Clinical Trial Associate Jobs at University of Miami with Visa Sponsorship
Clinical Trial Associate roles at University of Miami sit within a research-intensive academic medical environment, supporting federally regulated clinical studies across its health system. The university has an established process for sponsoring international researchers and clinical professionals, making it a realistic target for candidates who need work authorization.
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CORE JOB SUMMARY
The Senior Research Associate 2, GAB ensures that the operations of the assigned laboratory are efficient and in compliance with applicable guidelines and regulations. Moreover, this employee engages in complex and specialized research activities in furtherance of the University’s research goals and objectives.
The Senior Research Associate II supports ECHO biospecimen processing and performs laboratory experiments across multiple research projects within the lab. This role requires demonstrated technical proficiency in molecular and cellular laboratory techniques, the ability to execute experimental protocols independently, and the capacity to maintain sample integrity across both standardized and research-driven workflows.
CORE JOB FUNCTIONS
-
Contributes to basic and applied research activities by collecting and analyzing data and maintaining databases.
-
Understands and interprets research protocols and procedures.
-
Participates in the publication of significant results.
-
Advances expertise through continued education, training, and research.
-
Maintains an overview of relevant research findings.
-
Ensures all research is undertaken according to good research practice.
-
Stays abreast of developments in the field which may impact department functions.
-
Provides guidance, mentorship, and oversight to junior research staff and students.
-
Adheres to University and unit-level policies and procedures and safeguards University assets.
Core Responsibilities
-
Perform all ECHO biospecimen processing activities, including aliquoting, labeling, storage, and shipment preparation.
-
Maintain sample integrity, chain of custody, and accurate tracking for all specimens.
-
Conduct laboratory experiments across multiple research projects using established protocols.
-
Perform sample preparation and processing for downstream molecular and biochemical assays.
-
Execute and document experimental procedures with accuracy and consistency.
-
Operate, maintain, and troubleshoot laboratory equipment used in experimental workflows.
-
Maintain compliance with laboratory safety, regulatory, and quality standards.
-
Support inventory management across both ECHO and non-ECHO lab activities.
This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.
CORE QUALIFICATIONS
Education:
Master's degree in relevant field required.
Experience:
Minimum 1 year of relevant experience required.
Certification and Licensing:
Refer to department description for applicable certification requirements.
Required Technical Competencies
Candidates must demonstrate hands-on experience with multiple of the following:
- Tissue culture and basic cell culture techniques
- Microscopy (e.g., fluorescence, brightfield imaging)
- ELISA and plate-based assays
- RT-qPCR and nucleic acid quantification
- DNA and RNA isolation and purification
- Protein-based assays (e.g., Western blotting)
- Multiplex assay platforms
- Sample preparation for mass spectrometry (MS/MS)
- General molecular biology and biochemical laboratory techniques
Scope of Role
- Supports both standardized ECHO workflows and complex experimental lab work
- Requires independent execution of laboratory techniques and protocols
- Functions across multiple research efforts, requiring adaptability and technical breadth
- Involves higher responsibility for data quality and experimental integrity
Minimum Qualifications
- Bachelor’s degree in biology, Molecular Biology, Biochemistry, or related field strongly preferred
- Minimum 3 years of hands-on laboratory experience in a research setting
- Demonstrated experience performing molecular and/or cellular laboratory techniques
- Ability to work independently and manage multiple technical workflows
- Familiarity with regulatory compliance processes, including IRB submissions and HIPAA guidelines
- Phlebotomy certified and trained, or willingness to obtain phlebotomy certification and training
Key Responsibilities:
- Research Coordination, Implementation, and Leadership
- Serves as lead coordinator for community-based and clinic-based studies focused on cancer.
- Monitors data integrity and ensures that all project activities adhere to protocol and regulatory requirements.
- Works closely with Principal Investigators and managers to develop and refine study protocols, data collection instruments, recruitment plans, and timelines.
- Acts as the primary point of contact for internal and external stakeholders, including collaborators, principal investigators, and regulatory staff.
- Oversees study implementation across multiple community and clinical sites.
- Coordinates project timelines, staffing plans, and site logistics.
- Collaborates with investigators on protocol adaptations and operational planning.
Participant and Community Engagement:
- Conducts periodic performance assessments and supports the professional development of team members.
- Assists managers with study launch, monitors milestones, and ensures seamless communication between internal teams and external partners.
