Clinical Research Manager Jobs in Maryland
Clinical Research Manager jobs in Maryland are concentrated in pharmaceutical development, federal health research, and academic medical centers, with demand running from mid-level coordinators stepping into management through senior directors overseeing multi-site trials. The Baltimore-Columbia-Towson corridor, the Bethesda-Rockville biotech cluster, and the greater DC suburbs in Prince George's and Montgomery counties are the primary hiring hubs, where employers such as Johns Hopkins Medicine, the National Institutes of Health, and Covance anchor consistent openings. Protocol oversight, regulatory affairs, and oncology and infectious disease trial management are the most in-demand specialties across Maryland listings. Scan the live roles below and apply to whichever ones fit.
Find JobsOverview
Open roles65
Top employerJohns Hopkins University
Top cityBaltimore, MD
Cities hiring11
Work type57% Hybrid
Top industryEducation
Showing 5 of 65+ Clinical Research Manager jobs
Clinical Research Nurse (protocol development)
We won't show you this job again
Added 3d ago
Chenega Corporation
Clinical Research Nurse (protocol development)
Bethesda, Maryland
Added 3d ago
Clinical Research Assistant II
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Added 4d ago
Johns Hopkins University
Clinical Research Assistant II
Baltimore, Maryland
Added 4d ago
Sr. Clinical Research Associate
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Added 5d ago
The Emmes Company, LLC
Sr. Clinical Research Associate
Rockville, Maryland
Added 5d ago
Clinical Research Coordinator (SOM Pediatric Young Adult & Adolescent Medicine)
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Added 5d ago
Johns Hopkins University
Clinical Research Coordinator (SOM Pediatric Young Adult & Adolescent Medicine)
Baltimore, Maryland
Added 5d ago
Sr. Clinical Research Coordinator - Graduate School of Nursing
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Added 5d ago
The Henry M. Jackson Foundation for the Advancement of Military Medicine
Sr. Clinical Research Coordinator - Graduate School of Nursing
Bethesda, Maryland
Added 5d ago
Added 3d ago
Clinical Research Nurse (protocol development)
Chenega Corporation·Bethesda, Maryland
Job functions:
On-Site
5,001-10,000 employees
Job Description
Overview:
Our company offers employees the opportunity to join a team where there is a robust employee benefits program, management engagement, quality leadership, an atmosphere of teamwork, recognition for performance, and promotion opportunities. We actively strive to channel our highly engaged employee’s knowledge, critical thinking, innovative solutions for our clients.
Work Location: Onsite-9000 Rockville Pike, Bethesda, MD
Responsibilities:
Qualifications:
Minimum Qualifications: (To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.)
Knowledge, Skills and Abilities:
Physical Demands: (The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)
Chenega Services and Federal Solutions (CSFS) is seeking a Research Nurse to provide support services to the National Institutes of Health (NIH) Clinical Center.
Our company offers employees the opportunity to join a team where there is a robust employee benefits program, management engagement, quality leadership, an atmosphere of teamwork, recognition for performance, and promotion opportunities. We actively strive to channel our highly engaged employee’s knowledge, critical thinking, innovative solutions for our clients.
Work Location: Onsite-9000 Rockville Pike, Bethesda, MD
- Ensures human subjects protections and patient-orientation during the course of a research subject’s participation in clinical research protocol.
- Assists with protocol development, implementation, and management including overseeing the collection of concise and verifiable data that contributes to public health.
- Performs duties in the following areas: protocol compliance, contributing as a co-investigator on clinical trials as well as various collaborative projects, adherence to ethical standards, informed consent, patient recruitment and retention, management of clinical trials patients, documentation and document management, data management and information technology
- Assists in developing clinical research and protocol-specific standards of practice (SOP).
- Collaborates with the principal investigator to finalize, ensure implementation, assess efficacy, and revise corrective and preventive action plans.
- Participates in the preparation of reports for appropriate regulatory agencies and monitoring bodies or boards.
- Collaborates with PIs to resolve protocol implementation problems during design period; uses and revises/creates data capture forms to meet study needs.
- Collaborates with health care members in the execution and management of trials; communicates findings and suggestions to the PI based on expertise; reports clinical data to regulatory and monitoring agencies; produces reports for clinical use and treatment decision-making; and summarizes clinical data as requested by PIs.
