Top 2416 Clinical associate Jobs in Maryland

Clinical Research Associate II
Emmes Group —Rockville, MD
- Full-time
- Remote
- Mid-level
- Bachelor's degree
- Travel
- Health insurance
- 401(k)
In-House Clinical Research Associate
TECHNICAL RESOURCES INT'L —Bethesda, MD
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Writing skills
Research Associate II - MCCRP
Henry M. Jackson Foundation —Bethesda, MD
- $61,000 - $85,000 a year
- Part-time
- Remote
- Mid-level
- Health insurance
- Dental insurance
13d
Research Assistant/Associate - Junior Evaluator
MayaTech Corporation —Silver Spring, MD
- Full-time
- Master's degree
- Analysis skills
- Bachelor's degree
- Health 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
Clinical Research Coordinator I - MPS
Henry M. Jackson Foundation —Bethesda, MD
- $52,800 - $65,000 a year
- Full-time
- Remote
- Editing
- Entry level
- Health insurance
- Dental insurance
Assistant Clinical Analyst I (US)
GeneDx —Gaithersburg, MD
- $90,000 - $103,000 a year
- Medicine
- Computer literacy
- Analysis skills
13d
Clinical Trials Associate
TECHNICAL RESOURCES INT'L —Bethesda, MD
- Full-time
- Writing skills
- Mid-level
- Medical terminology
23h
Clinical Research Associate
VENESCO, LLC —Fort Detrick, MD
- $100,000 - $110,000 a year
- Nursing
- Mid-level
- 3 years
Quick Apply
Clinical Research Coordinator I - Medicine
Henry M. Jackson Foundation —Bethesda, MD
- Full-time
- University
- Entry level
- Health insurance
- Dental insurance
Associate Research Scientist, Real World Evidence
Precision AQ —Bethesda, MD
- $66,000 - $94,000 a year
- Online Application
- Remote
- Master's degree
- Organizational skills
- Communication skills
Quick Apply
2d
Clinical Information Specialist
TECHNICAL RESOURCES INT'L —Bethesda, MD
- Full-time
- Computer literacy
- Office
- Databases
Clinical Quality Management Specialist
Technical Resources International, Inc. —Bethesda, MD
- $65,000 - $85,000 a year
- Full-time
- Bachelor of Science
- Mid-level
- Quality control
1d
Clinical Informaticist - Ambulatory - Southern Maryland
MedStar Health —Waldorf, MD
- $82,617 - $157,352 a year
- Full-time
- Hospital
- Customer service
- Computer literacy
Clinical Research Coordinator
Concentric Methods —Bethesda, MD
- $30 an hour
- Full-time
- Mid-level
- Bachelor's degree
- 2 years
- Paid holidays
- Disability insurance
Clinical Trial Coordinator
Black Canyon Consulting —Bethesda, MD
- Mid-level
- Training & development
- Paid holidays
- Health insurance
Clinical Information Specialist
Technical Resources International, Inc. —Bethesda, MD
- $50,000 - $60,000 a year
- Full-time
- Hybrid work
- Computer literacy
- Office
- Databases
Medical Support Assistant - Federal Contract Position
Vision Quest Solutions Inc —Bethesda, MD
- Weekends as needed
- Background check
- Pass drug screening
- High school diploma or GED
Quick Apply
Research Associate II - Operational Knowledge Management
Henry M. Jackson Foundation —Bethesda, MD
- $61,000 - $80,000 a year
- Full-time
- Hybrid work
- Research
- Mid-level
- Project management
- 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

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Clinical Research Associate II

Emmes Group -
Rockville, MD

Apply Now

Job Details

Full-time

Benefits

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

Qualifications

Project reporting
Data quality checks
Clinical study protocols and reports
Clinical compliance checks
Informed consent
Adverse event reporting
Operations coordination
Regulatory compliance
Direct client contact
Routine inspections
Mid-level
Clinical audit and monitoring
ICH guidelines
Clinical staff training
Professional development support
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
Patient recruitment
Document quality checks
Clinical research inspection readiness
Productivity software
Clinical quality assurance standards

Full Job Description

Overview:

Clinical Research Associate II

US remotely and on-site (80% travel)

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.

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

clinical associate jobs in maryland

Clinical Research Associate II

In-House Clinical Research Associate

Research Associate II - MCCRP

Research Assistant/Associate - Junior Evaluator

Research Associate I - MRBD

Clinical Research Coordinator I - MPS

Assistant Clinical Analyst I (US)

Clinical Trials Associate

Clinical Research Associate

Clinical Research Coordinator I - Medicine

Associate Research Scientist, Real World Evidence

Clinical Information Specialist

Clinical Quality Management Specialist

Clinical Informaticist - Ambulatory - Southern Maryland

Clinical Research Coordinator

Clinical Trial Coordinator

Clinical Information Specialist

Medical Support Assistant - Federal Contract Position

Research Associate II - Operational Knowledge Management

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

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