TN Visa Clinical Data Management Jobs
Clinical Data Management professionals from Canada and Mexico can qualify for TN visa sponsorship under the USMCA as Computer Systems Analysts or Scientists, depending on role scope. Your degree field must align directly with the position. Canadian citizens qualify without a cap; Mexican nationals face a separate allocation process.
See All Clinical Data Management JobsOverview
Showing 5 of 65+ Clinical Data Management jobs
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
Have you applied for this role?
See all 65+ Clinical Data Management jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Data Management roles.
Get Access To All JobsINTRODUCTION
Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer.
ROLE
Senior Director, Clinical Data Management and Analytics, provides leadership to the Clinical Data Management and Analytics Department and provides influence across the Clinical Development organization. As a leader of the Clinical Data Management and Analytics organization, and part of a cross-functional team of drug development scientists focused on providing hands-on skills, expertise, and tools to facilitate strategic development, operational execution, and regulatory compliance to ensure data integrity for clinical trials, in addition to integration, visualization, and exploratory analysis of complex and diverse data in support of clinical development activities and decisions. Through practical hands-on work, the Lead will define approaches, processes, algorithms, and tools that support the analytics, visualizations, and decision support needs of drug development scientists and projects. The Lead will play a key role in building the team with the necessary skills, build relationships with relevant stakeholders, and implement relevant tools and approaches. The Lead will collaborate with Biostatistics leads and other members of drug development teams to ensure connectivity of exploratory analysis work in support of development, regulatory approval, and market acceptance of products. This position includes functional management responsibilities.
Essential Functions and Responsibilities
- Define and implement the overall vision, strategy, and goals for the clinical data management department.
- Lead, manage, and develop data management teams, handling resource planning, staff training, and performance reviews.
- Ensure data integrity, quality, and compliance with regulatory requirements (e.g., FDA, ICH, GCPs) and internal company policies.
- Experience with global trials and regulatory submissions (FDA, EMA).
- Generate novel insights from data and present them via rich and intuitive visualizations.
- Builds successful partnerships and seamless interfaces within the department and the broader research and development organization. Communicates proactively and effectively across several teams with diverse subject matter expertise.
- Ensures quality of deliverables by consistently applying analysis and reporting standards, and driving compliance with regulatory requirements, corporate and departmental SOPs, and work practices.
- Drives the development and implementation of innovative strategies and technologies.
- Independently develops, troubleshoots, and maintains complex programs and utilities in accordance with predefined specifications and build upon existing Iovance standards.
- Provides technical guidance to external partners concerning project and data standards, and analysis practices to ensure efficient and integrated project strategies.
- Identifies opportunities for increased efficiency and consistency within the organization and provides SME support to continuous improvement initiatives.
- Adheres to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics.
- Performs miscellaneous duties as assigned.
BASIC QUALIFICATIONS
- Extensive experience in clinical data management and systems, with proven leadership experience in oncology therapeutic area.
- Proficient knowledge of EDC systems (e.g., Medidata Rave), CDISC standards, and clinical trial processes.
- Drive innovation and continuous process improvement within data management by implementing new technologies and advanced systems to enhance productivity and efficiency.
- Demonstrated ability to lead, motivate, and develop teams.
- Excellent communication and interpersonal skills to effectively collaborate with diverse teams and stakeholders.
- Strong problem-solving and decision-making abilities to resolve complex issues and drive solutions.
- MS, BS/BA degree, or other suitable qualification with relevance to the field.
- 13 or more years’ direct experience in clinical data management in the biotechnology OR Pharmaceutical industry.
- Excellent verbal and written communication skills and strong interpersonal skills are required.
- Demonstrated ability to develop and lead a team of individuals with diverse experience and expertise.
- Ability to explain technically complex information for a non-technical audience.
- Strong positive attitude, thrives in a dynamic, fast paced environment with many simultaneous projects.
- Demonstrates the ability to work within budget constraints, while utilizing resources efficiently and in a fiscally responsible manner.
PREFERRED QUALIFICATIONS
- Experience with AI applications in the data management space is highly desirable.
Physical Demands and Activities Required
- Must be able to remain in a stationary position standing or sitting for prolonged periods of time.
- Must be able to move about inside an office and exert up to 10 pounds of force occasionally or a negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects.
