182 Results for

Clinical Research Coordinator Jobs in Maryland

Jobs

New!

Germantown, MD5 days ago

$120,000–$140,000 Per Year

Information collected and processed as part of your Jobot candidate profile, and any job applications, resumes, or other information you choose to submit is subject to Jobot's Privacy Policy, as well as the Jobot California Worker Privacy Notice and Jobot Notice Regarding Automated Employment Decision Tools which are available at jobot.com/legal. Conducts site visits including but not limited to Pre-study visits, initiation visits, interim monitoring visits, close-out visits to ensure compliance with protocols, Sponsor SOPs, ICH/GCP and all applicable regulations.

Elkridge, MD7 days ago

$22.48–$39.75

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.

New!

Bethesda, MD6 days ago

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).

Annapolis, Maryland30+ days ago

$51,545–$88,987 Per Year

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. Duties include but not limited to assuring protocol compliance for all patients enrolled in the trial, participation in the informed consent process, perform ongoing assessments and documentation in collaboration with physicians and other providers.

Frederick, Maryland30+ days ago

$58,798–$77,435 Per Year

Silver Spring, MD13 days ago

$27.75–$44 Per 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.

Bethesda, Maryland30+ days ago

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.

Baltimore, MD30+ days ago

$45,000–$100,000 Per Year

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.

Bethesda, MD30+ days ago

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.

New!

Bethesda, MD6 days ago

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.

Silver Spring, Maryland7 days ago

$58,798–$77,435 Per Year

Prepares study‑related documentation, including protocol worksheets, adverse event reports, institutional review board (IRB) documents, and annual continuing review reports. Ensures research quality by adhering to organizational SOPs, principles of Good Clinical Practice (GCP), and applicable federal, state, and local regulations, including OSHA, CDC, and HIPAA.

New!

Baltimore, MDToday

$60–$64 Per Hour

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. Work products and documents related to data entry in the electronic medical record system., generating reports; perform study procedures; process and destroy specimens as needed; maintain storage records/inventory of biological specimens.

Baltimore, MD30+ days ago

$100,000–$113,000 Per 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.

Bethesda, MD20 days ago

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.

Bethesda, MD27 days ago

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.

New!

Bethesda, MDToday

$55,000–$60,000 Per Year

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.

Bethesda, Maryland30+ days ago

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.

New!

Silver Spring, MD6 days ago

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Baltimore, Maryland7 days ago

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.

New!

Laurel, MD6 days ago

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.

Baltimore, MD30+ days ago

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.

Silver Spring, MD20 days ago

REQUIRED DEGREE/EDUCATION/CERTIFICATION: Required to be a Registered Nurse licensed to practice in the state of Maryland, who are skilled and qualified in nursing procedures to include, but not limited to phlebotomy and the administration of experimental vaccines and other parenteral therapeutics as per specific protocol guidance in accordance with the 21 Code of Federal Regulation (CFR) 11, 50, 54, 56, 312, and 314. The Family of Companies (FOCs) includes Keaki Technologies, Laulima Government Solutions, Kpono Government Services, and Kapili Services, Pookela Solutions, Kkaha Solutions, LLC, and Pololei Solutions, LLC.

Gaithersburg, MD30+ days ago

$26.90–$34.35 Per Hour
Part-time

Recently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Responsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.

New!

Rockville, MD6 days ago

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.

New!

Gaithersburg, Maryland3 days ago

Silver Spring, MD13 days ago

Build financial console in OnCore CTMS including protocol amendments and updates to ensure accurate charge capture and segregation of research charges for all research related patient care as well as ancillary services such as investigational pharmacy. 3 years experience working in a clinical research environment including a stand-alone research site, a research department, or in research administration such as a centralized research office, or with an institutional review board (Required).

New!

Rockville6 days ago

Possesses basic knowledge of the study protocol, site monitoring plan, and study manuals to triage questions or requests from site staff e.g., enrollment updates, questions, missing documentation, meeting arrangements, etc. 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.

New!

Rockville3 days ago

Baltimore, MD30+ days ago

4. 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. Position Objective: The Community Brain Health Study Research Coordinator will independently provide support services to satisfy the operational objectives of the Brain Health Equity (BHE) Unit within the Health Disparities Research Section (HDRS) at the National Institute on Aging (NIA).

Bowie, MD30+ days ago

Logs/completes information on sponsor systems and ensures all information provided is accurate (i.e., case report forms, EDC, etc.) and ensures it is completed within timeframe. " Performs all defined study activities (i.e., informed consent, screening, and protocol procedures which include but not limited to vital signs, pregnancy tests, height, weight, ECG's, etc.).

Olney, MD30+ days ago

$102,606–$196,996 Per Year

Consistently demonstrates support for compliance in the performance of job duties and responsibilities by a) developing and maintaining knowledge of and performing job functions in compliance with rules regulations policies and statutes that affect his/her job; b) maintaining knowledge of and performing job functions in compliance with MedStar Health and MedStar Health Research Institute policies and procedures; and c) reporting compliance concerns in an appropriate and timely manner. Ensure the safety and welfare of study subjects to include symptom review and management appropriate referral and follow-up and ongoing contact with subjects and primary care providers regarding current health status and response to study interventions.

