Kennedy Krieger Institute Visa Sponsorship Jobs USA
Kennedy Krieger Institute is a nationally recognized leader in pediatric rehabilitation and developmental disabilities research. For healthcare and research professionals who need visa sponsorship, Kennedy Krieger has a strong track record across multiple visa categories, making it a compelling target for international job seekers in clinical and scientific roles.
Find Kennedy Krieger Institute JobsOverview
Showing 5 of 60+ Kennedy Krieger Institute Visa Sponsorship Jobs USA
See all 60+ Kennedy Krieger Institute Visa Sponsorship Jobs USA
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Kennedy Krieger Institute Visa Sponsorship Jobs USA.
Get Access To All JobsINTRODUCTION
The Senior Research Coordinator in the Clinical Trials Unit will be primarily responsible for complex project management for multiple research studies related to psychiatric conditions in pediatric patients. Activities include but are not limited to project execution, implementation, daily administration and close out for multiple research studies. The Senior Research Coordinator will ensure precise implementation of and adherence to study protocol, create all study documentation, oversee operating procedures, timelines, IRB applications, data preparation, and other research-related activities. In addition to operational management of multiple research studies, the Senior Research Coordinator will see patients participating in ongoing clinical trials, and will be responsible for specimen collection, processing, and DOT/ IATA compliant handling and shipment.
ROLE AND RESPONSIBILITIES
- Prepare and submit Institutional Review Board (IRB) required materials, as well as prepare compliance and regulatory documentation for local, state, and federal agencies and any other pertinent entity.
- Manage ongoing IRB activities including preparation and submission of initial applications, changes in research, protocol deviations, annual continuing reviews, and termination reports.
- Create and maintain multiple IRB accounts and investigator notebooks and report adverse events.
- Implement and ensure adherence to protocol for multiple studies simultaneously.
- Respond to questions regarding protocol content from site staff.
- Continuously educate and train personnel, patients, and caregivers on protocol compliance.
- Identify protocol problems, inform investigators, and assist in problem resolution efforts.
- Develop protocol compliant site-specific study documentation for multiple studies. Responsible for developing and producing custom and routine reports as necessary.
- Conduct ongoing clinical trial and research study activities with minimal direction. Such activities include:
1. participant recruitment and scheduling
2. study procedure scheduling and coordination
3. conducting patient visits and executing study procedures
4. managing specimen collection and processing
5. obtaining results and ensuring clinician review
6. documentation completion
7. reporting
- Administer blood draws via venipuncture, ECGs, and collect vital signs for pediatric patients. Process and ship collected biomaterials in accordance with DOT and IATA hazmat regulations.
- Responsible for independent project management of multiple research studies and regular communication with research collaborators, study sponsor, and study vendors.
- Manage research data in accordance with protocols established by sponsors and the Institute. Lead efforts on data preparation, data entry, transfer, archiving, maintenance, and analysis as needed. Provide and communicate data-related study matters to research collaborators.
- Oversee deliverables for monitoring requirements, site initiation visits, review and approval of monitoring plan; ensure monitoring is conducted in accordance with Standard Operating Procedures (SOPs) and monitoring plan; ensure timeliness of monitoring and follow-up action items are completed.
- Responsible for resolving all study-related queries, final study closeout, and lock of databases.
- Attend study and research-related meetings, conferences, and teleconferences.
- Develop and maintain SOPs, for the program and the Institute, that adhere to and promote to the tenets of Good Clinical Practice.
- Participate in research planning, development, and legacy activities.
- Assist with general administrative work, including processing subject reimbursements and incentives, inventory and ordering supplies, and organizing service billing.
BASIC QUALIFICATIONS
- Bachelor’s degree is required, preferably in psychology, statistics, or neurosciences.
- Master’s degree preferred.
PREFERRED QUALIFICATIONS
Requires at least four (4) years of research related work experience.
COMPENSATION
- USD $50,786.11/Yr.
- USD $87,503.31/Yr.
INTRODUCTION
The Senior Research Coordinator in the Clinical Trials Unit will be primarily responsible for complex project management for multiple research studies related to psychiatric conditions in pediatric patients. Activities include but are not limited to project execution, implementation, daily administration and close out for multiple research studies. The Senior Research Coordinator will ensure precise implementation of and adherence to study protocol, create all study documentation, oversee operating procedures, timelines, IRB applications, data preparation, and other research-related activities. In addition to operational management of multiple research studies, the Senior Research Coordinator will see patients participating in ongoing clinical trials, and will be responsible for specimen collection, processing, and DOT/ IATA compliant handling and shipment.
ROLE AND RESPONSIBILITIES
- Prepare and submit Institutional Review Board (IRB) required materials, as well as prepare compliance and regulatory documentation for local, state, and federal agencies and any other pertinent entity.
- Manage ongoing IRB activities including preparation and submission of initial applications, changes in research, protocol deviations, annual continuing reviews, and termination reports.
- Create and maintain multiple IRB accounts and investigator notebooks and report adverse events.
- Implement and ensure adherence to protocol for multiple studies simultaneously.
- Respond to questions regarding protocol content from site staff.
- Continuously educate and train personnel, patients, and caregivers on protocol compliance.
- Identify protocol problems, inform investigators, and assist in problem resolution efforts.
- Develop protocol compliant site-specific study documentation for multiple studies. Responsible for developing and producing custom and routine reports as necessary.
