7 Research jobs in Hampton

**ManTech** seeks a motivated, career and customer-oriented **Senior Operations Research Analyst** to join our team in **Hampton, VA, Langley Air Force Base.** This is an onsite position.
ManTech looks for this qualified candidate that augments and assists the military and civilian staff in producing analysis to support Air Force acquisition decisions and must have Air Combat Aircraft experience.
**Responsibilities include but not limited to:**
+ Conduct and participate in short notice as well as long-term analytical studies and assessments using a variety of tools and techniques to include qualitative, spreadsheet, and computer simulation-based analyses
+ Lead and assist in the development of analysis plans for trade-off studies of Air Force combat aircraft and weapon requirements, modernization, and new acquisitions. Typical studies include, weapon capability analyses, aircraft survivability analyses, current and future combat aircraft inventory requirement analyses, and weapon acquisition analyses
+ Use available data, subject matter expert knowledge, and best judgement, create and maintain input data for computer simulations including, but not limited to, Advanced Framework for Simulation, Integration, and Modeling (AFSIM), Brawler Air Combat Simulation, Combat Forces Assessment Model (CFAM), Weapons Effects Analysis and Probability Software (WEAPS), and Joint Munitions Effectiveness Manual (JMEM) Joint Weaponeering System (JWS)
+ Run computer simulations and analyze output data, verify and validate the results, and adjust simulation inputs as required to align output with actual and/or expected results in a real-world environment
+ Present analysis of simulation output to include insights, conclusions, and recommendations in written documents and verbal briefings for review by Air Force decision makers
+ Attend and participate in meetings both locally and at other locations as a subject matter expert on air combat analysis and Air Combat Command Analysis Division's analytic capability
+ Complete computer based and in person training as required by the government and company policy.
**Minimum Requirements:**
+ Bachelor of Science degree in related field
+ 5+ years of experience in analysis and modeling of modern combat aircraft and other airborne systems
+ Collecting and establishing the pedigree of input data, conducting risk analysis; model manipulation and modification
**Preferred Requirements:**
+ Experience with AFSIM or Brawler Air Combat Simulation
+ Experience in Air Combat (preferably Air-to-Air), fighter aircraft weapons systems, and weapons employment
+ Experience developing study plans that include background, purpose of study, scope/limitations, critical assumptions and constraints, measures of effectiveness, study parameters and variables, methodology description, data requirements and schedule
+ Experience in programming in C/C++, Fortran, R, Python, MATLAB, and SQL and using Microsoft Office products
**Clearance Requirements:**
+ US Citizenship required and an active Secret security clearance with the ability to obtain and maintain a Top-Secret clearance with Sensitive Compartmented Information (TS/SCI) eligibility
**Physical Requirements:**
+ Must be able to remain in a stationary position 50%
+ Constantly operates a computer and other office productivity machinery, such as a calculator, copy machine and computer printer
ManTech International Corporation, as well as its subsidiaries proactively fulfills its role as an equal opportunity employer. We do not discriminate against any employee or applicant for employment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
If you are a qualified individual with a disability and require a reasonable accommodation to apply for a position with ManTech through its online applicant system, please email us at and provide your name and contact information.

Overview

The Clinical Research Coordinator provides complete management of the clinical trials for the Department of Obstetrics and Gynecology, including research in the areas of Maternal Fetal Medicine, Obstetrics, Gynecology, and Urogynecology.  The coordinator acts as liaison between the academic community, local community, multiple government agencies and/or commercial sponsors and the Department to facilitate all clinical and practical aspects of the clinical trial.  The coordinator, working independently, interacts with members of the unit to promote the goals of research, education, and patient care as defined in the mission statement of the Department.  Along with the investigator, the Clinical Research Coordinator will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study. In addition, the Clinical Research Coordinator is responsible for all data and source documentation, adverse experience reporting, and maintenance of complete regulatory file.  The coordinator is available to answer questions or evaluate symptoms and/or problems of patients in trials using sound clinical judgment to suggest additional referrals or appropriate follow-up.  Weekend and holiday call rotation may be necessary to perform clinical procedures, if required by specific protocols.  The coordinator manages multiple complex projects simultaneously with overlapping critical time frames, assigning priorities and delegating work appropriately.