Data Collection Documentation and Quality Assurance:
- Leads data management efforts, including database design, quality control, integrity monitoring, and qualitative analysis.
- Coordinates the work of entry-level research associates to ensure data is being collected effectively for assigned research studies.
- Prepares enrollment summaries, interim reports, and final project deliverables for internal use and reporting to SCCC managers.
- If certified/trained in phlebotomy, performs venipuncture and collects laboratory samples in accordance with study protocols.
- Prepares documentation for sponsor audits and monitoring visits.
- Conducts and oversees interviews and focus groups.
Administrative & Operational Duties:
- Monitors study supply inventory and assists Senior Research Associates with ordering study-related supplies.
- If certified/trained in phlebotomy, performs venipuncture blood collections and collects laboratory samples in accordance with study protocols.
- Collects, processes, packs, and ships specimens (blood, saliva, urine, fecal, etc.) according to protocol, applicable standards and regulations, and coordinates with appropriate laboratories for drop off and storage.
- Supports manuscript preparations, abstract submissions, and conference logistics.
Training and Team Integration:
- Engage in professional development and learning activities to enhance research capabilities.
- Collaborates with multidisciplinary team members to ensure timely and high-quality execution of research activities.
- Training and supervision of lower-level research associates and research trainees.
- Supports managers with team onboarding and continuing education activities.
- Provide project-specific guidance and oversee quality control for field and office activities.
- Ensures consistency and standardization of study implementation across the team.
Supervision and Mentorship:
- Provides direct supervision, guidance, and mentorship to junior research staff, including Research Associate 1 and 2 and Research Support Specialist team members.
- Provide training on research methods, data collection tools, community engagement best practices, and regulatory compliance.
- Serves as study lead on multiple research projects, coordinating all aspects of protocol implementation.
- Acts as the primary point of contact for internal and external stakeholders, including collaborators, sponsors, and regulatory offices.
The University of Miami is recognized as one of the nation’s premier research institutions and academic health systems and is among the largest employers in South Florida.
With more than 20,000 faculty and staff, the University is committed to excellence and guided by a mission to positively impact the lives of students, patients, and communities locally and globally.
We are dedicated to fostering a culture where every individual feels valued and empowered to contribute meaningfully. United by shared values, the University community works together to build an environment defined by purpose, collaboration, and service.
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information.
Job Status:
Full time
Employee Type:
Staff

CORE JOB SUMMARY
The Senior Research Associate 2, GAB ensures that the operations of the assigned laboratory are efficient and in compliance with applicable guidelines and regulations. Moreover, this employee engages in complex and specialized research activities in furtherance of the University’s research goals and objectives.
The Senior Research Associate II supports ECHO biospecimen processing and performs laboratory experiments across multiple research projects within the lab. This role requires demonstrated technical proficiency in molecular and cellular laboratory techniques, the ability to execute experimental protocols independently, and the capacity to maintain sample integrity across both standardized and research-driven workflows.
CORE JOB FUNCTIONS
-
Contributes to basic and applied research activities by collecting and analyzing data and maintaining databases.
-
Understands and interprets research protocols and procedures.
-
Participates in the publication of significant results.
-
Advances expertise through continued education, training, and research.
-
Maintains an overview of relevant research findings.
-
Ensures all research is undertaken according to good research practice.
-
Stays abreast of developments in the field which may impact department functions.
-
Provides guidance, mentorship, and oversight to junior research staff and students.
-
Adheres to University and unit-level policies and procedures and safeguards University assets.
Core Responsibilities
-
Perform all ECHO biospecimen processing activities, including aliquoting, labeling, storage, and shipment preparation.
-
Maintain sample integrity, chain of custody, and accurate tracking for all specimens.
-
Conduct laboratory experiments across multiple research projects using established protocols.
-
Perform sample preparation and processing for downstream molecular and biochemical assays.
-
Execute and document experimental procedures with accuracy and consistency.
-
Operate, maintain, and troubleshoot laboratory equipment used in experimental workflows.
-
Maintain compliance with laboratory safety, regulatory, and quality standards.
-
Support inventory management across both ECHO and non-ECHO lab activities.
This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.
CORE QUALIFICATIONS
Education:
Master's degree in relevant field required.
Experience:
Minimum 1 year of relevant experience required.
Certification and Licensing:
Refer to department description for applicable certification requirements.