- Conduct ongoing clinical trial and research study activities with minimal direction. Such activities include:
1. participant recruitment and scheduling
2. study procedure scheduling and coordination
3. conducting patient visits and executing study procedures
4. managing specimen collection and processing
5. obtaining results and ensuring clinician review
6. documentation completion
7. reporting
- Administer blood draws via venipuncture, ECGs, and collect vital signs for pediatric patients. Process and ship collected biomaterials in accordance with DOT and IATA hazmat regulations.
- Responsible for independent project management of multiple research studies and regular communication with research collaborators, study sponsor, and study vendors.
- Manage research data in accordance with protocols established by sponsors and the Institute. Lead efforts on data preparation, data entry, transfer, archiving, maintenance, and analysis as needed. Provide and communicate data-related study matters to research collaborators.
- Oversee deliverables for monitoring requirements, site initiation visits, review and approval of monitoring plan; ensure monitoring is conducted in accordance with Standard Operating Procedures (SOPs) and monitoring plan; ensure timeliness of monitoring and follow-up action items are completed.
- Responsible for resolving all study-related queries, final study closeout, and lock of databases.
- Attend study and research-related meetings, conferences, and teleconferences.
- Develop and maintain SOPs, for the program and the Institute, that adhere to and promote to the tenets of Good Clinical Practice.
- Participate in research planning, development, and legacy activities.
- Assist with general administrative work, including processing subject reimbursements and incentives, inventory and ordering supplies, and organizing service billing.
BASIC QUALIFICATIONS
- Bachelor’s degree is required, preferably in psychology, statistics, or neurosciences.
- Master’s degree preferred.
PREFERRED QUALIFICATIONS
Requires at least four (4) years of research related work experience.
COMPENSATION
- USD $50,786.11/Yr.
- USD $87,503.31/Yr.
Job Roles at Kennedy Krieger Institute
See all 60+ Kennedy Krieger Institute Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Kennedy Krieger Institute roles.
Get Access To All JobsTips for Finding Kennedy Krieger Institute Visa Sponsorship Jobs USA
Target clinical and research roles first
Kennedy Krieger's sponsorship activity is concentrated in healthcare and research positions. Focus your applications on clinical, scientific, and therapy roles where the institute has the strongest hiring history and the most established sponsorship pathways.
Understand which visa types they support
Kennedy Krieger sponsors H-1B, TN, J-1, and F-1 OPT and CPT visas, plus Green Card pathways. Knowing which category fits your background before you apply helps you frame your eligibility clearly and speeds up early sponsorship conversations with HR.
Engage early if you're on OPT
If you're on F-1 OPT, reach out to Kennedy Krieger's HR team early. Healthcare institutions with active sponsorship programs often plan H-1B transitions well in advance of cap deadlines, and early conversations protect your work authorization timeline.
Leverage the Green Card pathway signal
Kennedy Krieger has sponsored Green Cards alongside H-1B visas, signaling long-term hiring intent. If permanent residency is your goal, this is a strong indicator the institute may support EB-2 or EB-3 sponsorship for the right candidate.
Research open roles before reaching out
Before contacting the institute's HR team, identify specific open positions that match your credentials. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history and apply to Kennedy Krieger roles with confidence you're not wasting your time.
Align your credentials with specialty occupation standards
H-1B eligibility at a healthcare institution like Kennedy Krieger requires your role to qualify as a specialty occupation. Clinical, therapy, and research positions typically meet this standard. Make sure your degree field directly matches the job's requirements before applying.
Frequently Asked Questions
Does Kennedy Krieger Institute sponsor H-1B visas?
Yes, Kennedy Krieger Institute sponsors H-1B visas and is among the more active sponsors in the pediatric healthcare and research sector. Sponsorship is concentrated in clinical, scientific, and specialized therapy roles where a degree in a specific field is required. If you're targeting H-1B sponsorship, aligning your application to roles with clear specialty occupation credentials gives you the strongest shot.
What visa types does Kennedy Krieger Institute sponsor?
Kennedy Krieger Institute sponsors a range of visa categories including H-1B, TN visa, J-1 visa, and F-1 OPT and CPT for students and early-career professionals. The institute also has a track record of supporting Green Card sponsorship through EB-2 and EB-3 pathways, making it a strong option for candidates seeking long-term work authorization in the United States.
Which roles at Kennedy Krieger Institute are most likely to receive visa sponsorship?
Sponsorship at Kennedy Krieger is most common in clinical and research-facing positions, including roles in psychology, physical and occupational therapy, behavioral health, neurology, and biomedical research. These positions typically require specialized degrees that meet H-1B specialty occupation standards. Administrative and general support roles are less frequently sponsored, so candidates should focus on credentialed clinical or scientific positions.
How do I find open visa-sponsored jobs at Kennedy Krieger Institute?
Migrate Mate is the most efficient way to find sponsored roles at Kennedy Krieger Institute. Unlike general job boards, Migrate Mate filters by verified sponsorship history so you can browse Kennedy Krieger openings knowing the employer has a real track record. Search by visa type, role, or location to narrow down positions that match your background and immigration needs.
How do I approach the application process at Kennedy Krieger Institute as an international candidate?
Start by identifying a role where your degree and experience align closely with the job requirements, since Kennedy Krieger evaluates sponsorship on a role-by-role basis. Apply through the institute's official careers portal, and be transparent about your visa status in early conversations. If you're on OPT, flag your H-1B cap deadline to HR as early as possible so there's adequate lead time to prepare your petition before the April filing window.