- Develops supplemental materials for institutional review board (IRB) approval that assist in the informed consent process.
- Supports the informed consent process by continually providing patient/family counseling related to clinical trials and to the clinical trials process.
- Collaborates with PIs to revise eligibility criteria or change team processes according to protocol. Identifies problems in referral process and implements strategies to handle problems.
- Develops materials with input of PIs and IRB approval.
- Interviews and evaluates all patients being screened for entry into clinical trials.
- Develops study-specific materials for patient education and ensures IRB and sponsor approval, as required.
- Assesses for and addresses trends that affect patient adherence to protocol-specific activities.
- Interacts with physicians and web-based referral sources to assure that physicians and/or patients and their families receive answers to their questions and appropriate referral information in a timely manner.
- Collaborates with the interdisciplinary team to develop nursing practices that have the potential to improve patient outcomes.
- Assures timely scheduling of patients for appointments/testing and careful acquisition and distribution of clinical samples.
- Assures that all protocol required testing has been scheduled and patient visits are scheduled in accordance with protocol guidelines.
- Maintains involvement in all aspects of the clinical trial process.
- Conducts updates for patient care areas on protocol process and progress, and events impacting clinical care and data collection.
- Coordinates care for study participants. Care requirements are determined by the scope of the study participation and clinical conditions of the patient and the clinical effects on research procedures.
- Monitors the research participant for adverse events and reports to the study PI. Investigates the etiology of discrepancies or unusual sentinel events and provides feedback and recommendations for resolution and problem prevention.
- Participates in the development of approved source documents, templates, or forms.
- Participates in the preparation of reports for appropriate regulatory agencies and monitoring bodies or boards.
- Assists the principal investigator in developing data management plans for each clinical trial.
- Uses information management and computer technology to support clinical data management activities.
- Assists in developing case reporting forms (CRFs) for multisite clinical trials.
- Participates in and directs organizational audits performed by sponsor and/or regulatory agencies.
- Pursues opportunities to participate in local or national research-related activities (e.g., professional nursing and/or research organizations, institutional committees).
- Provides mentorship to new clinical trials nurses, research team members, and other healthcare providers.
- Performs other duties and responsibilities as assigned.
- Other duties as assigned
Qualifications:
Minimum Qualifications: (To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.)
- Minimum of an R.N. degree.
- Licensed as a nurse in any US State.
- Must be able to be credentialed by the NIH Clinical Center.
- Knowledge of environmental safety, including infection control, isolation technique, and general security.
- Knowledge pertaining to privacy of the patient, privileged information and secure handling of the patient’s medical records
- Knowledge of federal regulatory requirements pertaining to clinical research
- NIH clinical trials experience preferred
- Successfully pass background and drug screening
Knowledge, Skills and Abilities:
- Ability to read, write, and speak English well enough to effectively communicate with all parties.
- Computer literate.
Physical Demands: (The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)
- While performing the duties of this Job, the employee is regularly required to sit and talk or hear. The employee may use repeated motions that include the arms, wrists, hands and/or fingers. The employee is occasionally required to walk, stand, climb, balance, stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision.
Chenega Corporation
Clinical Research Nurse (protocol development)
Bethesda, Maryland
Added 3d ago5,001-10,000 employees
Job functions:
On-Site
Job Description
Overview:
Our company offers employees the opportunity to join a team where there is a robust employee benefits program, management engagement, quality leadership, an atmosphere of teamwork, recognition for performance, and promotion opportunities. We actively strive to channel our highly engaged employee’s knowledge, critical thinking, innovative solutions for our clients.
Work Location: Onsite-9000 Rockville Pike, Bethesda, MD
Responsibilities:
Qualifications:
Minimum Qualifications: (To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.)
Knowledge, Skills and Abilities:
Physical Demands: (The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)
Chenega Services and Federal Solutions (CSFS) is seeking a Research Nurse to provide support services to the National Institutes of Health (NIH) Clinical Center.
Our company offers employees the opportunity to join a team where there is a robust employee benefits program, management engagement, quality leadership, an atmosphere of teamwork, recognition for performance, and promotion opportunities. We actively strive to channel our highly engaged employee’s knowledge, critical thinking, innovative solutions for our clients.
