643 Results for

Clinical Coordinator Jobs in Washington, DC

Jobs

Washington, DC

$42.82–$78.27

li style="font-family:'arial' , 'helvetica' , sans-serif;font-size:12pt">Evaluates and interprets clinical information from diagnostic equipment for invasive cardiac procedures including R/L coronary angiography PTA Atherectomy Peripheral Stent placement pacemaker insertion IABP indwelling catheter insertion Dobutamine Stress Echo Transesophageal Echo etc. for adult patients.

Assists with administering the daily operations of the Cardiovascular Services Labs including case completion and also assures that all rooms are prepared appropriately for clinical procedures and overseeing adjunct services.

10 days ago

Fairfax, VA

In collaboration with other members of the management team, the CNC directs, monitors, and evaluates nursing care in accordance with established policies/procedures, serves as a resource person for staff, and models a commitment to the organization’s vision/mission/values to support an unparalleled patient experience and clinical outcomes that contribute to overall departmental performance.

Additional options for dental and vision benefits, life and disability coverage, flexible spending accounts, supplemental health protection plans (accident, critical illness, hospital indemnity), auto and home insurance, identity theft protection, legal counseling, long-term care coverage, moving assistance, pet insurance and more.

4 days ago

Reston, VA

4 days ago

Washington, DC

$89,065–$162,801

li>CPR - Cardiac Pulmonary Resuscitation (includes BLS and NRP) for healthcare providers from either the American Heart Association (AHA) or American Red Cross within 90 Days required. The primary responsibilities of the position will be the following: assisting in communications with patients; triaging patients and patient issues symptom management and patient education regarding their disease process and treatment.

10 days ago

Reston, VA

4 days ago

Falls Church, VA

HCA Healthcare has been recognized as one of the World's Most Ethical Companies® by the Ethisphere Institute more than ten times.Â In recent years, HCA Healthcare spent an estimated $3.7 billion in cost for the delivery of charitable care, uninsured discounts, and other uncompensated expenses.

4 days ago

Baltimore, MD

$40.12–$62.19 / hour

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Support: A culture of collaboration with resources like unit-based practice councils and advanced clinical education support — improving both workflow efficiency and patient outcomes and allowing you to work at the top of your license.

12 days ago

Laurel, MD

li>Not easily distracted: You have the ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies.

ObjectiveHealth is a clinical research company that uses proprietary technology to:

Increase patient access to research trials within our communities,
Provide physicians with enhanced care options for current patients, and.

14 days ago

Mclean, VA

$55,000–$60,000 / year

p>Overall, the Clinical Research Coordinator is responsible for delivering an excellent patient experience while driving accurate, efficient study execution across our DC-area clinics, ensuring:

Patients have a positive, professional, and comfortable experience throughout their time in our clinic.
Preferred: Experience in a patient-facing or client-facing healthcare setting such as medical offices, pharmacies, dental offices, surgical settings, medical spas, or similar environments.

8 days ago

Washington

Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events; makes decisions as when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Coordinates the development of forms, questionnaires and the application of research techniques; assists in writing instructional procedure manuals for study progress, data collection and coding; reviews journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies.

30+ days ago

Silver Spring, MD

$27.75–$44 / hour

Holy Cross Hospital, in Silver Spring, is one of the largest hospitals in Maryland, and Holy Cross Germantown Hospital is the first hospital in the nation built on a community college campus, enhanced by an educational partnership. Position Purpose: The Clinical Research Coordinator coordinates pharmaceutical company, National Cancer Institute (NCI), multisite and in-house protocol activities for the Cancer Program and principal investigators.

21 days ago

Silver Spring, MD

$27.75–$44 / hour

Position Purpose:

The Clinical Research Coordinator coordinates pharmaceutical company, National Cancer Institute (NCI), multisite and in-house protocol activities for the Cancer Program and principal investigators.

3 days ago

Loudoun, Leesburg, VA

15 days ago

Baltimore, MD

$45,000–$100,000 / year

p>This general interest posting is designed for experienced Clinical Research Coordinators (CRCs) who may not see a current opening that aligns with their location, but want to be considered for future opportunities across our growing network of clinical research sites nationwide. They play a hands-on role in advancing new therapies, supporting patients through clinical trials, and ensuring studies are conducted with the highest level of quality and care.