Required Technical Competencies
Candidates must demonstrate hands-on experience with multiple of the following:
- Tissue culture and basic cell culture techniques
- Microscopy (e.g., fluorescence, brightfield imaging)
- ELISA and plate-based assays
- RT-qPCR and nucleic acid quantification
- DNA and RNA isolation and purification
- Protein-based assays (e.g., Western blotting)
- Multiplex assay platforms
- Sample preparation for mass spectrometry (MS/MS)
- General molecular biology and biochemical laboratory techniques
Scope of Role
- Supports both standardized ECHO workflows and complex experimental lab work
- Requires independent execution of laboratory techniques and protocols
- Functions across multiple research efforts, requiring adaptability and technical breadth
- Involves higher responsibility for data quality and experimental integrity
Minimum Qualifications
- Bachelor’s degree in biology, Molecular Biology, Biochemistry, or related field strongly preferred
- Minimum 3 years of hands-on laboratory experience in a research setting
- Demonstrated experience performing molecular and/or cellular laboratory techniques
- Ability to work independently and manage multiple technical workflows
- Familiarity with regulatory compliance processes, including IRB submissions and HIPAA guidelines
- Phlebotomy certified and trained, or willingness to obtain phlebotomy certification and training
Key Responsibilities:
- Research Coordination, Implementation, and Leadership
- Serves as lead coordinator for community-based and clinic-based studies focused on cancer.
- Monitors data integrity and ensures that all project activities adhere to protocol and regulatory requirements.
- Works closely with Principal Investigators and managers to develop and refine study protocols, data collection instruments, recruitment plans, and timelines.
- Acts as the primary point of contact for internal and external stakeholders, including collaborators, principal investigators, and regulatory staff.
- Oversees study implementation across multiple community and clinical sites.
- Coordinates project timelines, staffing plans, and site logistics.
- Collaborates with investigators on protocol adaptations and operational planning.
Participant and Community Engagement:
- Conducts periodic performance assessments and supports the professional development of team members.
- Assists managers with study launch, monitors milestones, and ensures seamless communication between internal teams and external partners.
Data Collection Documentation and Quality Assurance:
- Leads data management efforts, including database design, quality control, integrity monitoring, and qualitative analysis.
- Coordinates the work of entry-level research associates to ensure data is being collected effectively for assigned research studies.
- Prepares enrollment summaries, interim reports, and final project deliverables for internal use and reporting to SCCC managers.
- If certified/trained in phlebotomy, performs venipuncture and collects laboratory samples in accordance with study protocols.
- Prepares documentation for sponsor audits and monitoring visits.
- Conducts and oversees interviews and focus groups.
Administrative & Operational Duties:
- Monitors study supply inventory and assists Senior Research Associates with ordering study-related supplies.
- If certified/trained in phlebotomy, performs venipuncture blood collections and collects laboratory samples in accordance with study protocols.
- Collects, processes, packs, and ships specimens (blood, saliva, urine, fecal, etc.) according to protocol, applicable standards and regulations, and coordinates with appropriate laboratories for drop off and storage.
- Supports manuscript preparations, abstract submissions, and conference logistics.
Training and Team Integration:
- Engage in professional development and learning activities to enhance research capabilities.
- Collaborates with multidisciplinary team members to ensure timely and high-quality execution of research activities.
- Training and supervision of lower-level research associates and research trainees.
- Supports managers with team onboarding and continuing education activities.
- Provide project-specific guidance and oversee quality control for field and office activities.
- Ensures consistency and standardization of study implementation across the team.
Supervision and Mentorship:
- Provides direct supervision, guidance, and mentorship to junior research staff, including Research Associate 1 and 2 and Research Support Specialist team members.
- Provide training on research methods, data collection tools, community engagement best practices, and regulatory compliance.
- Serves as study lead on multiple research projects, coordinating all aspects of protocol implementation.
- Acts as the primary point of contact for internal and external stakeholders, including collaborators, sponsors, and regulatory offices.
The University of Miami is recognized as one of the nation’s premier research institutions and academic health systems and is among the largest employers in South Florida.
With more than 20,000 faculty and staff, the University is committed to excellence and guided by a mission to positively impact the lives of students, patients, and communities locally and globally.
We are dedicated to fostering a culture where every individual feels valued and empowered to contribute meaningfully. United by shared values, the University community works together to build an environment defined by purpose, collaboration, and service.
The University of Miami is an Equal Opportunity Employer. Applicants and employees are protected from discrimination based on certain categories protected by Federal law. Click here for additional information.