- Must have visual acuity to perform activities such as: preparing and analyzing data and figures, viewing a computer screen, and extensive reading.
- This position requires repetitive motion, substantial movements (motions) of the wrist, hands, and/or fingers.
- Must be able to communicate with others to exchange information.
Mental
Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlines.
Work Environment
This job operates in a professional or remote office environment and requires operating standard office equipment and keyboards.
LI-remote
INTRODUCTION
Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) therapy for people with cancer. We are pioneering a transformational approach to treating cancer by harnessing the ability of the human immune system to recognize and attack diverse cancer cells in each patient. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, which may be a promising option for patients with cancer.
ROLE
Senior Director, Clinical Data Management and Analytics, provides leadership to the Clinical Data Management and Analytics Department and provides influence across the Clinical Development organization. As a leader of the Clinical Data Management and Analytics organization, and part of a cross-functional team of drug development scientists focused on providing hands-on skills, expertise, and tools to facilitate strategic development, operational execution, and regulatory compliance to ensure data integrity for clinical trials, in addition to integration, visualization, and exploratory analysis of complex and diverse data in support of clinical development activities and decisions. Through practical hands-on work, the Lead will define approaches, processes, algorithms, and tools that support the analytics, visualizations, and decision support needs of drug development scientists and projects. The Lead will play a key role in building the team with the necessary skills, build relationships with relevant stakeholders, and implement relevant tools and approaches. The Lead will collaborate with Biostatistics leads and other members of drug development teams to ensure connectivity of exploratory analysis work in support of development, regulatory approval, and market acceptance of products. This position includes functional management responsibilities.
Essential Functions and Responsibilities
- Define and implement the overall vision, strategy, and goals for the clinical data management department.
- Lead, manage, and develop data management teams, handling resource planning, staff training, and performance reviews.
- Ensure data integrity, quality, and compliance with regulatory requirements (e.g., FDA, ICH, GCPs) and internal company policies.
- Experience with global trials and regulatory submissions (FDA, EMA).
- Generate novel insights from data and present them via rich and intuitive visualizations.
- Builds successful partnerships and seamless interfaces within the department and the broader research and development organization. Communicates proactively and effectively across several teams with diverse subject matter expertise.
- Ensures quality of deliverables by consistently applying analysis and reporting standards, and driving compliance with regulatory requirements, corporate and departmental SOPs, and work practices.
- Drives the development and implementation of innovative strategies and technologies.
- Independently develops, troubleshoots, and maintains complex programs and utilities in accordance with predefined specifications and build upon existing Iovance standards.
- Provides technical guidance to external partners concerning project and data standards, and analysis practices to ensure efficient and integrated project strategies.
- Identifies opportunities for increased efficiency and consistency within the organization and provides SME support to continuous improvement initiatives.
- Adheres to Iovance Biotherapeutics’ core values, policies, procedures, and business ethics.
- Performs miscellaneous duties as assigned.
BASIC QUALIFICATIONS
- Extensive experience in clinical data management and systems, with proven leadership experience in oncology therapeutic area.
- Proficient knowledge of EDC systems (e.g., Medidata Rave), CDISC standards, and clinical trial processes.
- Drive innovation and continuous process improvement within data management by implementing new technologies and advanced systems to enhance productivity and efficiency.
- Demonstrated ability to lead, motivate, and develop teams.
- Excellent communication and interpersonal skills to effectively collaborate with diverse teams and stakeholders.
- Strong problem-solving and decision-making abilities to resolve complex issues and drive solutions.
- MS, BS/BA degree, or other suitable qualification with relevance to the field.
- 13 or more years’ direct experience in clinical data management in the biotechnology OR Pharmaceutical industry.
- Excellent verbal and written communication skills and strong interpersonal skills are required.
- Demonstrated ability to develop and lead a team of individuals with diverse experience and expertise.
- Ability to explain technically complex information for a non-technical audience.
- Strong positive attitude, thrives in a dynamic, fast paced environment with many simultaneous projects.
- Demonstrates the ability to work within budget constraints, while utilizing resources efficiently and in a fiscally responsible manner.
PREFERRED QUALIFICATIONS
- Experience with AI applications in the data management space is highly desirable.
Physical Demands and Activities Required
- Must be able to remain in a stationary position standing or sitting for prolonged periods of time.
