Systimmune Visa Sponsorship USA
Systimmune is a clinical-stage biopharmaceutical company developing next-generation antibody-based therapies. It sponsors H-1B and F-1 OPT visas, making it a viable target for international candidates in oncology, immunology, and related scientific disciplines looking to build a U.S.-based career in biotech.
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Get Access To All JobsINTRODUCTION
SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
ROLE AND RESPONSIBILITIES
SystImmune is seeking a high quality, ambitious and experienced Clinical Trial Assistant to support day-to-day operations of SystImmune clinical studies. Assisting and providing support to the members of the clinical operations project team to facilitate the management clinical trial processes including planning, execution, and closeout of outsourced clinical trials. You will ensure that the trial is conducted in compliance with the protocol, ICH good clinical practice, applicable regulatory requirements, and applicable standard operating procedure work instructions.
Responsibilities:
- Develop and distribute meeting agendas, minutes and monthly status reports to document key project updates and communications to relevant stakeholders, as requested.
- Participate in regular team meeting / teleconferences; CRO, Vendor and Investigator Site meetings as necessary; and Investigator Meetings, as necessary.
- Support Clinical Project Management team in communication to CRO, Vendors and Investigator Sites.
- Support the Clinical Project Management team with study start-up activities, to include preparing and/or reviewing study-related documents (e.g., Monitoring Plan, Laboratory Manual, Clinical Site Procedures Manual, Pharmacy Manual, and CRF Completion Guidelines, study logs and forms Site Contracts and Budgets, Vendor Contracts and Budgets, etc.).
- Support the Clinical Project Management team in the tracking of subject recruitment at all study sites; monitoring visits and approval; infringements, breaches, and misconduct, fraud, and negative trends and protocol deviations. Notify CRO and sites of updates on global study information.
- Assist Clinical Project Management team in the collection, review and filing of site Essential Documents, and maintenance of the TMF.
- Assist in the tracking of clinical supplies at site in coordination with established systems such as IWRS, EDC and CTMS as needed.
- Support the Clinical Project Management team in formal risk assessment activities; review and corrective action plans across study, participates in the planning of quality assurance activities, internal and external audits/inspections, and coordinates communication of audit/inspection findings.
- Communication and support Clinical Project Management team with cross-functional study team interaction.
- Perform other duties as assigned.
BASIC QUALIFICATIONS
- Bachelor’s degree in health science or related field.
- 2 years in research experience preferred.
- Excellent verbal and written communication skills required.
- Excellent organizational, multi-tasking and time management skills required.
- Working knowledge of International Conference on Harmonization Good Clinical Practice guidelines.
- Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF).
- Located in NJ or can commute to Princeton, NJ.
- Ability to travel as required.
COMPENSATION AND BENEFITS
The expected base salary range for this position is $60,000 - $90,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
EEO STATEMENT
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
INTRODUCTION
SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials, SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discovery and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
ROLE AND RESPONSIBILITIES
SystImmune is seeking a high quality, ambitious and experienced Clinical Trial Assistant to support day-to-day operations of SystImmune clinical studies. Assisting and providing support to the members of the clinical operations project team to facilitate the management clinical trial processes including planning, execution, and closeout of outsourced clinical trials. You will ensure that the trial is conducted in compliance with the protocol, ICH good clinical practice, applicable regulatory requirements, and applicable standard operating procedure work instructions.
Responsibilities:
- Develop and distribute meeting agendas, minutes and monthly status reports to document key project updates and communications to relevant stakeholders, as requested.
- Participate in regular team meeting / teleconferences; CRO, Vendor and Investigator Site meetings as necessary; and Investigator Meetings, as necessary.
- Support Clinical Project Management team in communication to CRO, Vendors and Investigator Sites.
- Support the Clinical Project Management team with study start-up activities, to include preparing and/or reviewing study-related documents (e.g., Monitoring Plan, Laboratory Manual, Clinical Site Procedures Manual, Pharmacy Manual, and CRF Completion Guidelines, study logs and forms Site Contracts and Budgets, Vendor Contracts and Budgets, etc.).
- Support the Clinical Project Management team in the tracking of subject recruitment at all study sites; monitoring visits and approval; infringements, breaches, and misconduct, fraud, and negative trends and protocol deviations. Notify CRO and sites of updates on global study information.
- Assist Clinical Project Management team in the collection, review and filing of site Essential Documents, and maintenance of the TMF.