Work Location: Onsite-9000 Rockville Pike, Bethesda, MD
- Ensures human subjects protections and patient-orientation during the course of a research subject’s participation in clinical research protocol.
- Assists with protocol development, implementation, and management including overseeing the collection of concise and verifiable data that contributes to public health.
- Performs duties in the following areas: protocol compliance, contributing as a co-investigator on clinical trials as well as various collaborative projects, adherence to ethical standards, informed consent, patient recruitment and retention, management of clinical trials patients, documentation and document management, data management and information technology
- Assists in developing clinical research and protocol-specific standards of practice (SOP).
- Collaborates with the principal investigator to finalize, ensure implementation, assess efficacy, and revise corrective and preventive action plans.
- Participates in the preparation of reports for appropriate regulatory agencies and monitoring bodies or boards.
- Collaborates with PIs to resolve protocol implementation problems during design period; uses and revises/creates data capture forms to meet study needs.
- Collaborates with health care members in the execution and management of trials; communicates findings and suggestions to the PI based on expertise; reports clinical data to regulatory and monitoring agencies; produces reports for clinical use and treatment decision-making; and summarizes clinical data as requested by PIs.
- Develops supplemental materials for institutional review board (IRB) approval that assist in the informed consent process.
- Supports the informed consent process by continually providing patient/family counseling related to clinical trials and to the clinical trials process.
- Collaborates with PIs to revise eligibility criteria or change team processes according to protocol. Identifies problems in referral process and implements strategies to handle problems.
- Develops materials with input of PIs and IRB approval.
- Interviews and evaluates all patients being screened for entry into clinical trials.
- Develops study-specific materials for patient education and ensures IRB and sponsor approval, as required.
- Assesses for and addresses trends that affect patient adherence to protocol-specific activities.
- Interacts with physicians and web-based referral sources to assure that physicians and/or patients and their families receive answers to their questions and appropriate referral information in a timely manner.
- Collaborates with the interdisciplinary team to develop nursing practices that have the potential to improve patient outcomes.
- Assures timely scheduling of patients for appointments/testing and careful acquisition and distribution of clinical samples.
- Assures that all protocol required testing has been scheduled and patient visits are scheduled in accordance with protocol guidelines.
- Maintains involvement in all aspects of the clinical trial process.
- Conducts updates for patient care areas on protocol process and progress, and events impacting clinical care and data collection.
- Coordinates care for study participants. Care requirements are determined by the scope of the study participation and clinical conditions of the patient and the clinical effects on research procedures.
- Monitors the research participant for adverse events and reports to the study PI. Investigates the etiology of discrepancies or unusual sentinel events and provides feedback and recommendations for resolution and problem prevention.
- Participates in the development of approved source documents, templates, or forms.
- Participates in the preparation of reports for appropriate regulatory agencies and monitoring bodies or boards.
- Assists the principal investigator in developing data management plans for each clinical trial.
- Uses information management and computer technology to support clinical data management activities.
- Assists in developing case reporting forms (CRFs) for multisite clinical trials.
- Participates in and directs organizational audits performed by sponsor and/or regulatory agencies.
- Pursues opportunities to participate in local or national research-related activities (e.g., professional nursing and/or research organizations, institutional committees).
- Provides mentorship to new clinical trials nurses, research team members, and other healthcare providers.
- Performs other duties and responsibilities as assigned.
- Other duties as assigned
Qualifications:
Minimum Qualifications: (To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.)
- Minimum of an R.N. degree.
- Licensed as a nurse in any US State.
- Must be able to be credentialed by the NIH Clinical Center.
- Knowledge of environmental safety, including infection control, isolation technique, and general security.
- Knowledge pertaining to privacy of the patient, privileged information and secure handling of the patient’s medical records
- Knowledge of federal regulatory requirements pertaining to clinical research
- NIH clinical trials experience preferred
- Successfully pass background and drug screening
Knowledge, Skills and Abilities:
- Ability to read, write, and speak English well enough to effectively communicate with all parties.
- Computer literate.
Physical Demands: (The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.)
