E-3 Visa Clinical Support Associate Jobs
Clinical Support Associate roles in the U.S. qualify for E-3 visa sponsorship when tied to a bachelor's degree in a health sciences, biomedical, or clinical field. The E-3 has no lottery and renews indefinitely in two-year increments, making it a stable path for Australian professionals entering U.S. clinical environments.
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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 346+ Clinical Support Associate jobs
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Get Access To All JobsTips for Finding E-3 Visa Sponsorship as a Clinical Support Associate
Align your Australian credentials to U.S. standards
A three-year Australian bachelor's in health sciences, biomedical science, or a related clinical field is generally accepted as equivalent to a U.S. four-year degree. Confirm this equivalency in writing before your employer begins the LCA filing.
Target healthcare systems with active LCA histories
Focus your search on hospital networks, academic medical centers, and clinical research organizations that have previously filed Labor Condition Applications for clinical roles. DOL's public LCA disclosure data lets you verify which employers have done this before.
Clarify the specialty occupation question early
Some Clinical Support Associate postings list a degree as preferred rather than required. A job description that doesn't mandate a specific degree can complicate E-3 approval. Ask the hiring manager to confirm the role requires a bachelor's in a relevant field before you advance.
Use Migrate Mate's E-3 filing service for the full process
Once you have an offer, use Migrate Mate's E-3 filing service to handle your LCA and visa paperwork end-to-end. This covers DOL certification, consulate preparation, and document review so your employer isn't navigating the process alone for the first time.
Prepare your clinical documentation before the offer stage
Gather your degree transcripts, any clinical certifications, and a letter confirming your job duties before interviews progress to the offer stage. Consulates in Sydney, Melbourne, and Perth can ask for supporting documentation that connects your qualifications directly to the role.
Address E-3 eligibility directly during offer negotiation
Many U.S. healthcare employers are unfamiliar with the E-3 specifically. When the offer conversation begins, explain that the E-3 requires no lottery, has a fast DOL certification timeline, and places minimal filing burden on them compared to an H-1B petition.
Clinical Support Associate jobs are hiring across the US. Find yours.
Find Clinical Support Associate JobsClinical Support Associate E-3 Visa: Frequently Asked Questions
How do I find Clinical Support Associate jobs with E-3 visa sponsorship?
Migrate Mate is built specifically for Australian professionals searching for U.S. roles with E-3 sponsorship. Rather than filtering through general job boards, Migrate Mate surfaces Clinical Support Associate positions at employers already familiar with or open to the E-3 process, saving you the work of screening employers who can't or won't sponsor.
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 Support Associate role qualify as a specialty occupation for the E-3?
It can, but the job description matters. The role must require at least a bachelor's degree in a specific field such as health sciences, biomedical science, or clinical research to meet the E-3 specialty occupation standard. If the posting describes the degree as preferred or substitutable with experience, your employer may need to revise the job description before the LCA is filed with DOL.
How does the E-3 compare to the H-1B for a Clinical Support Associate?
The E-3 has no annual cap and no lottery, so you can apply at any time of year and expect a decision based on your qualifications rather than a random draw. The H-1B is subject to an 85,000-slot annual cap with a lottery selection rate well below 50% for most registrants. For a Clinical Support Associate with an Australian passport, the E-3 is a significantly more predictable path.
Can I transfer my E-3 to a new Clinical Support Associate employer if I change roles?
Yes, but you'll need to start the process over with the new employer. The E-3 is employer-specific, so your new employer must file a fresh LCA with DOL and you'll need to attend a new consular interview in Australia to get an updated visa stamp. There's no portability provision equivalent to what H-1B holders have under AC21.
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