E-3 Visa Research Coordinator Jobs
Research Coordinator roles in the U.S. qualify for E-3 visa sponsorship when the position requires a bachelor's degree in a relevant field such as public health, social sciences, or life sciences. The E-3 has no lottery and no annual cap, making it one of the most practical paths for Australian professionals pursuing U.S.-based research careers.
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Do you want to help Stanford University better understand and measure the effects of neuromuscular disorders, including: muscular dystrophies, spinal muscular atrophy, amyotrophic lateral sclerosis, inherited neuropathies, and other conditions?
If you…
- Enjoy working directly with patients and their families
- Are excited to work with patients affected by neuromuscular disorders
- Are exceptionally organized and can balance multiple projects at one time
- Have excellent time management and can meet deadlines
- Can work independently
- Are a proven quick learner
Then we offer…
- The opportunity to work in a collaborative team of neuromuscular investigators
- The chance to contribute to understanding and treatment of previously fatal neuromuscular disorders
- Exciting and positive environment where you will always learn new things
- Teamwork and camaraderie
- Competitive full-time salary
- Excellent Stanford benefits
The Neuromuscular Division of Neurology is seeking a Clinical Research Coordinator Associate (CRCA) to coordinate the oversight and implementation of research protocols assuring efficiency and regulatory compliance. The CRCA will be responsible for running a subset of the neuromuscular division’s investigator-initiated trials and a few industry-sponsored drug trials. These may include gene therapies, small molecule drug trials, and other projects dealing with pediatric and adult neuromuscular conditions including ALS, spinal muscular atrophy, Duchenne muscular dystrophy, myotonic dystrophy, myasthenia gravis, and others. There are opportunities for long term growth within the team, or the position can be a launching pad for careers in biomedical science. These studies of devastating nerve and muscle disorders will be conducted at the Stanford University Medical Center. Interested candidates should include a CV and Cover Letter addressing how your education and experience relates to the position as described above.
Duties include:
- Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out.
- Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.
- Coordinate collection of study specimens and processing.
- Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
- Ensure compliance with research protocols and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed.
- Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
- Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
- Independently performs exercise testing and outcome evaluations for patients.
- Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
- Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
- Participate in monitor visits and regulatory audits.
- Other duties may also be assigned
DESIRED QUALIFICATIONS:
- Experience with database, data management, FDA regulations, IRB requirements and the Stanford clinical research environment highly desirable.
- Ability to work both independently and as part of a multidisciplinary team
- Ability to determine workload priorities in an appropriate way to accomplish tasks and goals, meet deadlines and anticipate and solve potential problems
- Experience with patients or research subjects
- Strong general computer skills and ability to quickly learn and master computer programs.
- Good oral and written communication skills to effectively work with physicians, clinical staff and other health care professionals.
- Proficiency with Microsoft Office, Word, Excel and various industry-oriented electronic data capture programs
- Excellent organizational skills and attention to detail in maintaining accurate, retrievable records
EDUCATION & EXPERIENCE (REQUIRED):
Two year college degree and two years related work experience or a Bachelor’s degree in a related field or an equivalent combination of related education and relevant experience.
KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):
- Strong interpersonal skills.
- Proficiency with Microsoft Office.
- Knowledge of medical terminology.
- Computational Skills
CERTIFICATIONS & LICENSES:
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
Physical Requirements:
- Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
- Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
- Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.
- Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.
WORK STANDARDS:
- Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
- Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
- Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, http://adminguide.stanford.edu.
The expected pay range for this position is $34.56 to $40.30 per hour.
Stanford University provides pay ranges representing its good faith estimate of the salary or hourly wage the university reasonably expects to pay for a position upon hire. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location, and external market pay for comparable jobs.
At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website provides detailed information on Stanford's extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process.
Consistent with its obligations under the law, the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring a reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources by submitting a contact form.
Stanford is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.
The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned.

Do you want to help Stanford University better understand and measure the effects of neuromuscular disorders, including: muscular dystrophies, spinal muscular atrophy, amyotrophic lateral sclerosis, inherited neuropathies, and other conditions?
