E-3 Visa Clinical Data Analyst Jobs
Clinical Data Analyst roles qualify for E-3 visa sponsorship as specialty occupations requiring a bachelor's degree in a quantitative or health sciences field. Australian nationals can secure two-year renewals indefinitely, with no lottery and no annual cap limiting your options the way H-1B does.
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Associate Director, Clinical Database Applications and Reporting
Job Requisition ID:
1408
Posting Start Date:
4/27/26
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
Job Summary
The Associate Director, Clinical Database Applications and Reporting is a member of the Biostatistics and Data Management team and serves as a subject matter expert responsible for setting the overall programming strategy including the oversight, guidance, implementation, and management of clinical database applications and reporting.
The responsibilities include advancing operational excellence by standardizing reporting, scaling programming strategies, automating workflows, and delivering high-quality outputs that meet user requirements by collaborating with a variety of internal and external stakeholders including leading all aspects of end-to-end programming efforts.
In addition managing quality of data validation programming deliverables; maintaining compliance and inspection readiness of clinical applications, reports, and supporting process documentation; and reporting process are some of the key requirements of the role.
This position provides expertise within Data Management by partnering with internal and external stakeholders (e.g. DM Portfolio Delivery, Data Acquisition & Processing, Precision Medicine, CROs, External Vendors, etc.) to optimize data programming services on behalf of Daiichi Sankyo.
In addition, excellent verbal/written skills, analytical, organizational, and interpersonal skills for working effectively with people at different levels are some of the requirements of this role. This position requires skills in working in a fast-paced environment, continuous improvement, project management, change and risk management.
Responsibilities
Leadership, Direction, and Strategy:
- Establish programming strategy in designing, developing, and maintaining reporting business needs, including programming capabilities assessment, technology and infrastructure requirements of new and/or existing clinical database applications and reporting solutions.
- Act as a subject matter expert in advanced clinical data programming, data transformation, visualization, and emerging technologies to elevate and modernize internal reporting capabilities.
- Provide operational leadership and management of clinical database applications and reporting solutions to address business needs consistent with regulatory requirements including GxP, 21 CFR Part-11, data protection and privacy requirements.
- Ensure programming related technical and end user support to other areas of Data Acquisition & Processing, for the development of reports, data listings, and data visualizations consistent with study requirements and integrated data review plans.
- Manage direct reports including the development, coaching, and mentoring of team members.
Project Management:
- Drive successful delivery of clinical data management programming objectives by aligning priorities, streamlining workflows, and optimizing resources in collaboration with cross-functional stakeholders.
- Ensure effective quality oversight of the core clinical database applications and reporting, supporting processes, technology, and infrastructure improvements; maintain audit and inspection readiness of all the deliverables.
- Oversee the quality of data listings, reports, patient profiles, and metrics, ensuring high-quality, timely outputs that support operational insights in line with integrated data review plans.
- Manage and maintain standard library of data listings and reporting objects to maximize reuse, efficiency, productivity, and standardization.
- Manage data exchange agreements and deliver quality data extracts for internal and external stakeholder consumption compliant with regulatory, data protection, and data privacy requirements.
Functional Expertise:
- Serve as a subject matter expert for the oversight, guidance, implementation, and management of clinical applications and reporting solutions with expertise in Data Management Systems.
- Support the integration of clinical data from CRF and non-CRF data sources to streamline workflow, improve efficiencies, and quality of data management processes and deliverables.
- Serve as a trusted SME in clinical data management programming and reporting, leading resolution of complex issues and guiding internal teams and external partners to achieve successful outcomes.
- Partner with clinical database programming, external data acquisition & management, study data managers, and external vendors to perform quality checks for the reconciliation of external data with EDC.
- Contribute to the development of standard and custom reports and data listings specifications; develop and evaluate complex listings and reports including patient profiles, dose modification listings, exception listings, medical coding, among others to support critical and time-sensitive study milestones.
- Collaborate with the clinical database programming group to create, manage, and maintain validated toolsets, macros, and automated scripts for code optimization and standardization to maximize efficiencies, consistency, and quality of the outputs.
- Explore novel and automated approaches to data extractions, data wrangling, and contextualizing data assets to develop innovative solutions compliant to regulatory, data protection and privacy requirements.
- Establish appropriate SOP/SOIs, work procedures/guidance, job aids, and trackers to guide the operational use of custom reports, data listings, and data visualizations for study needs.
Operational Efficiency / Continuous Improvement:
- Identify and address areas of gaps, and opportunities to enhance and improve operational efficiencies and productivity through automation, code optimization and standardization, process improvements, and improving the quality of actionable insights.
- Proactively identify risks and mitigation approaches to overcome impediments and improve operational efficiencies.
Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Education
Bachelor's Degree or higher in life sciences or related field required
Master's Degree in life sciences or related field preferred
Work Experience
- Minimum of 7 years of Global Clinical Trial experience in the device/pharmaceutical/CRO industry with expertise in clinical database programming, methods, and techniques supporting Clinical Data Management systems and services required.
- Skilled in areas of data validation programming, creating complex data listings, reports, and data visualizations; reconciliation of external data; expertise in industry standard reporting required.
