Top 29 Clinical research coordinator Jobs in Chesapeake, Va

Clinical Research Coordinator
Odyssey Consulting —Naval Medical Center Portsmouth, VA
- $74,000 a year
- Full-time
- Microsoft Excel
- OSHA
- Patient monitoring
- Health savings account
- Paid holidays
Clinical Research Coordinator I
Velocity Clinical Research, Inc. —Suffolk, VA
- English
- Mid-level
- Ability to sit for extended periods
- Paid holidays
- Health insurance
Quick Apply
4d
Clinical Research Nurse/Coordinator
Virginia Oncology Associates —Norfolk, VA
- $47,964.80 - $128,939.20 a year
- Full-time
- Nursing
- Patient monitoring
- RN License
- 401(k)
Clinical Research Coordinator
Odyssey Systems Consulting Group, Ltd. —Portsmouth, VA
- $74,000 a year
- Full-time
- Microsoft Excel
- OSHA
- Patient monitoring
- Health savings account
- Paid holidays
PART TIME Clinical Research Coordinator I
TIDEWATER PHYSICIANS MULTISPECIALTY GROUP P C —Newport News, VA
- From $52,243 a year
- Part-time
- Ability to walk for extended periods
- Word processing
- HIPAA
5d
Registered Nurse (RN) Clinical Coordinator - Emergency Department (ED) - Harbour View Medical Center
Bon Secours —Suffolk, VA
- $38.63 - $61.82 an hour
- Full-time
- CPR Certification
- Nursing
- RN License
- Health savings account
- Disability insurance
Oncology Clinical Research Nurse/Coordinator
Virginia Oncology Associates —Norfolk, VA
- $47,964.80 - $128,939.20 a year
- Full-time
- Nursing
- Patient monitoring
- RN License
- 401(k)
Clinical Research Associate (CRA- Contract)
Beaufort LLC —Virginia Beach, VA
- Contract
- 5 years
- Bachelor's degree
- Travel
Quick Apply
Clinical Research Assistant
Velocity Clinical Research, Inc. —Hampton, VA
- Vital signs
- English
- High school diploma or GED
- Paid holidays
- Health insurance
Quick Apply
11d
Public Safety Clinical Coordinator
City of Virginia Beach —Virginia Beach, VA
- $68,328.00 - $105,892.80 a year
- Overtime
- Psychiatry
- High school
- 5 years
- Wellness program
- Paid holidays
5d
RN Clinical Coordinator - Hampton Rheumatology Specialists
Riverside Medical Group - Peninsula - Physician Specialists —Hampton, VA
- $76,400 - $105,050 a year
- Full-time
- CPR Certification
- Nursing
- RN License
Quick Apply
11d
RN Clinical Coordinator Home Health
EveryAge —Suffolk, VA
- $83,200 - $90,000 a year
- Nursing
- Mid-level
- Home Health
- Paid training
- Wellness program
Quick Apply
13d
RN Clinical Coordinator - Home Health
Chesapeake Regional Medical Center —Chesapeake, VA
- Nursing
- RN License
- Bachelor of Science
Quick Apply
RN Clinical Coordinator - 5 East Oncology
Chesapeake Regional Medical Center —Chesapeake, VA
- Nursing
- RN License
- Hospital
Quick Apply
RN Clinical Coordinator - Nursery/NICU (Night)
Chesapeake Regional Medical Center —Chesapeake, VA
- Nursing
- RN License
- Bachelor of Science
Quick Apply
RN Clinical Coordinator - ED (NIGHTS)
Chesapeake Regional Medical Center —Chesapeake, VA
- Nursing
- RN License
- PALS Certification
Quick Apply
RN Clinical Coordinator - Stepdown (WEEKEND ONLY)
Chesapeake Regional Medical Center —Chesapeake, VA
- Nursing
- RN License
- PALS Certification
Quick Apply
RN Clinical Coordinator - 3W: Med Surg Uro-GYN (NIGHTS)
Chesapeake Regional Medical Center —Chesapeake, VA
- Nursing
- RN License
- PALS Certification
Quick Apply
RN Clinical Coordinator - 2W: Cardiac/Telemetry (NIGHTS)
Chesapeake Regional Medical Center —Chesapeake, VA
- Nursing
- RN License
- Hospital
Quick Apply
RN Clinical Coordinator - 5E: MedSurg Oncology (Night)
Chesapeake Regional Medical Center —Chesapeake, VA
- Nursing
- RN License
- Hospital
Quick Apply