If you…
- Enjoy working directly with patients and their families
- Are excited to work with patients affected by neuromuscular disorders
- Are exceptionally organized and can balance multiple projects at one time
- Have excellent time management and can meet deadlines
- Can work independently
- Are a proven quick learner
Then we offer…
- The opportunity to work in a collaborative team of neuromuscular investigators
- The chance to contribute to understanding and treatment of previously fatal neuromuscular disorders
- Exciting and positive environment where you will always learn new things
- Teamwork and camaraderie
- Competitive full-time salary
- Excellent Stanford benefits
The Neuromuscular Division of Neurology is seeking a Clinical Research Coordinator Associate (CRCA) to coordinate the oversight and implementation of research protocols assuring efficiency and regulatory compliance. The CRCA will be responsible for running a subset of the neuromuscular division’s investigator-initiated trials and a few industry-sponsored drug trials. These may include gene therapies, small molecule drug trials, and other projects dealing with pediatric and adult neuromuscular conditions including ALS, spinal muscular atrophy, Duchenne muscular dystrophy, myotonic dystrophy, myasthenia gravis, and others. There are opportunities for long term growth within the team, or the position can be a launching pad for careers in biomedical science. These studies of devastating nerve and muscle disorders will be conducted at the Stanford University Medical Center. Interested candidates should include a CV and Cover Letter addressing how your education and experience relates to the position as described above.
Duties include:
- Serve as primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from startup through close-out.
- Determine eligibility of and gather consent from study participants according to protocol. Assist in developing recruitment strategies.
- Coordinate collection of study specimens and processing.
- Collect and manage patient and laboratory data for clinical research projects. Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case report forms.
- Ensure compliance with research protocols and review and audit case report forms for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed.
- Assemble study kits for study visits, monitor scheduling of procedures and charges, coordinate documents, and attend monitoring meetings with sponsors, acting as primary contact.
- Monitor expenditures and adherence to study budgets and resolve billing issues in collaboration with finance and/or management staff.
- Independently performs exercise testing and outcome evaluations for patients.
- Interact with the principal investigator regularly, ensuring patient safety and adherence to proper study conduct.
- Ensure essential documentation and recording of patient and research data in appropriate files per institutional and regulatory requirements.
- Participate in monitor visits and regulatory audits.
- Other duties may also be assigned
DESIRED QUALIFICATIONS:
- Experience with database, data management, FDA regulations, IRB requirements and the Stanford clinical research environment highly desirable.
- Ability to work both independently and as part of a multidisciplinary team
- Ability to determine workload priorities in an appropriate way to accomplish tasks and goals, meet deadlines and anticipate and solve potential problems
- Experience with patients or research subjects
- Strong general computer skills and ability to quickly learn and master computer programs.
- Good oral and written communication skills to effectively work with physicians, clinical staff and other health care professionals.
- Proficiency with Microsoft Office, Word, Excel and various industry-oriented electronic data capture programs
- Excellent organizational skills and attention to detail in maintaining accurate, retrievable records
EDUCATION & EXPERIENCE (REQUIRED):
Two year college degree and two years related work experience or a Bachelor’s degree in a related field or an equivalent combination of related education and relevant experience.
KNOWLEDGE, SKILLS AND ABILITIES (REQUIRED):
- Strong interpersonal skills.
- Proficiency with Microsoft Office.
- Knowledge of medical terminology.
- Computational Skills
CERTIFICATIONS & LICENSES:
Society of Clinical Research Associates or Association of Clinical Research Professionals certification is preferred.
Physical Requirements:
- Frequently stand, walk, twist, bend, stoop, squat and use fine light/fine grasping.
- Occasionally sit, reach above shoulders, perform desk based computer tasks, use a telephone and write by hand, lift, carry, push, and pull objects that weigh up to 40 pounds.
- Rarely kneel, crawl, climb ladders, grasp forcefully, sort and file paperwork or parts, rarely lift, carry, push, and pull objects that weigh 40 pounds or more.
- Consistent with its obligations under the law, the University will provide reasonable accommodation to any employee with a disability who requires accommodation to perform the essential functions of his or her job.
WORK STANDARDS:
- Interpersonal Skills: Demonstrates the ability to work well with Stanford colleagues and clients and with external organizations.
- Promote Culture of Safety: Demonstrates commitment to personal responsibility and value for safety; communicates safety concerns; uses and promotes safe behaviors based on training and lessons learned.
- Subject to and expected to comply with all applicable University policies and procedures, including but not limited to the personnel policies and other policies found in the University's Administrative Guide, http://adminguide.stanford.edu.
The expected pay range for this position is $34.56 to $40.30 per hour.
Stanford University provides pay ranges representing its good faith estimate of the salary or hourly wage the university reasonably expects to pay for a position upon hire. The pay offered to a selected candidate will be determined based on factors such as (but not limited to) the scope and responsibilities of the position, the qualifications of the selected candidate, departmental budget availability, internal equity, geographic location, and external market pay for comparable jobs.