Responsibilities

Possesses a full understanding of the clinical research process, study designs and regulatory standards of Good Clinical Practice and adheres to standards for scientific integrity mandating honest and truthful behavior in collecting and interpreting data for patients and sponsors

Supervises clinical research related activities including registration, maintenance and submission of patient data; pathology and laboratories results; drug dispensing; patient compliance; study results; adverse events; and follow up

Independently conducts, analyzes and evaluates all clinical research activities and makes recommendations to principal investigators or designated persons for any required changes

Maintains historical references by facilitating entry, editing, reviewing, management, reporting, and documentation of clinical trials data

Orders investigational drugs and/or devices as needed for protocol purposes and maintains inventories of drugs and devices to ensure that federal guidelines are met

Develops consent forms consistent with Food and Drug Administration (FDA), Institutional Review Board (IRB), and sponsor requirements

Maintains data from clinical studies in order to prepare interim, annual, and close out reports, and to provide statistical information on all clinical research protocols as required by the IRB, sponsor, and department

Maintains responsibility for updating Protocol, Regulatory Binders with addenda, amendments, closure notices, severe adverse drug reaction reports, and other FDA regulated documentation

Evaluates potential volunteers on an individual basis and obtains in depth medical history as related to study inclusion/exclusion criteria

Meets personally with patient volunteers to explain study requirements, and obtains informed consent prior to study screening

Organizes exam rooms in preparation for participants’ exams and procedures, determining equipment and other supplies

Assist with physical exams, endometrial and cervical biopsy, ultrasound, pap smears, colposcopy, catheterization, contraceptive rod insertion and removal, cervical mucus checks, post coital exams, and other procedures as required by protocols

Dispenses medication and educates patients on the correct method of administration of study drug and/or device, and documentation of pertinent medical information required

Provides health education to patient volunteers and encourages interventions for healthy living

Identifies potential disease processes and brings to physicians’ attention for evaluation, diagnosis and treatment

Provides counseling to patients in regards to laboratory results, side effects, etc., and suggests required follow up

Orchestrates protocol specific patient assessment throughout duration of study and any additional visits necessary to evaluate the health and safety of participants

Attends off site patient care visits at other laboratories, pharmacies, doctors’ offices, and hospital departments, to assess and evaluate participants according to protocol requirements

Oversees patients’ adherence to study requirements and makes necessary adjustments to ensure compliance with protocol (medication administration, diary card completion, concomitant medications, and adverse events)

Maintains proficiency in phlebotomy skills, intramuscular injections, ECG, and other clinical skills

Qualifications

Bachelor’s degree in nursing.  Prior nursing experience in research projects.  Must be licensed RN in Virginia. Ambulatory care and Clinical experience in family medicine desired. Customer service-oriented individual is required.

Location : Location US-VA-Norfolk

**MANTECH** seeks a motivated, career and customer-oriented **Senior Operations Research Analyst** to join our team in **Hampton, VA, Langley Air Force Base.** This is an onsite position.
ManTech looks for this qualified candidate that augments and assists the military and civilian staff in producing analysis to support Air Force acquisition decisions and must have Air Combat Aircraft experience.
**Responsibilities include but not limited to:**
+ Conduct and participate in short notice as well as long-term analytical studies and assessments using a variety of tools and techniques to include qualitative, spreadsheet, and computer simulation-based analyses
+ Lead and assist in the development of analysis plans for trade-off studies of Air Force combat aircraft and weapon requirements, modernization, and new acquisitions. Typical studies include, weapon capability analyses, aircraft survivability analyses, current and future combat aircraft inventory requirement analyses, and weapon acquisition analyses
+ Use available data, subject matter expert knowledge, and best judgement, create and maintain input data for computer simulations including, but not limited to, Advanced Framework for Simulation, Integration, and Modeling (AFSIM), Brawler Air Combat Simulation, Combat Forces Assessment Model (CFAM), Weapons Effects Analysis and Probability Software (WEAPS), and Joint Munitions Effectiveness Manual (JMEM) Joint Weaponeering System (JWS)
+ Run computer simulations and analyze output data, verify and validate the results, and adjust simulation inputs as required to align output with actual and/or expected results in a real-world environment
+ Present analysis of simulation output to include insights, conclusions, and recommendations in written documents and verbal briefings for review by Air Force decision makers
+ Attend and participate in meetings both locally and at other locations as a subject matter expert on air combat analysis and Air Combat Command Analysis Division's analytic capability
+ Complete computer based and in person training as required by the government and company policy.
**Minimum Requirements:**
+ Bachelor of Science degree in related field
+ 5+ years of experience in analysis and modeling of modern combat aircraft and other airborne systems
+ Collecting and establishing the pedigree of input data, conducting risk analysis; model manipulation and modification
**Preferred Requirements:**
+ Experience with AFSIM or Brawler Air Combat Simulation
+ Experience in Air Combat (preferably Air-to-Air), fighter aircraft weapons systems, and weapons employment
+ Experience developing study plans that include background, purpose of study, scope/limitations, critical assumptions and constraints, measures of effectiveness, study parameters and variables, methodology description, data requirements and schedule
+ Experience in programming in C/C++, Fortran, R, Python, MATLAB, and SQL and using Microsoft Office products
**Clearance Requirements:**
+ US Citizenship required and an active Secret security clearance with the ability to obtain and maintain a Top-Secret clearance with Sensitive Compartmented Information (TS/SCI) eligibility
**Physical Requirements:**
+ Must be able to remain in a stationary position 50%
+ Constantly operates a computer and other office productivity machinery, such as a calculator, copy machine and computer printer
ManTech International Corporation, as well as its subsidiaries proactively fulfills its role as an equal opportunity employer. We do not discriminate against any employee or applicant for employment. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.
If you are a qualified individual with a disability and require a reasonable accommodation to apply for a position with ManTech through its online applicant system, please email us at and provide your name and contact information.