30+ days ago

Bethesda, Maryland

li>Maintain and update files of all applicable regulatory documentation for IACUC or IRB (including protocols, approvals, amendments, modifications, etc.) as well as any communications with the sponsor or any other Federal or regulatory office (including prior approvals, change in scope, etc.

Coordinate the day-to-day activities of technical support staff specifically engaged in the carrying out of research/clinical protocol, as appropriate to the position; may perform aspects of research protocol, as required, in accordance with specified program objectives.

30+ days ago

Washington, DC, Washington, DC

This is an excellent opportunity for someone who enjoys building patient relationships, thrives in a fast-paced environment, and is passionate about helping patients begin their smile journey.

Our ideal candidate is confident presenting treatment plans, discussing financial arrangements, and creating an exceptional patient experience from the very first visit.

30 days ago

Bethesda, MD

li>Coordinates with therapy teams and study leadership to ensure protocol‑driven timing, data collection, and session requirements are met, particularly in support of MDMA‑assisted therapy sessions. This position will be critical in ensuring compliance, safety, and efficiency at all stages of the study lifecycle, including but not limited to study startup, participant recruitment efforts, data and specimen collection, project tracking, and study operations.

30+ days ago

Bethesda, MD

Within the Directorate is the NMRC Clinical Trials Center (CTC), a 3,500 square foot state-of-the-art facility located in Bethesda, MD that is equipped to conduct Phase 1 and 2 outpatient clinical trials.

Assists human subjects' research activities, to include clinical trial protocol development, study operational procedures and forms development, and study implementation within the NMRC CTC in conjunction with senior staff.

14 days ago

Rockville, MD

We are seeking applications from aspiring clinical researchers (and clinicians) who are committed to cutting-edge work using community-based, neurodiversity affirming, qualitative, and neuroimaging (EEG/ERP, fMRI) methods to improve quality of life for autistic people. Independently coordinates, conducts and documents visits and protocol-specific testing/interviews according to study protocol, operational plans of clinical departments and SOPs for minimal risk studies or for other studies under direction.

14 days ago

Silver Spring, Maryland

$58,798–$77,435 / year

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Job Description

Key Responsibilities.
Job Profile Summary

Responsible for recruiting, screening, consenting, and enrolling patient in clinical trials.
15 days ago

Washington, DC

CRC serves as a key liaison between investigators, sponsors, and multidisciplinary teams, while supporting data integrity, resolving operational challenges, and mentoring pool coordinators to ensure high-quality, efficient research operations. Accurately creates, completes, maintains, organizes and accounts for study materials, including participant lists and visit logs, regulatory binders, case report forms, laboratory kits, investigational product(s) and participation incentives.

16 days ago

Glen Burnie, MD

$41.50–$56.68 / hour

In addition, the Clinical Coordinator will continuously assess unit needs to ensure adequate resources for current and upcoming shifts by collaborating with the Nurse Manager, other departments clinical and nonclinical, to coordinate admissions, transfers, and discharges of patients.

Experience the highest level of appreciation at UM Baltimore Washington Medical Center - named Top Workplace in the Baltimore area by The Baltimore Sun two years in a row (2019 & 2020); Top Workplace in the USA for 2021!

30+ days ago

$47,586–$87,558.13 / year

must respond to questions from patients in their portfolio in a timely manner; triage issues as they arise,

facilitate communication between the PI/Sub-Is and patients for adverse events and clinical concerns,

schedule future visits, send reminders for upcoming visit, ensure that the timing of the visit will work for any.

2 days ago

Bethesda, MD

li>Axillary radiotherapy or axillary lymph node dissection in patients with clinically node-positive breast cancer undergoing upfront tailored axillary surgery: An international, randomized superiority trial (NOAX). Current research portfolio supported by this role includes data and biorepositories, associated utilization studies, cfDNA and CTC in breast cancer, and clinical trials (drug, device, surgical intervention).