- Must be able to move about inside an office and exert up to 10 pounds of force occasionally or a negligible amount of force frequently or constantly to lift, carry, push, pull, or otherwise move objects.
- Must have visual acuity to perform activities such as: preparing and analyzing data and figures, viewing a computer screen, and extensive reading.
- This position requires repetitive motion, substantial movements (motions) of the wrist, hands, and/or fingers.
- Must be able to communicate with others to exchange information.
Mental
Clear and conceptual thinking ability; excellent judgment, troubleshooting, problem-solving, analysis, and discretion; ability to handle work-related stress; ability to handle multiple priorities simultaneously; and ability to meet deadlines.
Work Environment
This job operates in a professional or remote office environment and requires operating standard office equipment and keyboards.
LI-remote
See all 65+ Clinical Data Management jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Clinical Data Management roles.
Get Access To All JobsTips for Finding TN Visa Sponsorship as a Clinical Data Management
Verify your degree supports the classification
TN approval for clinical data roles hinges on your degree aligning with the specific USMCA category your employer selects. A life sciences or computer science degree typically works; a general business degree often doesn't, even for data-heavy roles.
Target sponsors with active clinical trial pipelines
Pharma companies, CROs, and academic medical centers running active Phase II or III trials are the employers most likely to need and approve TN sponsorship for CDM roles. Filter your search by therapeutic area and trial phase volume.
Request a specialty occupation letter before accepting
Before signing an offer, ask the employer to draft a support letter confirming the role qualifies as a specialty occupation under USMCA. This document is your front-line defense at the border or consulate, not an afterthought.
Use Migrate Mate to find verified TN-sponsoring employers
Searching broadly wastes time on employers unfamiliar with visa sponsorship. Migrate Mate surfaces Clinical Data Management roles at employers with recent visa filings, so you're targeting companies already experienced with hiring sponsored workers.
Prepare CDISC credentials as supporting evidence
CDISC CDASH or SDTM certifications strengthen your application by demonstrating specialty-level expertise. CBP officers reviewing TN petitions respond well to credentials that distinguish your role from generalist data work.
Confirm your employer's visa sponsorship experience upfront
Your employer prepares a support letter outlining your role and qualifications, which you'll present at the U.S. port of entry (for Canadian citizens) or at a U.S. consulate (for Mexican citizens) to establish your TN status. Ask HR whether they've sponsored work visa candidates before and who manages their immigration compliance.
Clinical Data Management jobs are hiring across the US. Find yours.
Find Clinical Data Management JobsClinical Data Management TN Visa: Frequently Asked Questions
Does Clinical Data Management qualify for TN visa status?
Yes, but the classification depends on how the role is framed. CDM positions typically qualify under the Computer Systems Analyst or Scientist category in the USMCA professional list. Your employer's support letter must describe duties that match the selected category, and your degree must correspond to that field, not just to data or healthcare broadly.
How does TN visa sponsorship compare to H-1B for Clinical Data Management roles?
TN is significantly more accessible for CDM professionals from Canada and Mexico. There's no lottery, no annual cap for Canadians, and approvals can happen at the border in a single day for Canadians. H-1B requires lottery selection, a March registration window, and an October 1 start date. TN status also renews indefinitely in three-year increments, with no maximum duration.
Can Mexican CDM professionals use the TN visa the same way Canadians can?
The USMCA occupational categories are identical, but the process differs. Canadian citizens can apply at a U.S. port of entry directly. Mexican nationals must apply at a U.S. consulate in Mexico and are subject to a separate numerical allocation. Processing timelines and documentation requirements are the same, but Mexican applicants should build consular appointment lead time into their plans.
Where can I find Clinical Data Management jobs with TN visa sponsorship?
Migrate Mate is built specifically for this search. It filters Clinical Data Management roles by employers with TN visa sponsorship history, so you're not guessing which companies will support your status. Searching general platforms surfaces many roles from employers who've never sponsored TN workers and won't know how to start.
What happens to my TN status if my CDM contract ends early?
Your TN status is tied to the specific employer and position listed in your petition. If your contract ends before the approved period expires, you lose TN status authorization. You can accept a new CDM role and apply for a new TN, but you should not work during the gap. Canadians can apply at the border same-day; Mexican nationals need a new consular appointment.
See which Clinical Data Management employers are hiring and sponsoring visas right now.
Search Clinical Data Management Jobs