Baltimore, Maryland7 days ago

Requirements: Bachelor's degree OR 2 years of college in a health-related program OR completion of a medical assistant, phlebotomist, or other healthcare-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP required. As a Clinical Research Assistant, you’ll play a key role in supporting study visits, interacting with patients, and ensuring research is conducted safely and accurately.

New!

Baltimore, Maryland6 days ago

2. 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. Extensive experience in conducting community outreach and managing community relationships, especially in historically marginalized communities, such as Black communities in urban settings.

Olney, MD30+ days ago

$102,606–$196,996 Per Year

Olney, Maryland30+ days ago

$102,606–$196,996 Per Year

Baltimore, MD30+ days ago

This general interest posting is designed for Clinical Research Assistants (RAs) 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. We welcome interest from candidates who bring: A bachelor's or master's degree involving 1+ year of laboratory classes, preferably within a scientific or healthcare-related field (e.g., biology, chemistry, psychology, pre-med, or similar) and/or.

Silver Spring, MD30+ days ago

Critical thinking skills ability to analyze clinical research protocols, assess study budgets, and analyze clinical trial contracts including payment terms. Excellent communication skills, ability to interact across the organization, and negotiate with clinical research sponsor/ clinical research organization personnel in a professional manner to represent CNH.

Baltimore, MD27 days ago

$63,000–$74,000 Per Year

Provides training to less experienced researchers; assisting in developing and submitting grants, papers, abstracts, manuscripts, and presenting studies; developing protocol manuals and data collection instruments; participating in field visits, responding to requests and questions from individuals, institutions, government agencies, and funding agencies; and participating in the design of research studies. Exempt regular staff receive a generous PAID leave package that includes over 4 weeks of vacation accrued each year, 15 paid holidays, 3 personal leave, unlimited accrual of sick time, and comprehensive health insurance; professional learning and development programs; tuition remission for employees and their dependents at any University System of Maryland school; and flexible work schedules and teleworking options (if applicable per job).

Baltimore, MD30+ days ago

$57,000–$63,000 Per Year

Contingent Category II staff receive a generous leave package that includes over 2 weeks of vacation each year, paid holidays, sick time, and time for community service; subsidized comprehensive health insurance and supplemental retirement options; professional learning and development programs; limited tuition remission for employees enrolled at UMB; life insurance and long-term disability; and flexible work schedules and teleworking options (if applicable per job). The University of Maryland, Baltimore (UMB) School of Medicine, Department of Trauma Research Advanced Resuscitation in Combat Casualty Care Laboratory (ARC3 Lab), is seeking a full time Sr Research Project Coordinator to provide advanced support for research administration, data and account management, and laboratory logistics.

Bethesda, MD30 days ago

$50,000–$80,000 Per Year

Keywords: Clinical Research, Clinical Trials, Clinical Operations, In-House CRA, TMF, Trial Master File, eTMF, Veeva Vault, Regulatory Documents, Regulatory Affairs, Document Management, ICH GCP, FDA Regulations, Good Clinical Practice, Essential Documents, Site Document Collection, IRB Submissions, OHRP Regulations, Site Start-Up, Study Coordination, Clinical Study Support, Monitoring Support, TMF Maintenance, Document Tracking, Compliance, Audit Readiness, Clinical Data Management, Sponsor Oversight, CRO, Protocol Compliance, Investigator Communication, Site Management, Clinical Systems, Database Tracking, Microsoft Excel, Microsoft Word, Microsoft Outlook. Responsibilities of the In-House Clinical Research Associate include: Review and process essential regulatory documents received from clinical trial sites.

Baltimore, MD20 days ago

$48,000–$51,000 Per Year

Exempt regular staff receive a generous PAID leave package that includes over 4 weeks of vacation accrued each year, 16 paid holidays, 3 personal leave, unlimited accrual of sick time, and comprehensive health insurance; professional learning and development programs; tuition remission for employees and their dependents at any University System of Maryland school; and flexible work schedules and teleworking options (if applicable per job). This position is within the Maryland Addiction Consultation Service team, working to support evaluation and continuous quality improvement as part of a team that provides statewide consultation, training and technical assistance to health care providers and teams in an effort to increase access to evidence based treatment for substance use disorders.

Baltimore, MD30+ days ago

$48,000–$53,000 Per Year

Contingent Category II staff receive a generous leave package that includes over 2 weeks of vacation each year, paid holidays, sick time, and time for community service; subsidized comprehensive health insurance and supplemental retirement options; professional learning and development programs; limited tuition remission for employees enrolled at UMB; life insurance and long-term disability; and flexible work schedules and teleworking options (if applicable per job). Lead the collection and management of study data by developing data collection instruments, establishing and maintaining databases, and performing data quality checks.

