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Added 4 mins ago
Salesforce Go-to-Market Leader, Enterprise Capability - PNW
Slalom LLC
Seattle, WA
At the heart of Slalom's Enterprise Capability is a bold ambition: to design and deliver intelligent, human-centered business applications that empower organizations to serve their…
Added 4 mins ago
Enterprise Salesforce - Technical Architect
Slalom LLC
Seattle, WA
…Boomi, and Workato, we deliver scalable solutions that unify data, streamline operations, and turn insights into action. More than technologists, we connect strategy to execution by…
Added 12 mins ago
Solutions Architect - Networking
DataVizion
Urbandale, IA
DataVizion is hiring a Solutions Architect to lead the design, sale, and delivery handoff of network and security solutions for our clients. The stack is HPE Aruba Networking (AOS-CX, Aruba…
Added 19 mins ago
Director of Finance
DefinedTalent
Asbury Park
Design and implement a grant financial management framework including budget tracking templates, draw-down schedules, and funder reporting workflows
Added 19 mins ago
Senior Biostatistician
DefinedTalent
Remote, United States
DefinedTalent is looking for a Sr. Biostatistician to join one of their clients that is transforming clinical data workflows with multi agent ai and automation; cutting cycle times,…
Added 23 mins ago
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DOC East Moline CC Corrections Leisure Activity Specialist IV
State of Illinois
East Moline, IL
- $7,239 to $10,440 USD / month
…art education, fine arts, studio arts, graphics, color and design, music, theater, or speech and…
Added 26 mins ago
MM
Performance Leader, 2nd shift
Moog Military Aircraft LLC
Torrance, CA
- $90,000 to $130,000 CAD / year
…our production team supervising Assembly and Test area with data driven individual Reporting to the Process Manager, you will have an onsite 9/80 work schedule in Torrance,…
Added 29 mins ago
J
IM Transcend Deployment Lead Analyst
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Remote, United States
- $96,000 to $155,250 USD / year
…technology, and business teams, you will support system deployment, data migration, testing, and business adoption. This role offers the opportunity to contribute to a large-scale…
Added 36 mins ago
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Spring 2027 Central Unified Assistant Site Lead (Management)
CALIFORNIA TEACHING FELLOWS FOUNDATION
Fresno, CA
- $25 USD / hour
…program goals and safety standards. From assisting with essential data entry and reporting to stepping in to lead activities, you are a key leader on site who helps bridge the gap between…
Added 36 mins ago
CT
Spring 2027 West Fresno County Assistant Site Lead (Management)
CALIFORNIA TEACHING FELLOWS FOUNDATION
Fresno, CA
- $22 to $25 USD / hour
…program goals and safety standards. From assisting with essential data entry and reporting to stepping in to lead activities, you are a key leader on site who helps bridge the gap between…
Added 38 mins ago
Mobile Program Manager (48196)
Dilkon Medical Center | Winslow Indian Health Care
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Plans, implements, and evaluates all aspects of mobile health services, including annual budgeting, programmatic design, and stakeholder engagement.
Added 39 mins ago
Manager, Project Management - Community Engagement
Quality Technology Services, LLC
United States
As a global leader in digital infrastructure, QTS designs, builds and operates advanced data centers that support strategic AI, cloud and digital transformation initiatives. We are driven…
Added 41 mins ago
Co-founder in Residence, Next generation insecticides and pest control
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Added 41 mins ago
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Added 41 mins ago
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AI Connect Outside Plant Associate Director
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Basking Ridge, NJ · Bloomington, CA · Irving, TX · Houston, TX · West Jordan, UT · Temple Terrace, FL · Minneapolis, MN · Walnut Creek, CA · Indianapolis, IN
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Working knowledge of modern OSP design platforms, intelligent permitting software, and spatial data analytics tools.

Chenega Corp

Clinical Research Nurse

Bethesda, MD, United States

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Job details

Apply by: Nov 4, 2027
Posting language: English
Posted: Nov 4, 2026

Original job description

Overview

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

Responsibilities

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.)

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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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More about this job

Skills

Clinical research
Research
Critical thinking
Regulatory compliance
Clinical trials
Documentation
Document management
Data management
Computer technology
Decision making
Counselling
Scheduling
Patient care
Reporting
Infection prevention and control
Interact verbally in English
Computer skills

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