10 Clinical Research Coordinator Jobs in Portsmouth, VA
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The Henry M. Jackson Foundation for the Advancement of Military Medicine
Portsmouth, VA | Full Time
$58k-78k (estimate)
4 Months Ago
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Clinical Research Coordinator
$65k-89k (estimate)
Full Time | IT Outsourcing & Consulting
3 Weeks Ago
Odyssey Systems is Hiring a Clinical Research Coordinator Near Portsmouth, VA
Position SummaryOdyssey Systems is currently seeking a Clinical Research Coordinator to support the Clinical Investigation Department (CID) at the Navy Medical Center, Portsmouth (NMCP) Virginia.
ResponsibilitiesDuties includ e, but not limited to:
Clearance : Ability to obtain a Secret Clearance
Education: Bachelor’s Degree from an accredited college or university
Certifications
Additional Information Location: Navy Medical Center, Portsmouth (NMCP) Virginia
Currently remote, must be within a commutable distance as onsite work will be required upon update from Base Command.
jobs in Portsmouth medical jobs in Virginia crc government jobs navy jobs cleared medical jobs
Company OverviewOdyssey Systems Consulting Group, is an innovative small business committed to providing world-class technical, management, and training support services to government and public sector clients. We focus on people, processes, and performance to deliver superior results. Since our inception in 1997, our commitment to mission success and customer satisfaction has been recognized with exponential growth and exceptional past performance ratings. We accept challenging assignments and drive projects from the planning stages, through implementation, and into operations and support.
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.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
ResponsibilitiesDuties includ e, 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.
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).
- 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
Additional Information Location: Navy Medical Center, Portsmouth (NMCP) Virginia
Currently remote, must be within a commutable distance as onsite work will be required upon update from Base Command.
jobs in Portsmouth medical jobs in Virginia crc government jobs navy jobs cleared medical jobs
Company OverviewOdyssey Systems Consulting Group, is an innovative small business committed to providing world-class technical, management, and training support services to government and public sector clients. We focus on people, processes, and performance to deliver superior results. Since our inception in 1997, our commitment to mission success and customer satisfaction has been recognized with exponential growth and exceptional past performance ratings. We accept challenging assignments and drive projects from the planning stages, through implementation, and into operations and support.
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.
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
Job Summary
JOB TYPE
Full Time
INDUSTRY
IT Outsourcing & Consulting
SALARY
$65k-89k (estimate)
POST DATE
05/23/2024
EXPIRATION DATE
07/17/2024
WEBSITE
odysseyconsult.com
HEADQUARTERS
COLORADO SPRINGS, CO
SIZE
200 - 500
FOUNDED
1997
TYPE
Private
CEO
JON DOWLING
REVENUE
$50M - $200M
INDUSTRY
IT Outsourcing & Consulting
Related Companies
About Odyssey Systems
Odyssey is a provider of program management, system engineering and medical research services for the government and private sectors.
Show more
The job skills required for Clinical Research Coordinator include Clinical Research, Clinical Trial, Presentation, Initiative, Data Collection, Planning, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Research Coordinator. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Research Coordinator. Select any job title you are interested in and start to search job requirements.
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The following is the career advancement route for Clinical Research Coordinator positions, which can be used as a reference in future career path planning. As a Clinical Research Coordinator, it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Coordinator. You can explore the career advancement for a Clinical Research Coordinator below and select your interested title to get hiring information.
The Henry M. Jackson Foundation for the Advancement of Military Medicine
Full Time
$58k-78k (estimate)
4 Months Ago
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