Clinical Research Nurse
Washington, DC · On-site
The Research Nurse is responsible for managing at least 15 trials out of the overall portfolio of ... At least one (1) year clinical trials research experience preferred * Knowledge of medical ...
Washington, DC · On-site
The Research Nurse is responsible for managing at least 15 trials out of the overall portfolio of ... At least one (1) year clinical trials research experience preferred * Knowledge of medical ...
Washington, DC · On-site
The Research Nurse is responsible for managing at least 15 trials out of the overall portfolio of ... At least one (1) year clinical trials research experience preferred * Knowledge of medical ...
Washington, DC · On-site
The Research Nurse is responsible for managing at least 15 trials out of the overall portfolio of ... At least one (1) year clinical trials research experience preferred * Knowledge of medical ...
Washington, DC · On-site
The Research Nurse is responsible for managing at least 15 trials out of the overall portfolio of ... At least one (1) year clinical trials research experience preferred * Knowledge of medical ...
Washington, DC · On-site
The Research Nurse is responsible for managing at least 15 trials out of the overall portfolio of ... At least one (1) year clinical trials research experience preferred * Knowledge of medical ...
Washington, DC · On-site
The Research Nurse is responsible for managing at least 15 trials out of the overall portfolio of ... At least one (1) year clinical trials research experience preferred * Knowledge of medical ...
Washington, DC · On-site
$20.16 - $31.30/hr
Work Interactions The Research Coordinator will work under the direct supervision of a nurse who will delegate appropriate tasks and report directly to CRU Nurse Manager. They will provide clinical ...
Washington, DC · On-site
$20.16 - $31.30/hr
Work Interactions The Research Coordinator will work under the direct supervision of a nurse who will delegate appropriate tasks and report directly to CRU Nurse Manager. They will provide clinical ...
Washington, DC · On-site
$27.50 - $36.75/hr
Requirements Job Overview The Clinical Research Coordinator 2 (CRC2) is responsible for managing ... Coordination and management of such studies is both a dynamic and demanding responsibility that ...
Washington, DC · On-site
$27.50 - $36.75/hr
Requirements Job Overview The Clinical Research Coordinator 2 (CRC2) is responsible for managing ... Coordination and management of such studies is both a dynamic and demanding responsibility that ...
Manage the contract's clinical informatics scope, staffing, budget (as applicable), milestones, deliverables, and risk management. * Produce high-quality documentation (program plans, governance ...
Manage the contract's clinical informatics scope, staffing, budget (as applicable), milestones, deliverables, and risk management. * Produce high-quality documentation (program plans, governance ...
Washington, DC · On-site +1
Manage the contract's clinical informatics scope, staffing, budget (as applicable), milestones, deliverables, and risk management. * Produce high-quality documentation (program plans, governance ...
Washington, DC · On-site +1
Manage the contract's clinical informatics scope, staffing, budget (as applicable), milestones, deliverables, and risk management. * Produce high-quality documentation (program plans, governance ...
Proven leadership experience managing cross-functional and/or senior project teams; Demonstrated success in strategy development and execution in both clinical research and clinical development ...
Proven leadership experience managing cross-functional and/or senior project teams; Demonstrated success in strategy development and execution in both clinical research and clinical development ...
Proven leadership experience managing cross-functional and/or senior project teams; Demonstrated success in strategy development and execution in both clinical research and clinical development ...
Proven leadership experience managing cross-functional and/or senior project teams; Demonstrated success in strategy development and execution in both clinical research and clinical development ...
Clinical Research Rater (Psychiatry/CNS) Location: Fairfax, VA Job Type: Full-Time or Part-Time ... Collaborate with investigators, project managers, and research staff to ensure compliance with FDA ...
Quick apply
Clinical Research Rater (Psychiatry/CNS) Location: Fairfax, VA Job Type: Full-Time or Part-Time ... Collaborate with investigators, project managers, and research staff to ensure compliance with FDA ...
Gaithersburg, MD · On-site
$180 - $240/hr
Lead the work with Line Managers toidentifyresource need and secure resources to ensure flexible andtimelyformation of the Clinical Research & Development Teams and progression of deliverables
Gaithersburg, MD · On-site
$180 - $240/hr
Lead the work with Line Managers toidentifyresource need and secure resources to ensure flexible andtimelyformation of the Clinical Research & Development Teams and progression of deliverables
Lead the work with Line Managers toidentifyresource need and secure resources to ensure flexible andtimelyformation of the Clinical Research & Development Teams and progression of deliverables ...
Lead the work with Line Managers toidentifyresource need and secure resources to ensure flexible andtimelyformation of the Clinical Research & Development Teams and progression of deliverables ...
Washington, DC · On-site
$67K/yr
Clinical Research Manager * Disease Group members: Principal Investigators, Physicians, Clinicians * Clinical Research Management Office (CRMO) members: Clinical Research Nurses, Clinical Research ...
Washington, DC · On-site
$67K/yr
Clinical Research Manager * Disease Group members: Principal Investigators, Physicians, Clinicians * Clinical Research Management Office (CRMO) members: Clinical Research Nurses, Clinical Research ...
