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AC
Veterinary Assistant
A Caring Doctor (Minnesota), P.A.
Banfield Overland Park, KS
- $16.47 to $21.05 USD / hour
If you are a current associate, you will need to apply through our internal career site. Please log into Workday and click on the Jobs Hub app or search for Browse Jobs.
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AC
Veterinary Assistant
A Caring Doctor (North Carolina), P.C.
Banfield Northlake Mall, NC
- $15.65 to $20 USD / hour
If you are a current associate, you will need to apply through our internal career site. Please log into Workday and click on the Jobs Hub app or search for Browse Jobs.
Added just now
MM
Veterinary Assistant
Medical Management International, Inc.
Banfield Kildeer, IL
- $18.12 to $23.15 USD / hour
If you are a current associate, you will need to apply through our internal career site. Please log into Workday and click on the Jobs Hub app or search for Browse Jobs.
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AC
Practice Manager - Cornelius
A Caring Doctor (North Carolina), P.C.
Banfield Cornelius, NC
- $62,450 to $90,205 USD / year
…etc.), including direct supervisory experience (includes hiring, associate development,…
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Clinical Director – Adolescent Behavioral Health, Fallbrook
A BETTER LIFE RECOVERY LLC
Bonsall, CA
Minimum Licensure/Education – Associate licensed clinician (AMFT, ACSW, APCC) with experience in a mental health treatment environment. Managerial experience. Master’s degree from an…
Added 3 mins ago
F-22 Flight Test Instrumentation Engineer (Associate or Experienced)
The Boeing Company
Edwards AFB, CA
…warfighting capabilities of the Air Force through system integration, development, test and evaluation of the F-22…
Added 3 mins ago
Procurement Financial Analyst (Associate, Experienced or Senior)
Boeing
Hazelwood, MO
We are seeking talented Procurement Financial Analysts (Associate, Experienced or Senior) to join Boeing’s Defense Procurement Financial Analysis team in Hazelwood, MO.
Added 3 mins ago
Associate Software Engineer
The Boeing Company
Albuquerque, NM · El Segundo, CA
The Boeing Company has an exciting opportunity for an Associate Software Engineer, Front End Developer to support the Space Mission Systems (SMS) Rapid Space Capabilities (RSC) portfolio,…
Added 5 mins ago
(INTERNAL ONLY) Social Worker I, II - HFW Facilitator (Bilingual Preferred)
The Family Care Network Inc.
San Luis Obispo, CA
…provide therapeutic interventions and functional life skill development in various settings, including homes, schools, and the community. The Social Worker may serve as the team…
Added 6 mins ago
Benefits Strategy Manager
Ascension
Remote, United States
Use focus groups, survey data, and associate feedback to identify gaps, refine offerings, and elevate employee satisfaction metrics.
Added 6 mins ago
CT Tech
Ascension
Evansville, IN
High School diploma equivalency with 2 years of cumulative experience OR Associate's degree/Technical degree OR 4 years of applicable cumulative job specific experience required.
Added 6 mins ago
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Ascension
Evansville, IN
High School diploma equivalency with 3 years of cumulative experience OR Associate's degree/Technical degree with 2 years of experience OR 7 years of applicable cumulative job specific…
Added 6 mins ago
Patient Care Technician Orthopedics
Ascension
Newburgh, IN
Career growth: Ascension-paid tuition (Vocare), reimbursement, ongoing professional development and online learning
Added 6 mins ago
Patient Care Technician Orthopedics PreOp/PACU
Ascension
Newburgh, IN
Career growth: Ascension-paid tuition (Vocare), reimbursement, ongoing professional development and online learning
Added 6 mins ago
Registered Nurse Clinic NE
Ascension
Remote, United States
…Valid state license required specific to the state in which the associate…
Added 6 mins ago
Patient Transporter
Ascension
Evansville, IN
Career growth: Ascension-paid tuition (Vocare), reimbursement, ongoing professional development and online learning
Added 6 mins ago
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Ascension
Remote, United States
CX Research & Program Management: Oversee day-to-day consumer experience research, continuous listening programs, and cross-functional data integration.
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Ascension
Pensacola, FL
Career growth: Ascension-paid tuition (Vocare), reimbursement, ongoing professional development and online learning
Added 6 mins ago
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Ascension
Evansville, IN
Career growth: Ascension-paid tuition (Vocare), reimbursement, ongoing professional development and online learning
Added 6 mins ago
Medicare Wellness RN
Ascension
Evansville, IN
Career growth: Ascension-paid tuition (Vocare), reimbursement, ongoing professional development and online learning
Added 6 mins ago
Program Manager
Ascension
Remote, United States
Collaborates with CX Onsite Team leaders to identify program opportunities.
Added 6 mins ago
Ambulatory Risk Manager
Ascension
Remote, United States
Assists with the development and implementation of initiatives and policies and procedures, including associate and Physician/APP education activities, Provider Associate Care Team (PACT)…
Added 6 mins ago
Nursing Assistant Certified Long Term Care
Ascension
Wichita, KS
Career growth: Ascension-paid tuition (Vocare), reimbursement, ongoing professional development and online learning
Added 6 mins ago
Nursing Assistant Certified Long Term Care
Ascension
Wichita, KS
Career growth: Ascension-paid tuition (Vocare), reimbursement, ongoing professional development and online learning
Added 6 mins ago
Emergency Dispatch Operator
Ascension
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Career growth: Ascension-paid tuition (Vocare), reimbursement, ongoing professional development and online learning

Global Solutions Network Inc

Senior Research Associate (Clinical) - NIH

Bethesda, MD, United States

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Job details

Posting language: English
Posted: Oct 30, 2026

Original job description

Global Solutions Network (GSN), a federal government contracting firm, presents this full time, long-term position supporting GSN's customer at the National Institutes of Health (NIH). This position provides a competitive salary and comprehensive benefits.