- Experience with data visualization tools such as Qlik, Spotfire, Tableau, Power BI, JReview, SAS, Domo, among others required.
- Knowledge of CDASH and CDISC data standards; knowledge of data acquisition, aggregation, contextualization, integration tools, and technologies required.
Competencies
- Strong knowledge and techniques of data extraction, data wrangling, exploration, and contextualization of data assets in clinical domain.
- Expertise in data validation programming and analysis proficiency with SAS tools, SQL, and Python/R.
- Deep experience working with a variety of industry standard reporting and data visualization tools for data insights, data listings, and custom reports.
- Proficient in industry standards, medical terminology, and clinical trial methodologies.
- Knowledge and awareness of industry trends, best practices, and emerging technologies for data collection, management, reporting and analytics.
- Knowledge of industry standard commercial clinical systems such as EDC, CTMS, IRT, CDR, and eTMF.
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range:
USD$153,600.00 - USD$230,400.00
Job Title:
Associate Director, Clinical Database Applications and Reporting
Job Requisition ID:
1408
Posting Start Date:
4/27/26
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
Job Summary
The Associate Director, Clinical Database Applications and Reporting is a member of the Biostatistics and Data Management team and serves as a subject matter expert responsible for setting the overall programming strategy including the oversight, guidance, implementation, and management of clinical database applications and reporting.
The responsibilities include advancing operational excellence by standardizing reporting, scaling programming strategies, automating workflows, and delivering high-quality outputs that meet user requirements by collaborating with a variety of internal and external stakeholders including leading all aspects of end-to-end programming efforts.
In addition managing quality of data validation programming deliverables; maintaining compliance and inspection readiness of clinical applications, reports, and supporting process documentation; and reporting process are some of the key requirements of the role.
This position provides expertise within Data Management by partnering with internal and external stakeholders (e.g. DM Portfolio Delivery, Data Acquisition & Processing, Precision Medicine, CROs, External Vendors, etc.) to optimize data programming services on behalf of Daiichi Sankyo.
In addition, excellent verbal/written skills, analytical, organizational, and interpersonal skills for working effectively with people at different levels are some of the requirements of this role. This position requires skills in working in a fast-paced environment, continuous improvement, project management, change and risk management.
Responsibilities
Leadership, Direction, and Strategy:
- Establish programming strategy in designing, developing, and maintaining reporting business needs, including programming capabilities assessment, technology and infrastructure requirements of new and/or existing clinical database applications and reporting solutions.
- Act as a subject matter expert in advanced clinical data programming, data transformation, visualization, and emerging technologies to elevate and modernize internal reporting capabilities.
- Provide operational leadership and management of clinical database applications and reporting solutions to address business needs consistent with regulatory requirements including GxP, 21 CFR Part-11, data protection and privacy requirements.
- Ensure programming related technical and end user support to other areas of Data Acquisition & Processing, for the development of reports, data listings, and data visualizations consistent with study requirements and integrated data review plans.
- Manage direct reports including the development, coaching, and mentoring of team members.
Project Management:
- Drive successful delivery of clinical data management programming objectives by aligning priorities, streamlining workflows, and optimizing resources in collaboration with cross-functional stakeholders.
- Ensure effective quality oversight of the core clinical database applications and reporting, supporting processes, technology, and infrastructure improvements; maintain audit and inspection readiness of all the deliverables.
- Oversee the quality of data listings, reports, patient profiles, and metrics, ensuring high-quality, timely outputs that support operational insights in line with integrated data review plans.
- Manage and maintain standard library of data listings and reporting objects to maximize reuse, efficiency, productivity, and standardization.
- Manage data exchange agreements and deliver quality data extracts for internal and external stakeholder consumption compliant with regulatory, data protection, and data privacy requirements.
Functional Expertise:
- Serve as a subject matter expert for the oversight, guidance, implementation, and management of clinical applications and reporting solutions with expertise in Data Management Systems.
- Support the integration of clinical data from CRF and non-CRF data sources to streamline workflow, improve efficiencies, and quality of data management processes and deliverables.
- Serve as a trusted SME in clinical data management programming and reporting, leading resolution of complex issues and guiding internal teams and external partners to achieve successful outcomes.
- Partner with clinical database programming, external data acquisition & management, study data managers, and external vendors to perform quality checks for the reconciliation of external data with EDC.
- Contribute to the development of standard and custom reports and data listings specifications; develop and evaluate complex listings and reports including patient profiles, dose modification listings, exception listings, medical coding, among others to support critical and time-sensitive study milestones.
- Collaborate with the clinical database programming group to create, manage, and maintain validated toolsets, macros, and automated scripts for code optimization and standardization to maximize efficiencies, consistency, and quality of the outputs.
- Explore novel and automated approaches to data extractions, data wrangling, and contextualizing data assets to develop innovative solutions compliant to regulatory, data protection and privacy requirements.
- Establish appropriate SOP/SOIs, work procedures/guidance, job aids, and trackers to guide the operational use of custom reports, data listings, and data visualizations for study needs.