Manage activities associated with audits to ensure compliance with GCP, ICH, AZ standards, and ... May mentor and manage clinical research professionals and study teams, providing performance ...
Manage activities associated with audits to ensure compliance with GCP, ICH, AZ standards, and ... May mentor and manage clinical research professionals and study teams, providing performance ...
Gaithersburg, MD · On-site
$120 - $180/hr
Manage activities associated with audits to ensure compliance with GCP, ICH, AZ standards, and ... May mentor and manage clinical research professionals and study teams, providing performance ...
Gaithersburg, MD · On-site
$120 - $180/hr
Manage activities associated with audits to ensure compliance with GCP, ICH, AZ standards, and ... May mentor and manage clinical research professionals and study teams, providing performance ...
$22.50 - $25/hr
Headquartered in Birmingham, No Resistance is a clinical trial site management organization that ... In this role, you'll play a pivotal part in the implementation and execution of clinical research ...
$22.50 - $25/hr
Headquartered in Birmingham, No Resistance is a clinical trial site management organization that ... In this role, you'll play a pivotal part in the implementation and execution of clinical research ...
Greenbelt, MD · On-site
$22.50 - $25/hr
Headquartered in Birmingham, No Resistance is a clinical trial site management organization that ... In this role, you'll play a pivotal part in the implementation and execution of clinical research ...
Quick apply
Greenbelt, MD · On-site
$22.50 - $25/hr
Headquartered in Birmingham, No Resistance is a clinical trial site management organization that ... In this role, you'll play a pivotal part in the implementation and execution of clinical research ...
Greenbelt, MD · On-site
$22.50 - $25/hr
Headquartered in Birmingham, No Resistance is a clinical trial site management organization that ... In this role, you'll play a pivotal part in the implementation and execution of clinical research ...
Greenbelt, MD · On-site
$22.50 - $25/hr
Headquartered in Birmingham, No Resistance is a clinical trial site management organization that ... In this role, you'll play a pivotal part in the implementation and execution of clinical research ...
What You Will Do Expert in the field of drug research and development, contributing deep specialist ... Experience managing and interpreting the results of clinical trials. Knowledge of autoimmune ...
What You Will Do Expert in the field of drug research and development, contributing deep specialist ... Experience managing and interpreting the results of clinical trials. Knowledge of autoimmune ...
What You Will Do Expert in the field of drug research and development, contributing deep specialist ... Experience managing and interpreting the results of clinical trials. Knowledge of autoimmune ...
What You Will Do Expert in the field of drug research and development, contributing deep specialist ... Experience managing and interpreting the results of clinical trials. Knowledge of autoimmune ...
$51K - $64.2K
3% of jobs
$64.2K - $77.5K
13% of jobs
$82.8K is the 25th percentile. Wages below this are outliers.
$77.5K - $90.7K
22% of jobs
The median wage is $101.9K / yr.
$90.7K - $103.9K
14% of jobs
$103.9K - $117.2K
16% of jobs
$122.9K is the 75th percentile. Wages above this are outliers.
$117.2K - $130.4K
16% of jobs
$130.4K - $143.7K
7% of jobs
$143.7K - $156.9K
6% of jobs
$156.9K - $170.1K
2% of jobs
$170.1K - $183.4K
0% of jobs
$183.4K - $196.6K
0% of jobs
$51K
$111.7K
$196.6K
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Posted 14 days ago
Georgetown University comprises two unique campuses in the nation’s capital. With the Hilltop Campus located in the heart of the historic Georgetown neighborhood, and the Capitol Campus, just minutes from the U.S. Capitol and U.S. Supreme Court, Georgetown University offers rigorous academic programs, a global perspective, and unparalleled opportunities to engage with Washington, D.C. Our community is a close-knit group of remarkable individuals driven by intellectual inquiry, a commitment to social justice, and a shared dedication to making a difference in the world.
Requirements
Job Overview
The Clinical Research nurse, Lombardi Cancer Center – Georgetown University, is a position in the benign Hematology clinical research program. Under the guidance and supervision of the Principal Investigator (PI), ensures the integrity and quality of clinical trials are maintained and conducted in accordance w/ federal, state, and local regulations, Institutional Review Board (IRB) approvals, and Georgetown University policies and procedures. This position is primarily responsible for the accurate completion of visit procedures and collection of information from study patients according to protocols, and for protecting the health, safety, and welfare of research participants. The clinical trial nurse also acts as study coordinator for research studies.
Additional duties include but are not limited to:
Ensures compliance with each study’s protocol. Participates in recruitment and selection of study participants.