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Clinical Research Coordinator

Odyssey Consulting -
Naval Medical Center Portsmouth, VA

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Job Details

Full-time
$74,000 a year

Benefits

Health savings account
Paid holidays
Disability insurance
Health insurance
Dental insurance
Flexible spending account
Paid time off
Employee assistance program
Vision insurance
401(k) matching
Life insurance

Qualifications

Microsoft Excel
Patient monitoring
Windows
Bachelor's degree
Desktop applications
Productivity software
Medical terminology
Technical Proficiency

Full Job Description

Position Summary

Odyssey is seeking a Clinical Research Coordinator to support the Clinical Investigation Department (CID) at the Navy Medical Center, Portsmouth (NMCP) Virginia. The mission of the command is to support the national interests of the United States by providing professional education and development, providing quality patient care, being responsive and ready for deployment, and taking care of each other as shipmates. NMCP conducts biomedical research in general surgery, psychology, otolaryngology, pediatrics, nursing research, orthopedics, women’s health, and emergency medicine, which are relevant to the Graduate Medical Education Program.

Responsibilities

Duties include, but not limited to:

Provide research support for IRB and IACUC approved research protocols.
Support the Department Head of the CID, Directorate for Professional Education, NMCP.
Support the Department Head of CID and is accountable for research matters to the PIs of each research protocol in accordance with federal and local regulatory guidelines.
Use programs such as Word, Excel, etc., as well as clinical computer systems including Composite Health Care System (CHCS-I) and Armed Forces Health Longitudinal Technology Application (AHLTA).
For consultation, reporting, exchange of information, orientation support for the performance of duties, and to guide patients through a research protocol, will maintain and document contact with study subjects and research personnel from government agencies, granting agencies, industry sponsors.
Provide IRB/HRPP support to the PI in the development and implementation of recruitment strategies in accordance with IRB/HRPP requirements and approvals.
Screen recruited research subjects using protocol inclusion/exclusion criteria.
Refer eligible patients to the PI for final evaluation, enrollment, and randomization per protocol design after the informed consent process has taken place effectively, all subject questions are answered satisfactorily, and the process is documented.
Assist the research pharmacist with correct receipt, dispensation and accountability/documentation of investigational drugs per the sponsor protocol on Investigational Drug/Device Accountability.
Provide subjects with education on compliance, possible side effects, drug interactions and the importance of contacting the coordinator and study team members as applicable.
Assist with maintaining adequate inventory of study supplies, including drugs, and devices, and preparation of other study materials. These study materials include the informed consent document, case report forms (CRFs)/data collection forms (DCFs), enrollment logs, concomitant medication/adverse events logs and drug/device accountability logs.
Assist the PI by providing materials and tools necessary for the development of appropriate training of individuals involved in the execution of a study related to protocol requirements, schedule of visits, execution of research plan, and maintain documentation of training.
In collaboration with the PI, check on the performance of phlebotomies, electrocardiograms, vital signs, specimen collection and shipment, and other procedures as required by the protocol.
Observe universal precautions and OSHA standards when processing or handling specimens.
Obtain laboratory results and consult with the PI for follow-up care as per protocol.
Collect data in a timely and accurate manner and submit information to coordinating centers.
Report and document adverse events and unanticipated problems to governing agencies and sponsors as required by protocol and regulations.
Review compliance of research subject and complete documentation of status and progress. Respond to Assurance Specialist discrepancy/findings and, after consultation with PI, communicate approved recommendations.
Conduct telephone, face-to-face interviews or mail information for follow-up visits as per protocol. Maintain detailed documentation of the research study including subject study charts and databases as required by the protocol, and the Investigator’s File Binder or Regulatory Binder.
Prepare reports and other correspondence regarding the research protocol for the IRB, granting agencies, industry sponsors and other organizations as required by regulation and/or the protocol.
Interact on a regular basis with the PI and study team members regarding the conduct of the research study.
Attend conferences and other meetings as required by the protocol.
Return telephone calls from research participants within 48 hours and document interactions appropriately.
Work is performed in ambulatory care spaces and inpatient wards with some risk of exposure to infectious disease, for which gloves, masks, or gowns provided by the government entity may be required for safety reasons.
Maintain patient confidentiality in accordance with HIPAA and institutional regulations. Actively participate in CID departmental and command-wide research educational and training programs by providing instruction and presentation materials to assist research staff, as needed.
Actively participate in assurance assist visits and regulatory audits for protocol compliance.
Assist PI, research team members, and other staff in the preparation of and closeout of clinical research studies.
Collaborate with PI, study personnel and CID grants writer to source research funding for future protocols.