**Req ID:** RQ200244
**Type of Requisition:** Regular
**Clearance Level Must Be Able to Obtain:** None
**Public Trust/Other Required:** NACI (T1)
**Job Family:** Research
**Skills:**
Clinical Study Protocols,Research Activities,Research Protocols
**Experience:**
2 + years of related experience
**US Citizenship Required:**
Yes
**Job Description:**
GDIT's Military Health team is seeking a Clinical Research Coordinator (CRC) to support the Combat Trauma Research Group (CTRG) and Clinical Investigations Department (CID) at the Naval Medical Center Portsmouth (NMCP).
The CRC is responsible for providing research coordination support for IRB- and IACUC -approved human and animal research protocols in conjunction with the CTRG investigators.
HOW YOU WILL MAKE AN IMPACT:
+ Work is performed in ambulatory care spaces, inpatient wards, and the animal vivarium, all of which present some risk of exposure to infectious disease, for which gloves, masks, or gowns provided by the government entity may be required for safety reasons.
+ Coordinate research activities of assigned IRB and IACUC-approved study protocols, such as IRB pediatric and adult studies or IACUC animal studies.
+ Supports the Department Head of CID and is accountable for research related matters to the PIs of each research protocol. Provide support to the Department Head of CID and the PI of each protocol in accordance with written policies and procedures as set forth in Title 21 of the Code of Federal Regulations, NMCP and Bureau of Medicine & Surgery (BUMED) instructions.
+ Ensure all studies performed are in accordance with the approved protocol and applicable local, state, and federal regulations.
+ Work closely with the Senior Research Technician/Supply Purchase officer in identifying the study materials, equipment and/or research animals needed in the research protocol and in accordance with CID IACUC policies and animal facility standard operating procedures.
+ Coordinate with the PI to ensure all resources, including supplies, are available as necessary to meet research timelines.
+ Ensure effective communication with patients, their families and/or significant others, providers, clinical staff, clerical staff, and collaborative institutions.
+ Report data on research studies in accordance with IRB/IACUC-approved protocols and applicable regulations with final government approval.
+ Assist with recruiting and screening patients using protocol inclusion/exclusion criteria and refer eligible patients to the PI for final evaluation.
+ Assist Government personnel with ensuring the consent process has taken place effectively and all questions are answered satisfactorily and documented.
+ Assist with providing education to patients on compliance, possible side effects, drug interactions and the importance of contacting the coordinator.
+ Assist with coordinating the performance of phlebotomies, electrocardiograms, initiate intravenous infusions, vital signs, specimen collection and other procedures as required by the protocol.
+ Maintain proficiency required to coordinate clinical research such as: communication skills and leadership skills as the coordinator of complex human and animal research protocols.
+ Maintain proficiency in appointment booking, and coordinating laboratory studies, x-rays, and other tests.
+ Assist with assigning appropriate randomization number, per protocol design, to subjects.
+ Assist the Research Pharmacist with ensuring that drugs are correctly dispensed as per protocol.
+ Assist with maintaining accurate documentation record of drugs received.
+ Assist with processing and preparing specimens for lab analysis and shipping.
+ Observe universal precautions and OSHA standards when processing or handling specimens.
+ Collect laboratory results and consult with the PI for follow-up care.
+ Ensure collection of data in a timely and accurate manner and submit information to coordinating centers as required, subject to final Government approval.
+ Ensure reporting of adverse events to the governing agencies (IRB/IACUC) and sponsors as required by protocol and regulations.
+ Ensure in the research study is in with regulations and standard operating procedures, to include complete documentation of status and progress.
+ Assist with maintaining detailed documentation of the research study as required by the protocol and the PI's File Binder/Regulatory Binder.
+ Assist with preparing reports and other correspondence regarding the research protocol for IACUC, granting agencies, industry sponsors and other organizations as required by regulation and/or the protocol, subject to final Government approval.
+ Assist with producing protocol amendments and continuing reviews in the eIRB system, subject to final Government approval.
+ Submit deviation study reports to the IACUC/IRB, subject to final Government approval.
+ Attend conferences and other meetings as required by the protocol, the PI or sponsoring agency. Subcontractor personnel shall not function as voting members.
**WHAT YOU'LL NEED TO SUCCEED:**
+ Bachelor's degree.
+ 3+ years of clinical research/ clinical investigations experience.
+ Experience coordinating research activities following IRB.
+ US citizenship with ability to pass a public trust clearance.
? **GDIT IS YOUR PLACE:**
+ 401K with company match
+ Comprehensive health and wellness packages
+ Internal mobility team dedicated to helping you own your career
+ Professional growth opportunities including paid education and certifications
+ Cutting-edge technology you can learn from
+ Rest and recharge with paid vacation and holidays
#GDITFedHealthJobs
#GDITHealth
#MilitaryHealthGDITJobs
#GDITpriority
The likely salary range for this position is $62,962 - $73,025. This is not, however, a guarantee of compensation or salary. Rather, salary will be set based on experience, geographic location and possibly contractual requirements and could fall outside of this range.
Our benefits package for all US-based employees includes a variety of medical plan options, some with Health Savings Accounts, dental plan options, a vision plan, and a 401(k) plan offering the ability to contribute both pre and post-tax dollars up to the IRS annual limits and receive a company match. To encourage work/life balance, GDIT offers employees full flex work weeks where possible and a variety of paid time off plans, including vacation, sick and personal time, holidays, paid parental, military, bereavement and jury duty leave. To ensure our employees are able to protect their income, other offerings such as short and long-term disability benefits, life, accidental death and dismemberment, personal accident, critical illness and business travel and accident insurance are provided or available. We regularly review our Total Rewards package to ensure our offerings are competitive and reflect what our employees have told us they value most.
We are GDIT. A global technology and professional services company that delivers consulting, technology and mission services to every major agency across the U.S. government, defense and intelligence community. Our 30,000 experts extract the power of technology to create immediate value and deliver solutions at the edge of innovation. We operate across 50 countries worldwide, offering leading capabilities in digital modernization, AI/ML, Cloud, Cyber and application development. Together with our clients, we strive to create a safer, smarter world by harnessing the power of deep expertise and advanced technology.
Join our Talent Community to stay up to date on our career opportunities and events at Opportunity Employer / Individuals with Disabilities / Protected Veterans