14 days ago

Bethesda, MD

This Phase I study conducted at the Uniformed Services University Translational Medicine Unit, is a randomized, placebo-controlled, double-blind, 4-period crossover study comparing LT-120, an intranasal esketamine nasal spray, with intravenous racemic ketamine under fasted conditions. We serve military, medical, academic and government clients by administering, managing and supporting preeminent scientific programs that benefit members of the armed forces and civilians alike.

30+ days ago

$21.16–$35.29 / hour

With the Hilltop Campus located in the heart of the historic Georgetown neighborhood, and the Capitol Campus, just minutes from the U.S. Capitol and U.S. Supreme Court, Georgetown University offers rigorous academic programs, a global perspective, and unparalleled opportunities to engage with Washington, D.C. Our community is a close-knit group of remarkable individuals driven by intellectual inquiry, a commitment to social justice, and a shared dedication to making a difference in the world. The Clinical Research Coordinator II (CRC II) is a lead coordinator on multiple surgical services (General Surgery, Burn, Breast, Endocrine, Trauma, Colorectal, and Surgical Oncology) and possibly transplant clinical research studies, under the oversight of the Principal Investigator (PI) and direct supervision of the Clinical Research Nurse Manager in collaboration with a Research Director.

30+ days ago

Baltimore, Maryland

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Assist staff on all facets of clinical studies including subject enrollment, scheduling outpatient appointments and inpatient admissions, travel arrangements, investigation consent, subject longitudinal monitoring, study data, sample collection and data entry.

Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad.

4 days ago

Glen Burnie, MD

$41.50–$56.31 / hour

30+ days ago

Fairfax, VA

Full time

PFS benefits, compensation, and bonuses are determined by various factors, including but not limited to location, the individual's particular combination of education, knowledge, skills, competencies, and experience, as well as contract and organizational requirements. Essential Duties and ResponsibilitiesCoordinate day-to-day clinical research activities, including regulatory submissions, patient screening enrollment, and data management.

22 days ago

Bowie, MD

$33–$38

Flourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources.

4 days ago

Bethesda, MD

Serves as the clinical and operational lead for assigned studies, leveraging clinical research expertise to guide and oversee protocol-specific clinical procedures, including participant assessments, specimen collection (e.g., pediatric blood draws), and administration of study interventions such as vaccines. Rare after-hours phone availability may be required to serve as a point of contact for emergency participant needs and to coordinate with the Principal Investigator and other study team members regarding serious adverse event (SAE) assessment and reporting, or any other urgent participant-related matters.

28 days ago

Fairfax, Virginia

CMI faculty have active collaborations with healthcare institutions including the Walter Reed National Military Medical Center, INOVA, Children's National Medical Center, National Rehabilitation Hospital, government agencies such as the FDA, as well as federal laboratories such as the Naval Research Laboratory, NIH Clinical Center, and a number of academic medical centers in the National Capital Region. Contribute to research with high public health significance, including chronic pain and disability; Work closely with researchers using cutting edge technology, such as ecological momentary assessment, biomechanical assessments, AI and natural language processing, 3D motion capture, and advanced medical imaging; and.

30+ days ago

Baltimore, MD

$100–$113 / year

Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. This role requires a licensed Registered Nurse with proven clinical experience, preferably in a research setting, who is capable of working independently and collaboratively to ensure the safety, well-being, and informed consent of all research participants.

17 days ago

Washington

or call the dedicated accommodation inquiry number at 314-935-1149 and leave a voicemail with the nature of your request.

All qualified individuals must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship.

Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; identifies problems and/or inconsistencies and monitors participant’s progress to include documentation and reporting of adverse events; resolves IRB/protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.

23 days ago

Washington

Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.

30+ days ago

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Knowledge of health care field; medical practice clinical and administrative systems, departments, and practices, including clinical financial policies and reimbursement payment requirements. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions:

Physical demands: Involves sitting approximately 90 percent of the day, walking or standing for the remainder.

30+ days ago

Baltimore, Maryland

div>

Headlands Research will never ask a candidate for personal identifiable information (date of birth, social security number, driver’s license information, etc) via email or messenger tools, or for a financial deposit of any kind.