- Assist in the tracking of clinical supplies at site in coordination with established systems such as IWRS, EDC and CTMS as needed.
- Support the Clinical Project Management team in formal risk assessment activities; review and corrective action plans across study, participates in the planning of quality assurance activities, internal and external audits/inspections, and coordinates communication of audit/inspection findings.
- Communication and support Clinical Project Management team with cross-functional study team interaction.
- Perform other duties as assigned.
BASIC QUALIFICATIONS
- Bachelor’s degree in health science or related field.
- 2 years in research experience preferred.
- Excellent verbal and written communication skills required.
- Excellent organizational, multi-tasking and time management skills required.
- Working knowledge of International Conference on Harmonization Good Clinical Practice guidelines.
- Experienced in Microsoft Office Products (Word, Excel, PowerPoint, SharePoint, Teams) and other clinical trial systems (e.g., CTMS, EDC and eTMF).
- Located in NJ or can commute to Princeton, NJ.
- Ability to travel as required.
COMPENSATION AND BENEFITS
The expected base salary range for this position is $60,000 - $90,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.
EEO STATEMENT
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
Job Roles at Systimmune Companies
How to Get Visa Sponsorship in Systimmune Visa Sponsorship USA
Target roles that align with Systimmune's core science
Systimmune's work centers on antibody-drug conjugates and bispecific antibodies. Roles in molecular biology, protein engineering, and clinical development are most likely to attract sponsorship consideration. Tailor your application to reflect direct experience in these therapeutic areas.
Position yourself for H-1B sponsorship early in the process
Systimmune sponsors H-1B visas, so research and scientific roles with clear degree requirements are strong candidates for sponsorship. Make sure your qualifications map directly to the specialty occupation standard before you apply.
Reach out through scientific and clinical networks
Clinical-stage biotechs like Systimmune hire selectively. Connections through oncology conferences, academic collaborations, or biotech industry groups can surface opportunities before they're widely posted. Warm introductions carry more weight at smaller organizations than cold applications.
Time your application around clinical development milestones
Hiring at clinical-stage companies often accelerates around trial phases or pipeline expansions. Monitoring Systimmune's clinical announcements can signal when teams are growing. Browse verified sponsors on Migrate Mate to track sponsorship-active companies in the same biotech space.
Be specific about your visa status and timeline upfront
Smaller biotechs appreciate candidates who are transparent about sponsorship needs and timelines from the first conversation. Clearly stating your current status, OPT expiration, and H-1B eligibility reduces friction and demonstrates preparation, qualities that matter in a focused scientific organization.
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Get Access To All JobsFrequently Asked Questions
Does Systimmune sponsor H-1B visas?
Yes, Systimmune sponsors H-1B visas. The company has an active sponsorship track record, primarily supporting scientific and research-oriented roles that meet the specialty occupation requirement. If you're targeting an H-1B with Systimmune, focus your application on positions with clear degree requirements in life sciences, biopharmaceutical development, or related technical fields.
What visa types does Systimmune sponsor?
Systimmune sponsors H-1B and F-1 OPT visas. The H-1B pathway suits candidates in specialty scientific and technical roles, while F-1 OPT sponsorship makes Systimmune accessible to recent graduates still within their post-degree work authorization window. At this time, the company does not have a documented track record of Green Card or E-3 sponsorship.
Which departments or roles at Systimmune are most likely to receive visa sponsorship?
Given Systimmune's focus on antibody-drug conjugates and immuno-oncology, roles in research and development, preclinical and clinical sciences, regulatory affairs, and bioanalytical functions are the most likely candidates for sponsorship. Positions requiring specialized graduate-level training in biology, chemistry, or pharmaceutical sciences align best with the H-1B specialty occupation standard that Systimmune applies.
How do I find open visa-sponsored jobs at Systimmune?
Migrate Mate surfaces verified visa-sponsoring companies so you can filter opportunities by real sponsorship history rather than guessing from job postings. Search for Systimmune directly on Migrate Mate to see current openings and confirm active sponsorship status before investing time in an application. This is especially useful if your timeline is tight and you need confirmed sponsors quickly.
How do I approach the application timeline when targeting Systimmune for H-1B sponsorship?
The H-1B cap lottery runs once a year, with registrations typically opening in March for an October 1 start date. If you're already on F-1 OPT, you may be able to begin work at Systimmune while your H-1B petition is pending. Start conversations with the hiring team well in advance of the registration window, ideally three to four months before March, so both sides have time to align on the petition process.
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