E-3 Visa Clinical Research Coordinator Jobs
Clinical Research Coordinator roles qualify for E-3 visa sponsorship when tied to a bachelor's degree in life sciences, public health, or a related field. Australian professionals bring GCP training and trial management experience that U.S. sponsors value, and the E-3's unlimited two-year renewals make long-term placements practical for both sides.
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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 149+ Clinical Research Coordinator jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Research Coordinator roles.
Get Access To All JobsTips for Finding E-3 Visa Sponsorship as a Clinical Research Coordinator
Translate your Australian credentials for U.S. employers
Your three-year Australian bachelor's degree is generally accepted as equivalent to a U.S. four-year degree for E-3 purposes. Pair it with a certified transcript and, if your degree is in a loosely related field, a credential evaluation letter that maps your coursework to clinical research.
Target sponsors with active IND or NDA trial portfolios
Pharmaceutical companies running active Investigational New Drug or New Drug Application trials file LCAs regularly and have established HR processes for international hires. Academic medical centers affiliated with teaching hospitals are another consistent source of E-3-eligible CRC roles.
Clarify specialty occupation status before applying
Not every CRC posting qualifies as a specialty occupation. Job ads requiring only an associate degree or listing the degree as preferred rather than required can create problems at the consulate. Confirm the posting states a bachelor's degree in a specific field as a minimum requirement before investing time in an application.
Understand how the LCA filing affects your start date
Your employer must obtain a certified LCA from the DOL before your consulate appointment. DOL targets seven business days for LCA certification, but incomplete wage documentation can extend that window. Build at least three weeks into your timeline between offer acceptance and your intended start date.
Use Migrate Mate's E-3 filing service to coordinate LCA and consulate prep
CRC sponsorship requires the employer to certify prevailing wage compliance and you to prepare a matching DS-160 and supporting documents. Migrate Mate's E-3 filing service manages the entire process from offer to consulate appointment, reducing the back-and-forth between you and your HR team.
Negotiate a conditional start date tied to visa approval
E-3 consulate appointments at Sydney, Melbourne, or Perth can book out several weeks. Ask your employer to structure your offer letter with a start date contingent on visa approval rather than a fixed calendar date, so a brief scheduling delay doesn't put your offer at risk.
Clinical Research Coordinator jobs are hiring across the US. Find yours.
Find Clinical Research Coordinator JobsClinical Research Coordinator E-3 Visa: Frequently Asked Questions
How do I find Clinical Research Coordinator jobs with E-3 visa sponsorship?
Migrate Mate lets you search CRC openings filtered specifically by E-3 visa sponsorship, so you're not sifting through roles that won't support your status. Because the E-3 requires employer action before your consulate appointment, targeting companies already familiar with the LCA process saves significant time and reduces the risk of a withdrawn offer.
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 Clinical Research Coordinator role qualify as a specialty occupation for the E-3?
Yes, provided the position requires a bachelor's degree in a specific field such as life sciences, public health, nursing, or a closely related discipline. Roles requiring only general education, or where the degree is listed as preferred rather than required, may not meet the specialty occupation standard at the consulate. Always confirm the job description explicitly states a field-specific degree as the minimum.
How does the E-3 visa compare to the H-1B for Clinical Research Coordinators?
The E-3 is available only to Australian citizens, but it has no annual lottery and no cap that realistically fills. H-1B selection runs around 25% for most registrants, meaning most applicants don't get a slot in a given year. For Australian CRCs, the E-3 is a direct path: your employer files an LCA, you attend a consulate appointment, and you can start working. There's no lottery delay and no waiting until October 1.
Can I switch CRC employers while on an E-3 visa?
Yes, but you need a new LCA and a new E-3 visa stamp issued by a U.S. consulate before starting with the new employer. Unlike H-1B portability, the E-3 doesn't allow you to begin work for a new employer while the petition is pending. Plan for two to four weeks of lead time between accepting a new offer and your available start date.
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