- While performing the duties of this Job, the employee is regularly required to sit and talk or hear. The employee may use repeated motions that include the arms, wrists, hands and/or fingers. The employee is occasionally required to walk, stand, climb, balance, stoop, kneel, crouch, or crawl. The employee must occasionally lift and/or move up to 25 pounds. Specific vision abilities required by this job include close vision.
See All 65 Clinical Research Manager Jobs in Maryland
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Find JobsClinical Research Manager Jobs by City in Maryland
Where Maryland roles are concentrated, by current openings.
Rockville
5 jobsGaithersburg
3 jobsClinton
2 jobsSilver Spring
2 jobsAnnapolis
1 jobFrederick
1 jobPikesville
1 jobChevy Chase
1 jobHavre de Grace
1 jobClinical Research Manager Job Market in Maryland
A snapshot from current Maryland openings, updated as new roles post.
Who's Hiring
- Johns Hopkins University32
- Axle2
- Westat2
- Maryland Oncology2M
- The Emmes Company2
Top Industries Hiring
- Education11
- Science & Research2
- Healthcare & Medical Services2
- Staffing & Recruiting1
- Government & Public Sector1
What Maryland Employers Look For
The qualifications that appear most often in clinical research manager jobs across Maryland.
- Bachelor's or master's degree in life sciences, nursing, or a related clinical field required
- Certified Clinical Research Professional (CCRP) or ACRP certification strongly preferred by Maryland employers
- Minimum five years of clinical research experience including at least two years in a supervisory role
- Demonstrated knowledge of FDA regulations, ICH-GCP guidelines, and IRB submission processes
- Experience managing multi-site or Phase II through IV clinical trials from start-up to closeout
- Proficiency with electronic data capture systems such as Medidata Rave or Oracle Clinical
Clinical Research Manager Jobs in Maryland: Frequently Asked Questions
How do you become a clinical research manager in Maryland?
Most clinical research managers in Maryland hold at least a bachelor's degree in a life science, nursing, or public health field, with many employers preferring a master's. Maryland does not issue a state license specific to clinical research, so candidates advance by earning nationally recognized credentials such as the CCRP through the Society of Clinical Research Associates or the CCRC through the Association of Clinical Research Professionals, building years of coordinator-level experience, and demonstrating regulatory knowledge before moving into management roles at academic centers or biotech firms.
Which companies hire clinical research managers in Maryland?
Maryland clinical research manager roles are posted by Johns Hopkins University, Axle, and Westat and others right now, based on current listings on Migrate Mate as of October 2026. Maryland's density of federal health agencies and academic medical systems means many openings come from large institutions rather than pure-play staffing firms.
Which Maryland cities have the most clinical research manager jobs?
Baltimore, Bethesda, and Rockville lead Maryland for clinical research manager openings. Baltimore draws volume from Johns Hopkins Medicine and the University of Maryland Medical System, Bethesda and Rockville benefit from proximity to NIH and a dense biotech corridor in Montgomery County, and the broader DC suburbs add federal contractor and CRO demand that keeps smaller jurisdictions on the map.
Are there remote clinical research manager jobs in Maryland?
Yes, but they're less common than in purely desk-based fields because the role often requires on-site trial oversight, investigator visits, and staff supervision. About 67% of clinical research manager openings tied to Maryland are remote or hybrid as of October 2026, and those positions tend to cover study monitoring, regulatory document management, and vendor oversight rather than hands-on site operations.
How can I get hired as a clinical research manager in Maryland with little or no experience?
The most realistic entry path is a clinical research coordinator or research associate role at a Baltimore academic medical center, a Montgomery County CRO, or a federal contractor supporting NIH-affiliated studies. Johns Hopkins, University of Maryland Medical Center, and Westat all post entry-level research positions that build the protocol and regulatory experience hiring managers expect before promoting into management. Earning a CCRP credential and completing GCP training through a recognized program sharpens a candidate's profile even before accumulating years on the job.
Where can I find and apply to clinical research manager jobs in Maryland?
You can find and apply to clinical research manager jobs in Maryland on Migrate Mate, which lists current Maryland openings updated in real time. Search the listings to see roles that match your experience level, specialization, and preferred location within the state, then apply directly to the ones that fit your background.
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