ASRC Federal is a leading government contractor furthering missions in space, public health and defense. As an Alaska Native owned corporation, our work helps secure an enduring future for our shareholders. Join our team and discover why we are a top veteran employer ( and Certified Great Place to Work ( Federal is seeking an **Operations Research Analyst** for anticipated openings in 2025. **This is a pipeline requisition to collect resumes in preparation of future hiring** . We proudly support the US Coast Guard BOD ALC (Aviation Logistics Center) and their mission of keeping aircraft maintained and serviced so those serving in the Coast Guard can keep our country safe. The Aviation Logistics Center's mission includes Depot Level Maintenance, Engineering, Supply, Procurement and Information Services. ASRC Federal offers an excellent salary and benefits package that includes certification reimbursement and a matching 401k with immediate vesting. We foster a climate of professional development and recognition for excellence. Find out why we were certified consistently as a "Great Place to Work".
Requirements:
+ US Citizenship is Required with ability to pass a federal government background investigation.
+ BA/BS in Operations Research, Industrial Engineering, Business, Engineering, Information Systems Management or Mathematics AND four (4) years of operations research or related experience. For non-related degrees, six (6) years of experience is required. For an AA/AS degree, eight (8) years is required.
+ Experience with formulating and applying mathematical modeling or other optimizing methods to develop and interpret information that assists with decision making, policy formulations and other functions.
+ Experience in a maintenance depot is preferred; aircraft/helicopter is a plus.
+ Experience in determining mission supports costs to include maintenance, repair, sparing, warehousing, labor hours, transportation and other relevant drivers.
+ Excellent interpersonal and communication skills required.
+ Experience with tools such as SAS, R or Python (or similar tools) is a plus.
Responsibilities:
+ Formulate and apply mathematical modeling to develop and interpret information for decision making purposes.
+ Develop business case analysis with stated forecasting variables in order to provide different courses of actions for mission support and sustainment decisions.
+ Utilize software tools for improving current models and forecasts.
+ Establish project timelines, monitor work completion and utilize effective communication.
We invest in the lives of our employees, both in and out of the workplace, by providing competitive pay and benefits packages. Benefits offered may include health care, dental, vision, life insurance; 401(k); education assistance; paid time off including PTO, holidays, and any other paid leave required by law.
**_EEO Statement_**
_ASRC Federal and its Subsidiaries are Equal Opportunity employers. All qualified applicants will receive consideration for employment without regard to race, gender, color, age, sexual orientation, gender identification, national origin, religion, marital status, ancestry, citizenship, disability, protected veteran status, or any other factor prohibited by applicable law._
**Job Details**
**Job Family** **Supply Chain**
**Job Function** **Logistics**
**Pay Type** **Salary**