If interested, please provide an up-to-date resume.

Responsibilities.

Assist researchers develop, prepare internal research proposals, abstract submissions, poster presentations and manuscript drafts.
Assist researchers develop protocol documentation including schemas, patient calendars and teaching aids.
Assist researchers develop clinical research informed consent and other ethics and regulatory related documentation.
Assist researchers collect, organize and maintain all study documentation to include investigator qualifications, trial logs, and safety reports.
Assist researchers maintain accurate records of all protocols and study applications, safety reports, annual reports and correspondence.
Assist researchers write and edit study protocols, and prepare amendments, reviews, reports, and other necessary forms.
Maintain data files within multiple software systems, including computerized procurement reports and communication programs.
Perform entry and cleanup of study of the questionnaire data in various databases, and conduct queries to answer researcher questions.
Assist researchers track study requests and protocol approvals, maintaining a record of all submissions and status of approvals.
Assist IRB administrator collect, review and maintain all IRB records.
Assist researchers review and submit protocol actions for clearance within the NIH Protocol Tracking and Management System.
Organize quality assurance activities with pertinent regulatory bodies such as the Food and Drug Administration (FDA), NIH, pharmaceuticals and others.
Assist researchers prepare and communicate with IRB and NIH Clinical Center for protocol approval.
Assist staff on onsite and offsite patient scheduling issues and processes, form preparation, etc.
Assist researchers coordinate recruitment, scheduling, travel and admission of research study participants with clinical staff.
Assist researchers screen study participants and document results of screenings.
Develop internal research proposals, abstract submissions, poster presentations and manuscript drafts.
Develop protocol documentation including schemas, patient calendars and teaching aids.
Develop clinical research informed consent and other ethics and regulatory related documentation.
Develop standard operating procedures (SOPs) for the clinical study.
Prepare study reports and status updates, including amendments, audits and other administrative documentation.
Prepare IND and IDE safety, clinical study reports and other regulatory correspondences, including initial submissions, information requests, amendments, and annual reports.
Collect, organize and maintain all study documentation to include investigator qualifications, trial logs, and safety reports.
Maintain accurate records of all protocols and study applications, safety reports, annual reports and correspondence.
Write and edit study protocols, and amendments, reviews, reports, and other necessary forms.
Coordinate with IRB administrator to collect, review and maintain all IRB records.
Review and submit protocol actions for clearance within the NIH Protocol Tracking and Management System.
Develop new and review completed protocol documentation including schemas, patient calendars and teaching aids.
Coordinate with IRB administrator to collect, review and maintain all IRB records.
Develop and submit protocol actions for clearance within the NIH Protocol Tracking and Management System.
Conduct quality assurance activities in preparation for regulatory audits by FDA, NIH, pharmaceuticals and others.
Communicate with IRB and NIH Clinical Center for protocol approval.
Prepare and submit documentation for regulatory bodies in support of clinical trials.
Review completed internal research proposals, abstract submissions, poster presentations and manuscript drafts and recommend changes.
Maintain all study documentation to include investigator qualifications, trial logs, and safety reports and review for accuracy and completeness.
Review records of all protocols and study applications, safety reports, annual reports and correspondence for accuracy and completeness.
Review study protocols, and amendments, reviews, reports, and other necessary forms for accuracy and completeness.
Maintain all regulatory trial documentation including maintaining a complete and up-to-date Regulatory Binder for each trial, documentation of investigator qualifications, trial logs and safety reports and review for accuracy and completeness.
Coordinate with IRB administrator to collect, review and maintain all IRB records.
Conduct quality assurance activities in preparation for regulatory audits by FDA, NIH, pharmaceuticals and others.
Communicate with IRB and NIH Clinical Center for protocol approval.
Coordinate education and guidance regarding research activities, procedures and standards for new staff members.
Maintain documentation of clinical research training of staff.
Educate research staff regarding relevant aspects of regulatory process including requirements of protocol development, conduct of research trials, regulatory change, IRB and FDA submission requirements, radiation safety requirements, ethics clearances, and technology transfer.
Educate and train investigators in new protocol management systems; maintain a smooth flow in process for IRB submissions.
Meet with investigators and advise them of the documentation and approvals they will need to initiate a clinical study based on the type, location and complexity of the proposal.

Qualifications.

Master's degree in a related field.
CITI certification
Familiarity with Electronic Data Capture Systems
Demonstrated experience with:
Liaising with regulatory authorities
Training clinical trial site staff
Coordinating project meetings
Previous clinical trial work

Benefits.

Medical, Dental, & Vision Coverage
Paid Time Off and Paid Holidays
401K/Profit Sharing Plan
Flexible Spending Accounts (Healthcare & Dependent Care)
Pretax Parking & Transportation Plan
Short-Term & Long-Term Disability Insurance
Life & AD&D Insurance
Professional Development/Education
Employee Referral Bonuses
Employee Discount Program
Merit Bonuses
Employee Assistance Program
Travel Assistance Program

Global Solutions Network, Inc. (GSN) is an Equal Employment Opportunity (EEO) employer. It is the policy of the GSN to provide equal employment opportunities to all qualified applicants without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected US veteran or disabled status, or genetic information.

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More about this job

Skills

Research
Presentation skills
Documentation
Teaching
Clinical research
Procurement
Communication skills
Quality assurance
Scheduling
IDE
Clinical trials

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