Provides patient education and medical information to study patients
Supports the regulatory staff in the maintenance of regulatory documents
Communicates and collaborates w/ study team including internal and external parties
Develops accurate source materials
Work Interactions
As an employee of Georgetown University, the Hematology Research program directly supports the University’s mission of cura personalis. Clinical Trials offer a unique opportunity for a patient to receive personalized and comprehensive care in a manner that they may not experience otherwise as a patient. Per the requirements of each clinical trial protocol, the research personnel are required to be the main point of contact for a patient in a clinical trial and must respond to inquiries from any patient within 24 hours. The research nurse is instructed and required to maintain regular contact with each patient in their respective trials, because it is an FDA requirement to report adverse events in a timely manner, no matter the severity. As such, clinical trial patients develop close relationships with the research nurse for a trial, which provides unprecedented access to care when necessary.
Operationally, the Research Nurse coordinates with other centers such as the Clinical Research Operations Office (CROO), the Clinical Research Unit (CRU), the Research Pharmacy, the Radiology Center, Center of Medicine and Bone marrow transplant. By interacting with other centers within the GUMC, the position indirectly supports research-related operations in centers ancillary to hematology.
On a daily basis, the Research Nurse will report to the Center Administrator and Principal Investigator. The Research Nurse is part of a robust team comprised of 8 study team members (including the Research Nurse, the Administrator, 3 Principal Investigators, a Study Coordinator, Hemophilia Research Nurse and a Regulatory Coordinator. The Research Nurse is responsible for managing at least 15 trials out of the overall portfolio of approximately 33 ongoing trials within our center. The portfolio consists of hematologic diseases, gene therapy and immunotherapy protocols. While the Research Nurse's primary direct report is to the Center Administrator, the Research Nurse will also provide project-specific deliverables to others such as, the PI for each trial, study team members, and to the sponsor contact (e.g., the study monitor appointed by the sponsor for each trial).
Requirements and Qualifications
Valid RN license
Bachelor of Nursing degree
Two (2) years of recent clinical nursing experience in a hospital, clinic or similar health care setting
Nursing competency skills per scope of practice (i.e., performing vital signs, nursing assessments, performing ECG/EKG, administering injections, etc.)
At least one (1) year clinical trials research experience preferred
Knowledge of medical terminology, drug calculation skills, clinical medicine, clinical trials and GCP concepts
Detail oriented and meticulous in all aspects of work
Strong follow through skills and ability to proactively identify and solve problems; demonstrated initiative is imperative
Must have professional demeanor, strong communication skills with the public as well as physicians and co-workers
Ability to work well independently as well as in team environment
Strong interpersonal, customer service and multi-tasking skills are critical
Must be proficient in Microsoft Office Word and Excel, electronic health systems and databases used in research environment, or have a willingness to learn and demonstrate proficiency within six months of hire
Possess the ability to work well under pressure, multi-task, and manage deadlines
Knowledge of GCP, federal, state, and local regulations, including HIPAA policies and procedures
Work Mode Designation
This position has been designated as On-Campus. Please note that work mode designations are regularly reviewed in order to meet the evolving needs of the University. Such review may necessitate a change to a position’s mode of work designation. Complete details about Georgetown University’s mode of work designations for staff positions can be found on the Center of Human Resources website: https://hr.georgetown.edu/mode-of-work-designation .
Pay Range:
The projected salary or hourly pay range for this position which represents the full range of anticipated compensation is:
$54,616.00 - $100,493.33
Compensation is determined by a number of factors including, but not limited to, the candidate’s individual qualifications, experience, education, skills, and certifications, as well as the University’s business needs and external factors.
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Submission Guidelines:
Please note that in order to be considered an applicant for any position at Georgetown University you must submit a resume for each position of interest for which you believe you are qualified. Documents are not kept on file for future positions.
Need Assistance:
If you are a qualified individual with a disability and need a reasonable accommodations for any part of the application and hiring process, please visit the Office for Equal Opportunity Compliance website for general information about requesting accommodations (https://oeoc.georgetown.edu/ada/) , as well as information about requesting accommodations specifically for applicants (https://oeoc.georgetown.edu/ada/applicants/) . You also can also contact the Office for Equal Opportunity Compliance at (202) 687-4798 or oeoc@georgetown.edu .
Need some assistance with the application process? Please call 202-687-2500. For more information about the suite of benefits, professional development and community involvement opportunities that make up Georgetown's commitment to its employees, please visit the Georgetown Works website (https://georgetownworks.georgetown.edu/) .
EEO Statement:
GU is an Equal Opportunity Employer (https://policymanual.hr.georgetown.edu/200-hiring-and-employment/201-equal-employment-opportunity-affirmative-action/) . All qualified applicants are encouraged to apply, and will receive consideration for employment without regard to age, citizenship, color, disability, family responsibilities, gender identity and expression, genetic information, marital status, matriculation, national origin, race, religion, personal appearance, political affiliation, sex, sexual orientation, veteran status, or any other characteristic protected by law (https://georgetown.box.com/s/jkc3kxwrf56e1n2km0jh1vj09fvanw70) .
Benefits:
Georgetown University offers a comprehensive and competitive benefit package that includes medical, dental, vision, disability and life insurance, retirement savings, tuition assistance, work-life balance benefits, employee discounts and an array of voluntary insurance options. You can learn more about benefits and eligibility on the Department of Human Resources website (https://benefits.georgetown.edu/staff/enrolling/) .