**Description**
PCSI is looking for Gardener at NASA Langley Research Center. The Gardner will assist in the accomplishment of minor grounds maintenance tasks and maintain the health and appearance of plants by watering, weeding, and fertilizing. This position will report to the Director of Operations and is based in Hampton, Virginia. **Typical work hours will be 7am-3:30pm Monday-Friday.**
**Benefits Include:**
+ Base pay is $19.79/hr.
+ 21 days of PTO per year, in addition to all federal holidays.
+ Medical, dental, vision, and other coverage: employer contribution offered to cover employee-only tier.
**Who We Are:**
PCSI is a non-profit organization whose mission is to enhance the lives of people with disabilities through employment, advocacy, and partnerships. We vet, prepare, lead, and sustain a skilled workforce that provides top-tier services at job sites across the country. Our areas of expertise are wide and diverse; total facilities maintenance, hospital environmental services, custodial and grounds, disability awareness training, job coaching, and job placement are just a few. We integrate people with disabilities and veterans into meaningful jobs with competitive wages and benefits. Serving people of all abilities in their life's journey is at the heart of what we do.
**What You'll Do as Gardner:**
+ Assist in the accomplishment of minor grounds maintenance tasks.
+ Maintain the health and appearance of plants by watering, weeding, and fertilizing.
+ Use equipment to maintain grounds, such as mowing lawns, edging grass, and trimming trees.
+ Keep grounds clear of debris and litter.
+ Perform preventive maintenance and cleaning of grounds equipment.
+ Follow safety and health regulations for landscaping and meet standards of the contract
**Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.**
**What You'll Need:**
+ High school diploma or GED equivalent required.
+ Experience and/or formal vocational and/or technical training in grounds maintenance preferred
**Knowledge, Skills and Abilities:**
+ Ability to use hand tools, power tools, and appliances used in landscaping.
+ Familiarity with regional plant life, local pests, and synthetic and natural fertilizers.
+ Demonstrated accuracy and speed in work.
+ Good written and verbal communication skills.
+ Self-starter with the ability to work both with minimal supervision and as a team player.
+ Must have the ability to effectively read, write, and speak the English language.
**Other Requirements:**
+ Ability to pass criminal, and drug screenings.
+ Ability to pass driving screenings preferred.
+ Ability to work outside in inclement weather and be exposed to various dirt, debris, and odors.
+ Ability to move about the facilities approximately 90% of the time during working hours.
+ Ability to work any daytime hours or day of the week, including weekends and holidays.
+ Preferred to possess valid driver's license and maintain good driving record.
+ If required, ability to obtain and maintain security clearance and base access to assigned site(s).
Please note that this job description is not designed to cover or contain a comprehensive listing of activities, duties, or responsibilities that are required of the employee for this job. Duties, responsibilities, and activities may change at any time with or without notice.
**All veterans and/or persons with all types of disabilities are strongly encouraged to apply!**
Equal Opportunity Employer/Protected Veterans/Individuals with Disabilities
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights ( notice from the Department of Labor.