Bethesda, MD22 days ago

$50,000–$70,000 Per Year

Piper Companies is seeking a Clinical Research Associate (CRA) to support the operational delivery of clinical trials across infectious disease, oncology, and cardiology programs. Collaborate cross-functionally with CRAs, CTMs, QA, and Data Management teams to resolve issues, mitigate risks, and maintain compliance with ICH-GCP and SOPs.

Germantown, MD21 days ago

$58,000–$68,000 Per 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. We're proud of the impact we make and just last year, we supported over 780 discovery projects, 1,000+ CMC programs, and 1,000+ clinical trials across all phases.

Baltimore, MD30+ days ago

Mercy Medical Center is honored to be recognized by Newsweek as one of America's Most Trustworthy Companies for three consecutive years (20232025) and as one of America's Greatest Workplaces for Women in 2025. Position requires a working knowledge and experience with the following computer packages: Microsoft Office (including Word, Access, Excel, PowerPoint.

Baltimore, MD30+ days ago

Education and Work Experience: • Must possess a Bachelor's Degree • 2 years of experience preferred • Advanced knowledge of Microsoft Office Suite (Word, Excel, Access, PowerPoint) is a plus • Experience with clinical/patient interactions is a plus. Mercy Medical Center is honored to be recognized by Newsweek as one of Americas Most Trustworthy Companies for three consecutive years (2023-2025) and as one of Americas Greatest Workplaces for Women in 2025.

Bethesda, Maryland30+ days ago

The Research Coordinator provides assistance to the Principal Investigator and Study Team coordinating research activities that may include recruiting research participants, data collection and management and other research activities as assigned. 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 .

Germantown, MD30+ days ago

$65,000–$75,000 Per Year

As Clinical Research Associate (CRA) you will act as the primary contact for clinical study sites, ensuring smooth study start‑up, effective monitoring and high‑quality data collection in a regulated environment. Ensuring timely data collection and performing source data verification / Source Data Review, resolving data queries and supporting database verification and database lock.

Rockville30+ days ago

Remote

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. Responsibilities: 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.

Glen Burnie, MD30+ days ago

$41.50–$56.68 Per 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!

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Clinical Research Coordinator Jobs in Maryland

Sr. Oncology Clinical Research Associate Jobot

Pharmacy Technician Clinical Coordinator MedStar Health

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

Clinical Research Coordinator II - Annapolis/Columbia Maryland Oncology

Clinical Research Coordinator II (Frederick/Germantown) Maryland Oncology

Clinical Research Coordinator Trinity Health

Senior Clinical Research Coordinator The Geneva Foundation

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

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 II-White Oak Maryland Oncology

Temporary - Clinical Research Coordinator Axle

Clinical Research Nurse Coordinator Pharmaron Beijing Co Ltd

Clinical Research Coordinator III - Pediatrics 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 DelRicht Research

Clinical Research Coordinator The Geneva Foundation

Clinical Research Coordinator II-White Oak US Oncology Inc

Clinical Research Coordinator Headlands Research

Clinical Research Coordinator I - Bilingual (Spanish) ObjectiveHealth Inc

Clinical Research Coordinator Headlands Research Inc

Clinical Research Coordinator III Alakaina Foundation Family of Companies

Clinical Research Coordinator I CBH Health LLC

Clinical Research Coordinator Children's National Hospital

Clinical Research Coordinator I CenExel

Clinical Research Revenue Cycle Coordinator II Children's National Hospital

In-House Clinical Research Associate Emmes Group

In-House Clinical Research Associate- Government Emmes Group

Community Brain Health Study Research Coordinator (50862) Gap Solutions, Inc.

Clinical and Health - Clinical Research Coord II Mindlance

Clinical Research Nurse Practitioner (NP) or Physician Assistant (PA) Mutli-site Coverage MedStar Health Research Institute

Phlebotomist - Clinical Research Assistant Headlands Research

Community Brain Health Study Research Coordinator Axle

Clinical Research Nurse Practitioner (NP) or Physician Assistant (PA) Mutli-site Coverage MedStar Health

Clinical Research Nurse Practitioner (NP) or Physician Assistant (PA) Multi-site Coverage MedStar Health

Clinical Research Assistant Opportunities - Multiple Locations Nationwide Headlands Research Inc

Sr. Clinical Research Budget Analyst Children's National Hospital

Research Project Specialist (Clinical Research Specialist) University of Maryland School of Medicine

Coordinator, Research Project Sr University of Maryland School of Medicine

In-House Clinical Research Associate Zp Group Llc

Clinical Research Assistant University of Maryland School of Medicine

Coordinator, Research Project University of Maryland School of Medicine

Clinical Research Associate (Hybrid) Zp Group Llc

Project Coordinator I, Clinical Kitting Pharmaron Beijing Co Ltd

Gastroenterology Research Coordinator Mercy Medical Center Inc

GI Research Coordinator Mercy Medical Center Inc

Research Coordinator (EVERGREEN) The Geneva Foundation

Clinical Research Associate Qiagen NV

Clinical Research Associate II Emmes Group

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

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