Operational Efficiency / Continuous Improvement:
- Identify and address areas of gaps, and opportunities to enhance and improve operational efficiencies and productivity through automation, code optimization and standardization, process improvements, and improving the quality of actionable insights.
- Proactively identify risks and mitigation approaches to overcome impediments and improve operational efficiencies.
Qualifications
To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
Education
Bachelor's Degree or higher in life sciences or related field required
Master's Degree in life sciences or related field preferred
Work Experience
- Minimum of 7 years of Global Clinical Trial experience in the device/pharmaceutical/CRO industry with expertise in clinical database programming, methods, and techniques supporting Clinical Data Management systems and services required.
- Skilled in areas of data validation programming, creating complex data listings, reports, and data visualizations; reconciliation of external data; expertise in industry standard reporting required.
- Experience with data visualization tools such as Qlik, Spotfire, Tableau, Power BI, JReview, SAS, Domo, among others required.
- Knowledge of CDASH and CDISC data standards; knowledge of data acquisition, aggregation, contextualization, integration tools, and technologies required.
Competencies
- Strong knowledge and techniques of data extraction, data wrangling, exploration, and contextualization of data assets in clinical domain.
- Expertise in data validation programming and analysis proficiency with SAS tools, SQL, and Python/R.
- Deep experience working with a variety of industry standard reporting and data visualization tools for data insights, data listings, and custom reports.
- Proficient in industry standards, medical terminology, and clinical trial methodologies.
- Knowledge and awareness of industry trends, best practices, and emerging technologies for data collection, management, reporting and analytics.
- Knowledge of industry standard commercial clinical systems such as EDC, CTMS, IRT, CDR, and eTMF.
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range:
USD$153,600.00 - USD$230,400.00
See all 52+ Clinical Data Analyst jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Data Analyst roles.
Get Access To All JobsTips for Finding E-3 Visa Sponsorship as a Clinical Data Analyst
Translate your Australian credentials early
U.S. employers evaluate degrees against their own four-year standard. A three-year Australian bachelor's in biostatistics, epidemiology, or health informatics is generally accepted, but have a credential evaluation letter ready before your first technical interview.
Target companies with active LCA filings
Search the DOL's Office of Foreign Labor Certification disclosure data for Clinical Data Analyst LCA filings. Employers who have certified LCAs recently already understand the E-3 process and won't need educating during your offer negotiation.
Clarify specialty occupation fit in your application
Not every analyst role qualifies as a specialty occupation. Roles requiring statistical programming in SAS or R, clinical trial data management, or regulatory submission support are stronger E-3 candidates than general reporting positions. Tailor your resume to highlight those specifics.
Get your LCA filed before booking your consulate appointment
The LCA must be certified by the DOL before you can attend your visa interview. Use Migrate Mate's E-3 filing service to handle your LCA and visa paperwork so the sequence is correct and your consulate appointment isn't wasted.
Address employer reluctance with E-3 process facts
Many U.S. hiring managers conflate E-3 with H-1B and assume a lottery is involved. Explaining that the E-3 has no cap, no lottery, and that employer-side steps are limited to LCA certification often removes the hesitation before it becomes a hard no.
Confirm your job offer letter specifies degree requirements
Your offer letter must state that the role requires a relevant bachelor's degree or equivalent. Consular officers scrutinize this for specialty occupation eligibility. A vague offer letter that omits degree requirements can trigger additional questioning at your interview.
Clinical Data Analyst jobs are hiring across the US. Find yours.
Find Clinical Data Analyst JobsClinical Data Analyst E-3 Visa: Frequently Asked Questions
How do I find Clinical Data Analyst jobs with E-3 visa sponsorship?
Migrate Mate is built specifically for this search. It surfaces Clinical Data Analyst roles where employers have demonstrated willingness to sponsor E-3 visas, so you're not filtering through listings that will never result in sponsorship. Standard job boards don't filter by visa sponsorship type, which means most results are irrelevant for Australian nationals seeking E-3 support.
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 Data Analyst role qualify as a specialty occupation for the E-3?
Yes, in most cases. The E-3 specialty occupation standard requires the role to normally require at least a bachelor's degree in a specific field. Clinical Data Analyst positions that involve SAS or R programming, CDISC standards, clinical trial data management, or FDA regulatory submissions consistently meet this threshold. Roles framed as general data entry or basic reporting are less likely to qualify.
How does the E-3 compare to the H-1B for Clinical Data Analysts?
The E-3 is available only to Australian citizens, but that exclusivity works in your favor. There is no annual lottery, no cap that runs out mid-year, and no registration fee tied to random selection. H-1B applicants face a roughly 25 percent selection rate in recent fiscal years. With an E-3, a qualifying job offer and a certified LCA are sufficient to proceed to your consulate interview.
Can I change employers or move to a contract role while on an E-3?
You can change employers, but each new position requires a new LCA certified by the DOL and a new visa stamp reflecting the updated employer details. Contract or staffing agency arrangements are permitted, but the agency must be the petitioning employer and must demonstrate that the placed role meets specialty occupation criteria. Starting the LCA process before your last day at your current employer avoids a gap in authorized employment.
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