15 days ago

Falls Church, VA
$25–$35 / hour
The work environment is fast paced and requires consistent attention to detail, particularly when performing chart reviews, working in the EMR, and entering data into EDC systems. If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.
29 days ago

Annapolis, Maryland
$51,545–$88,987 / year
Responsibilities:
Job Description
Key Responsibilities.
In collaboration with the physician, reviews patients for changes in condition, adverse events, concomitant medication use, protocol compliance, response to study drug and thoroughly documents all findings and participates in data collection of all subjects.
30+ days ago

Baltimore, MD
p>Requirements:
Bachelor's degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required OR licensed as a Licensed Practical Nurse (LPN) or higher. As a leading network of advanced clinical trial sites, we leverage cutting-edge technology and exceptional support services to broaden outreach and participation.
30+ days ago

Elkridge, MD
$22.48–$39.75 / hour
p>Key responsibilities include supporting various aspects of clinical operations, such as benefits investigation, prior authorization, copay and financial assistance coordination, new patient onboarding, medication delivery coordination, drug replacement services, and conducting outbound calls to support prescription refills.
Proactively tracks patient refills coming due, proposes orders to providers, escalates clinical issues to a pharmacist as required, and performs outreach to patients to ensure coordination of all aspects of medication management.
30+ days ago

Washington
div>

Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.
Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.

30+ days ago

Washington
Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events; makes decisions as to when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Recruits and enrolls study participants; makes and/or participates in making determinations of eligibility based on diagnostic criteria and/or observations/analysis in participant interviews; develops informed consent packets for study participants and confers with participants to explain purpose of study and obtain completed informed consent packets; explains diagnostic procedures and treatment plans to address participant/family concerns; administers/scores tests and/or evaluates all lab and clinical assessments to ensure they are completed in a timely manner.
30+ days ago

Washington
div>

Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events; makes decisions as when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency.
Coordinates the development of forms, questionnaires and the application of research techniques; assists in writing instructional procedure manuals for study progress, data collection and coding; reviews journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies.

30+ days ago

Washington
Implements and manages all phases of study/protocol; ensures compliance with protocol guidelines and requirements of regulatory agencies; establishes record-keeping systems; makes assessments and determinations of participants’ progress in the study; analyzes, investigates and reports adverse events; makes decisions as when to notify physicians of issues, when to stop participant inclusion and/or to make and/or recommend adjustment of the protocol of particular participants; resolves protocol management issues and recommends corrective action as appropriate; serves as liaison with funding or sponsoring agency. Coordinates the development of forms, questionnaires and the application of research techniques; assists in writing instructional procedure manuals for study progress, data collection and coding; reviews journals, abstracts and scientific literature to keep abreast of new developments and to obtain information regarding previous studies to aid in the planning of new studies.
30+ days ago

Baltimore, MD
$60–$64 / hour
li>
Assist staff on all facets of clinical studies including subject enrollment, scheduling outpatient appointments and inpatient admissions, travel arrangements, investigation consent, subject longitudinal monitoring, study data, sample collection and data entry.
Axle is a bioscience and information technology company that offers advancements in translational research, biomedical informatics, and data science applications to research centers and healthcare organizations nationally and abroad.
8 days ago

Silver Spring, MD
p>Cookies are used on this site to assist in continually improving the candidate experience and all the interaction data we store of our visitors is anonymous.
We're sorry, but it looks like this job may be no longer available or does not exist.
14 days ago

New
Calverton, MD
p>Cookies are used on this site to assist in continually improving the candidate experience and all the interaction data we store of our visitors is anonymous.
We're sorry, but it looks like this job may be no longer available or does not exist.
3 days ago

Washington
ul>
Acts as primary liaison to Principal Investigator (PI) to develop plans for investigator-initiated research projects; prepares budgets and assists in preparing grant proposals to sponsoring agencies; writes or assists in writing initial study protocol and instructional manuals; preparation of amendments to protocols and/or modification to study design, as appropriate. or call the dedicated accommodation inquiry number at 314-935-1149 and leave a voicemail with the nature of your request.
All qualified individuals must be able to perform the essential functions of the position satisfactorily and, if requested, reasonable accommodations will be made to enable employees with disabilities to perform the essential functions of their job, absent undue hardship.
30+ days ago