At Stanford University, base pay represents only one aspect of the comprehensive rewards package. The Cardinal at Work website provides detailed information on Stanford's extensive range of benefits and rewards offered to employees. Specifics about the rewards package for this position may be discussed during the hiring process.
Consistent with its obligations under the law, the University will provide reasonable accommodations to applicants and employees with disabilities. Applicants requiring a reasonable accommodation for any part of the application or hiring process should contact Stanford University Human Resources by submitting a contact form.
Stanford is an equal employment opportunity and affirmative action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by law.
The job duties listed are typical examples of work performed by positions in this job classification and are not designed to contain or be interpreted as a comprehensive inventory of all duties, tasks, and responsibilities. Specific duties and responsibilities may vary depending on department or program needs without changing the general nature and scope of the job or level of responsibility. Employees may also perform other duties as assigned.
See all 168+ Research Coordinator jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Research Coordinator roles.
Get Access To All JobsTips for Finding E-3 Visa Sponsorship as a Research Coordinator
Align your degree to the research specialty
Consular officers assess whether your Australian degree matches the specific research domain in the job offer. A public health coordinator role needs a health sciences degree, not a generic science credential. Confirm the field alignment before applying.
Target institutions with active research programs
Universities, hospital networks, and government-funded research centers file LCAs regularly for coordinator roles. Search the DOL's Foreign Labor Application Gateway to verify which employers have recent LCA certifications in your research area before reaching out.
Get your academic transcripts assessed early
Australian three-year bachelor's degrees are generally accepted for E-3 purposes, but some consular officers ask for credential evaluations. Request an official transcript with a certified English translation ready before you receive a job offer, not after.
Clarify specialty occupation status with your employer
Research Coordinator duties vary widely. Roles involving data analysis, protocol development, or regulatory submissions typically meet the specialty occupation standard. Generic administrative research roles may not. Confirm the job description specifies degree-level responsibilities before your employer files the LCA.
Use Migrate Mate's E-3 filing service for the LCA and paperwork
Once you have an offer, your employer must file a certified LCA with DOL before your visa interview. Migrate Mate's E-3 filing service manages the entire process from LCA submission through consulate appointment preparation, reducing errors that cause delays.
Book your consulate appointment before starting the role
The E-3 is consular-processed, so you attend an interview at a U.S. consulate in Australia before beginning work. Sydney, Melbourne, and Perth all process E-3 applications. Appointment availability varies by location, so schedule as soon as your LCA is certified.
Research Coordinator jobs are hiring across the US. Find yours.
Find Research Coordinator JobsResearch Coordinator E-3 Visa: Frequently Asked Questions
How do I find Research Coordinator jobs with E-3 visa sponsorship?
Migrate Mate is the most direct way to search for Research Coordinator roles where employers are open to E-3 sponsorship. Standard job boards don't filter by visa type, so you end up screening dozens of postings manually. Migrate Mate surfaces roles matched to E-3 eligibility so you can focus on applying rather than qualifying each listing.
How much does it cost to get an E-3 visa?
Migrate Mate's E-3 filing service covers the entire process for $499, including the Labor Condition Application, visa document preparation, and consulate appointment guidance. Traditional immigration lawyers charge $2,000–$5,000+ for the same work. The E-3 has less paperwork than most work visas, so paying thousands for legal help is usually unnecessary.
Does a Research Coordinator role qualify as a specialty occupation for the E-3?
It depends on the job duties. Research Coordinator positions that require designing study protocols, managing IRB submissions, analyzing data, or overseeing regulatory compliance typically satisfy the specialty occupation standard because they require at minimum a bachelor's degree in a specific field. Roles limited to scheduling, data entry, or general administration are less likely to qualify. The job description needs to reflect degree-level responsibilities explicitly.
How does the E-3 compare to the H-1B for Research Coordinator roles?
The E-3 is available only to Australian citizens, but it has a significant practical advantage: there is no lottery. H-1B selection is capped at 85,000 registrations per year and is subject to a random draw, meaning qualified candidates are frequently not selected. The E-3 cap of 10,500 has never been reached, so a qualified Australian applicant with a job offer and certified LCA can proceed to interview without waiting for a lottery result.
Can I change employers while on an E-3 as a Research Coordinator?
Yes, but you need to restart the process with your new employer. The E-3 is employer-specific, meaning your current visa stamp is tied to the sponsoring institution. Your new employer must file a fresh LCA with DOL, and in most cases you'll need to attend a new consulate interview in Australia to obtain an updated E-3 visa stamp before beginning the new role.
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