Qualifications

Minimum Required Qualifications:

Citizenship: Must be a US citizen

Clearance: Ability to obtain a Secret Clearance

Education: Bachelor’s Degree from an accredited college or university

Certifications:

Certified Clinical Trial Investigator (CCTI)
Certified Clinical Research Coordinator (CCRC)
Certified Clinical Research Professional (CCRP) from the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA).

Years’ experience:

A minimum of two (2) years as a Clinical Research Coordinator within the past five years OR Current certification as a Certified Clinical Trial Investigator (CCTI), Certified Clinical Research Coordinator (CCRC), Certified Clinical Research Professional (CCRP) from the Association of Clinical Research Professionals (ACRP) or the Society of Clinical Research Associates (SoCRA).
Minimum of two (2) to four (4) years of monitoring experience in a clinical research environment and administrative Institutional Review Board (IRB) experience.
Possess knowledge of medical terminology and clinical monitoring process and in depth therapeutic and protocol knowledge.
Ability to communicate effectively, both orally and in writing.
Possess effective organizational and analytical skills with ability to work independently and in a team environment.
Proficiency with Windows base computer systems, including Microsoft Windows and Microsoft Office Suites program.
Must possess the ability to complete research subject protection training developed by the Collaborative Institutional Training Initiative (CITTI), and additional protocol specific training, as required, within one month from start date

Preferred Qualifications:

Clearance: (ability to obtain) Secret Clearance

Additional Information:

Location: Navy Medical Center, Portsmouth (NMCP) Virginia

On-site (local candidates only)

#LI-JC1

Company Overview

Odyssey is a world-class technical, engineering, and integration company serving the warfighting ecosystem with airborne integration, ISR, C2, and warfighter readiness capabilities. Odyssey meets the military’s operational needs by integrating layered defense systems from equipment, technology, and services to data, information, and business operations. We streamline defense acquisition and sustainment, engineering the technical battlefield with domain-specific proficiency to ensure lethality. Odyssey is dedicated to excellent contract execution, peak organizational performance, and fostering a workplace built on employee care.

Odyssey is proud to live out our core values of commitment, ambition, and respect in our work and communities through OdysseyCares, a philanthropic group focused on giving back through direct donations, an employer match program, and volunteering events.

Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities

Please Note:

Final compensation for this position will be determined by various factors such as the Federal Government contract labor categories and contract wage rates, relevant work experience, specific skills and competencies, geographic location, education, and certifications.

This position is filled through continuous recruitment and will remain open until a sufficient pool of applications has been received.

Hired applicants may be eligible for benefits, including but not limited to, medical, dental, vision, life insurance, Tricare supplement, short-term disability, long-term disability, 401(k) match, flexible spending accounts, health savings accounts, employee assistance program, learning and development benefit, paid time off, and holidays.

Odyssey Benefits

Apply Now

Refine Your Search

clinical research coordinator jobs in chesapeake, va

Clinical Research Coordinator

Clinical Research Coordinator I

Clinical Research Nurse/Coordinator

Clinical Research Coordinator

PART TIME Clinical Research Coordinator I

Registered Nurse (RN) Clinical Coordinator - Emergency Department (ED) - Harbour View Medical Center

Oncology Clinical Research Nurse/Coordinator

Clinical Research Associate (CRA- Contract)

Clinical Research Assistant

Public Safety Clinical Coordinator

RN Clinical Coordinator - Hampton Rheumatology Specialists

RN Clinical Coordinator Home Health

RN Clinical Coordinator - Home Health

RN Clinical Coordinator - 5 East Oncology

RN Clinical Coordinator - Nursery/NICU (Night)

RN Clinical Coordinator - ED (NIGHTS)

RN Clinical Coordinator - Stepdown (WEEKEND ONLY)

RN Clinical Coordinator - 3W: Med Surg Uro-GYN (NIGHTS)

RN Clinical Coordinator - 2W: Cardiac/Telemetry (NIGHTS)

RN Clinical Coordinator - 5E: MedSurg Oncology (Night)

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