
Frederick National Laboratory —Frederick, MD
- $58,200 - $83,353 a year
- Full-time
- Master's degree
- Databases
- Bachelor's degree
Research Assistant I - Pharmacology
Henry M. Jackson Foundation —Bethesda, MD
- $19.33 - $25.00 an hour
- Full-time
- Entry level
- Health insurance
- Dental insurance
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
Research Associate (I, II, III) - Uniformed Services University
The Geneva Foundation —Rockville, MD
- $50,000 - $63,000 a year
- Full-time
- In person
- Computer literacy
- Mid-level
- University
Quick Apply
Research Assistant I - PHA-AFRRI
Henry M. Jackson Foundation —Bethesda, MD
- $19.33 - $24.00 an hour
- Full-time
- Entry level
- Health insurance
- Dental insurance
Research Assistant I - MIC
Henry M. Jackson Foundation —Bethesda, MD
- $19.33 - $21.00 an hour
- Full-time
- Entry level
- Health insurance
- Dental insurance
Research Assistant I (Temporary, Part-Time) - CPDR
Henry M. Jackson Foundation —Bethesda, MD
- $19.33 - $22.50 an hour
- Part-time
- Office
- Entry level
7d
Research Assistant I - OUMD
Henry M. Jackson Foundation —Silver Spring, MD
- $19.33 - $25.00 an hour
- Full-time
- Entry level
- Health insurance
- Dental insurance
Research Assistant I - Animal Model Research
Henry M. Jackson Foundation —Bethesda, MD
- $19.33 - $24.00 an hour
- Full-time
- Entry level
- Health insurance
- Dental insurance
Research Technician I, Necropsy
Champions Oncology Inc. —Rockville, MD
- $22 - $24 an hour
- Weekends as needed
- Computer literacy
- Bachelor of Science
- Ability to lift 50 pounds
14d
Associate Scientist I – Bacterial Mutation
BASI GAITHERSBURG LLC —Rockville, MD
- From $60,600 a year
- Full-time
- Computer skills
- 1 year
- Associate's degree
- Paid parental leave
- Disability insurance
Quick Apply
8d

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Research Associate I/Microbiology and Molecular Genetics
Odyssey Consulting —Silver Spring, MD
We streamline defense acquisition and sustainment, engineering the technical battlefield with domain-specific proficiency to ensure lethality.
$60,000 - $62,000 a year
Research Associate I/Microbiology and Molecular Genetics
Odyssey Systems Consulting Group, Ltd. —Silver Spring, MD
We streamline defense acquisition and sustainment, engineering the technical battlefield with domain-specific proficiency to ensure lethality.
$60,000 - $62,000 a year

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Clinical Research Associate I

Emmes Group -
Rockville, MD

Apply Now

Job Details

Full-time
1 hour ago

Benefits

Health insurance
401(k)
Tuition reimbursement
Work from home
Parental leave

Qualifications

Project reporting
Data quality checks
Clinical study protocols and reports
Informed consent
Adverse event reporting
Operations coordination
Regulatory compliance
ICH guidelines
Clinical staff training
Bachelor's degree
Task prioritization
Clinical training
Scientific protocols
Team training
Organizational skills
Clinical trial standard operating procedures
Clinical trial patient safety management
Document archiving
Patient recruitment
Document quality checks
Productivity software
Clinical quality assurance standards
IRB compliance
1 year
Clinical trial site selection
Cross-functional collaboration
Clinical consent forms
Ethical review application preparation
Standard operating procedures (SOPs)
Communication skills

Full Job Description

Overview:

Clinical Research Associate I

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) I is responsible for monitoring clinical study sites either on-site 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 the supervision of the project CRA staff oversight lead, example, Clinical Study Manager, Lead CRA, Project Manager, etc., 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, 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 direction from the project CRA staff oversight lead.
Documents observations and monitoring activities in a site visit report at the conclusion of the visit with assistance and oversight by the project CRA staff oversight lead.
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 study related 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 sitespecific 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.
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 year of professional experience preferred Required
less than 1 year Prior clinical research experience (as a CTA, in-house CRA, CRC etc.) preferred Preferred
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 independently and a team player who can work cross functionally with heavy oversight High
Knowledgeable in clinical research operations, including interpretation and implementation of country regulations and ICH guidelines, as required 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.

Why work at Emmes?

At Emmes, your actions and hard work will have a direct impact on public health initiatives, both globally and in our local communities with opportunities for volunteerism through our Emmes Cares community engagement program. We offer a competitive benefits package focused on the health and needs of our growing workforce, including:

Flexible Approved Time Off

Tuition Reimbursement

401k Retirement Plan

Work From Home Anywhere in the US

Maternal/Paternal Leave

Casual Dress Code & Work Environment

CONNECT WITH US!

Follow us on Twitter - @EmmesCRO

Find us on LinkedIn - Emmes

The Emmes Company, LLC is an equal opportunity affirmative action employer and does not discriminate in its selection and employment practices. All qualified applicants will receive consideration for employment without regard to disability, protected veteran status, or other legally protected characteristics.

#LI-Remote

Apply Now

Refine Your Search

research associate i jobs in maryland

Clinical Research Associate I

Research Associate I/Microbiology and Molecular Genetics

Research Associate I

Research Associate I/Microbiology and Molecular Genetics

Research Associate I, Tissue Engineering

Research Associate I - Influenza Immunology (VICD)

Research Assistant I - Pharmacology

Research Associate I - MRBD

Research Associate (I, II, III) - Uniformed Services University

Research Assistant I - PHA-AFRRI

Research Assistant I - MIC

Research Assistant I (Temporary, Part-Time) - CPDR

Research Assistant I - OUMD

Research Assistant I - Animal Model Research

Research Technician I, Necropsy

Associate Scientist I – Bacterial Mutation

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