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Clinical Coordinator Jobs in Washington, DC

Clinical Nurse Coordinator (RN) Cardiovascular Services - Relocation Offered! MedStar Health

Nurse Clinical Coordinator Emergency Dept StoneSprings Hospital Center

RN Clinical Coordinator Medical Unit Reston Hospital Center

Clinical Nurse Coordinator (RN) Medical Oncology - Relocation Offered! MedStar Health

Clinical Nurse Coordinator Medical Unit Reston Hospital Center

Mental Health Clinical Nurse Coordinator RN Dominion Hospital

Care Coordinator RN LifeBridge Health

Clinical Research Coordinator I - Bilingual (Spanish) ObjectiveHealth Inc

Clinical Research Coordinator DelRicht Research

Clinical Research Coordinator I (Data) - Medical Oncology Washington University in St Louis

Clinical Research Coordinator Trinity Health

Clinical Research Coordinator (PRN Days) Trinity Health

Clinical Research Coordinator Virginia Heart

Clinical Research Coordinator I/II/III Opportunities - Multiple Locations Nationwide Headlands Research Inc

Senior Clinical Research Coordinator The Geneva Foundation

Treatment Coordinator Smile Horizon Orthodontics

Clinical Research Coordinator II - MDMA-AT The Henry M Jackson Foundation for the Advancement of Military Medicine Inc

Clinical Research Coordinator II - TraCR The Henry M Jackson Foundation for the Advancement of Military Medicine Inc

Clinical Research Coordinator Children's National Hospital

Clinical Research Coordinator II-White Oak Maryland Oncology

Key Responsibilities. Job Profile Summary Responsible for recruiting, screening, consenting, and enrolling patient in clinical trials.Apply15 days ago

Sr. Clinical Research Coordinator Children's National Hospital

Clinical Coordinator (RN), MedSurg University of Maryland Baltimore Washington Medical Center

Clinical Research Coordinator I Georgetown University

Clinical Research Coordinator II - MCCRP The Henry M Jackson Foundation for the Advancement of Military Medicine Inc

Clinical Research Coordinator I - SPA The Henry M Jackson Foundation for the Advancement of Military Medicine Inc

Clinical Research Coordinator II Georgetown University

Temporary - Clinical Research Coordinator (ID: 2026-2380) Axle

Clinical Coordinator (RN), Progressive Care Unit University of Maryland Baltimore Washington Medical Center

Clinical Research Coordinator Prometheus Federal Services

Clinical Research Coordinator Flourish Research

Clinical Research Coordinator III - Pediatrics The Henry M Jackson Foundation for the Advancement of Military Medicine Inc

Clinical Research Coordinator George Mason University

Clinical Research Nurse Coordinator Pharmaron Beijing Co Ltd

Clinical Research Coordinator III - Neurology Washington University in St Louis

Clinical Research Coordinator I - Neurology Washington University in St Louis

Clinical Research Coordinator - Urology (31159) GI Alliance

Clinical Research Coordinator Headlands Research

Clinical Research Coordinator Actalent Inc

Clinical Research Coordinator II - Annapolis/Columbia Maryland Oncology

Clinical Research Coordinator Headlands Research Inc

Pharmacy Technician Clinical Coordinator MedStar Health Research Institute

Clinical Research Coordinator I (Hybrid) - Neurology Washington University in St Louis

Clinical Research Coordinator I - Obstetrics and Gynecology Washington University in St Louis

Clinical Research Coordinator II - Neurology Washington University in St Louis

Clinical Research Coordinator II - Neurosurgery Washington University in St Louis

Temporary - Clinical Research Coordinator Axle

Clinical Research Coordinator II-White Oak US Oncology Inc

Clinical Research Coordinator (CRC) US Oncology Inc

Clinical Research Coordinator IV - Cardiology Washington University in St Louis

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Stand out to leading employers.

Key Responsibilities.
Job Profile Summary

Responsible for recruiting, screening, consenting, and enrolling patient in clinical trials.
15 days ago