Job Status:
Full time
Employee Type:
Staff
See all 36+ Clinical Trial Associate at University of Miami jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Trial Associate at University of Miami roles.
Get Access To All JobsTips for Finding Clinical Trial Associate Jobs at University of Miami Jobs
Align your credentials with GCP requirements
University of Miami's clinical trials operation runs under strict FDA and ICH Good Clinical Practice standards. Before applying, document any GCP certification, IRB experience, or protocol deviation training on your resume. Academic medical centers scrutinize regulatory competency early in screening.
Target postings through UM's research departments
Clinical Trial Associate openings at University of Miami often originate from specific research units like the Sylvester Comprehensive Cancer Center or the Miller School of Medicine. Searching by department rather than job title alone surfaces roles before they're widely circulated.
Clarify your OPT or CPT timeline during outreach
If you're on F-1 status, University of Miami's HR team will want to know your OPT expiration date upfront. A 24-month STEM extension is possible if your degree qualifies, giving the university enough runway to file an H-1B petition before your authorization lapses.
Understand how H-1B cap timing affects your start date
H-1B petitions for university research roles are often cap-exempt under USCIS rules for higher education institutions, meaning University of Miami can file year-round rather than waiting for the April lottery. Confirm this status with the employer during the offer stage so your start date isn't delayed unnecessarily.
Request the LCA before signing your offer letter
Your employer files the Labor Condition Application with DOL before USCIS receives your H-1B petition. Asking for the LCA posting notice timeline signals you understand the process and helps you anticipate when you can realistically begin work in a formal capacity.
Browse Clinical Trial Associate openings on Migrate Mate
Filtering by visa sponsorship type saves time when you're targeting roles that match your authorization. Use Migrate Mate to identify University of Miami's active Clinical Trial Associate postings and cross-reference which positions explicitly support the visa category you need.
Clinical Trial Associate at University of Miami jobs are hiring across the US. Find yours.
Find Clinical Trial Associate at University of Miami JobsFrequently Asked Questions
Does University of Miami sponsor H-1B visas for Clinical Trial Associates?
Yes. University of Miami qualifies as a higher education institution under USCIS guidelines, which means it can file H-1B petitions as a cap-exempt employer year-round. For Clinical Trial Associates, this is significant because it removes the April lottery constraint that affects most private-sector employers. You can start the petition process as soon as you have a signed offer, rather than waiting for a specific registration window.
How do I apply for Clinical Trial Associate jobs at University of Miami?
Applications go through University of Miami's Careers portal at careers.miami.edu. Search for Clinical Trial Associate or CRA roles and filter by the research unit you want to target, such as the Sylvester Comprehensive Cancer Center or Miller School of Medicine. Tailor your application to highlight GCP certification, protocol management experience, and any familiarity with IRB submissions. Migrate Mate also lists University of Miami's sponsored openings, filtered by visa type, so you can confirm sponsorship eligibility before applying.
Which visa types does University of Miami commonly use for Clinical Trial Associate roles?
The H-1B is the most common long-term work visa for Clinical Trial Associates at University of Miami, given that Clinical Research is generally recognized as a specialty occupation requiring at least a bachelor's degree in a relevant field. The university also supports F-1 OPT and CPT for recent graduates, J-1 for exchange visitors in qualifying research programs, and TN visas for Canadian and Mexican nationals in eligible occupational categories. EB-2 and EB-3 immigrant visa pathways are available for candidates pursuing permanent residence.
What qualifications does University of Miami expect for Clinical Trial Associate roles?
Most postings require a bachelor's degree in a life sciences field such as biology, nursing, public health, or a related discipline. GCP certification and direct experience with clinical trial documentation, including source data verification, case report forms, and protocol deviation reporting, are consistently listed as requirements. Familiarity with FDA regulations and electronic data capture systems like REDCap or Medidata Rave strengthens your application considerably. Academic medical center experience is a differentiator for higher-level CTA roles.
How long does the visa sponsorship process take for a Clinical Trial Associate position at University of Miami?
If you're on F-1 OPT, the university can file an H-1B petition as a cap-exempt institution at any point during the year, with standard USCIS processing taking roughly three to six months. Premium processing, which expedites adjudication to 15 business days, is available for an additional fee and is worth discussing with the HR or immigration team during the offer stage. The Labor Condition Application with DOL typically takes seven to ten business days to certify and must be completed before USCIS receives the H-1B petition.
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