Clinical Research Manager Jobs in Bethesda, MD
Clinical Research Manager jobs in Bethesda are in strong demand, with openings concentrated in the NIH campus corridor, downtown Bethesda, and the Pike & Rose district across pharmaceutical, biotech, and federal health research sectors. Employers hiring right now include Westat, Comprehensive Research Solutions, and The Henry M. Jackson Foundation for the Advancement of Military Medicine. See the openings below and apply to the ones that match your experience.
Find JobsOverview
Open roles65
Top employerWestat
Work type63% Hybrid
Top credentialBachelor's degree
Companies hiring9
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
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
C
Clinical Protocol Analyst (Clinical Research Associate)
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C
Added 1w ago
Comprehensive Research Solutions, LLC
Clinical Protocol Analyst (Clinical Research Associate)
Bethesda, Maryland
Added 1w ago
Bilingual Clinical Research Patient Coordinator
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Added 3w ago
GAP Solutions, Inc.
Bilingual Clinical Research Patient Coordinator
Bethesda, Maryland
Added 3w ago
Biostatistician (Senior Statistical Associate) - Clinical Research
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Added 3w ago
Westat
Biostatistician (Senior Statistical Associate) - Clinical Research
Bethesda, Maryland
Added 3w 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.
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Find JobsClinical Research Manager Job Market in Bethesda
Who's Hiring
- Westat11
- Comprehensive Research Solutions11C
- The Henry M. Jackson Foundation for the Advancement of Military Medicine11
- Chenega Corporation5
- GAP Solutions5
Clinical Research Manager Jobs in Bethesda: Frequently Asked Questions
How do I get a clinical research manager job in Bethesda?
Focus your search on Bethesda's NIH-adjacent employers, contract research organizations operating near the federal campus, and the biotech and pharma companies concentrated downtown and along Rockville Pike. Candidates with direct experience managing FDA-regulated clinical trials, familiarity with federal research protocols, or prior work with NIH-funded studies have a clear edge here. Networking through local biomedical research associations and attending events tied to the Montgomery County life sciences community also opens doors that online applications alone do not.
Which companies hire clinical research managers in Bethesda?
Companies currently hiring clinical research managers in Bethesda include Westat, Comprehensive Research Solutions, and The Henry M. Jackson Foundation for the Advancement of Military Medicine, per current listings on Migrate Mate as of October 2026. Bethesda's employer mix leans heavily toward federal health agencies, their contracted research partners, and specialty pharmaceutical firms drawn to the city by proximity to NIH headquarters.
Are there remote clinical research manager jobs in Bethesda?
Yes, though availability depends on the role, since clinical research managers overseeing active trial sites or direct patient-facing operations typically need to be on-site. About 63% of clinical research manager openings tied to Bethesda are remote or hybrid as of October 2026, with remote work most common in protocol development, data management oversight, and regulatory affairs coordination rather than hands-on site management.
How can I get a clinical research manager job in Bethesda with little or no experience?
The most realistic entry path in Bethesda is through a clinical research coordinator or clinical trial associate role at one of the contract research organizations or academic medical centers operating near the NIH campus. These positions build the trial management and regulatory documentation skills that local employers require before moving someone into a manager seat. Candidates who have completed an internship or research assistant position within an NIH-affiliated program are consistently preferred by Bethesda hiring teams over applicants without that federal research exposure.
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