Systimmune Visa Sponsorship Jobs USA
Systimmune is a clinical-stage biopharmaceutical company developing next-generation antibody-based therapies. It sponsors H-1B visa 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 Bothell, 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
The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams, external partners, and vendors to design, configure, and test clinical database systems, conduct data review, and support company deliverables. The CDM will support and/or lead clinical database design, data collection and validation, data management, and reporting work for clinical trials. Additionally, the CDM will play a key role in overseeing CROs and vendors to meet study needs and deliverables.
This position requires you to be Hybrid (3 days required onsite) in Princeton, NJ.
Responsibilities:
- Leads all DM lifecycle activities, from study start-up, maintenance, database lock and close-out.
- Independently develop DM documents including but not limited to Data Management Plans (DMP), Case Report Forms (CRFs), CRF Completion Guidelines, Edit Checks, UAT specifications, centralized monitoring plans, data flow and integrity plans, blinding plans, and data review plans. Utilize templates and standard guidelines to initiate documents, but demonstrate critical thinking, alignment-building and discretion to tailor documents to study needs.
- Independently lead data cleaning activities such as, but not limited to, study team data reviews, Non-system Edit Check Output review, SAE reconciliation, and non-CRF data reconciliation. Gather cross-functional input to drive creation of custom data review plans. Evaluate options and exercise discretion to choose efficient and effective issues resolution paths.
- Manage data deliverables processes and database locks, with high quality and efficiency.
- Foster collaboration and relationship-building with all study team representatives (e.g. Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project Managers, Clinical Trial Managers, CRAs, Clinical Pharmacologists, Biomarker/Bioinformatics Scientists, Medical Writers, Regulatory representatives, etc.)
- DM Project Management: With oversight, ensure data management deliverables are met on time. Utilize communication, available metrics reports, experience, knowledge, and other resources to efficiently lead and coordinate all data management activities. Ensure study team members from different functional areas understand and deliver components affecting data to ensure successful execution of deliverables. Provide solutions for data management issues that arise during study conduct.
- Manage/coordinate work performed by vendors/CROs as appropriate to ensure quality of product. Assist in the selection of vendors/CROs (e.g. review RFPs, attend site audits).
- Performs Medical Coding as needed, works with CROs, Medical Monitors, and Clinical Scientists to coordinate activities for the medical review of clinical trial data.
- Run SAS and/or R programs, review SAS and/or R logs, troubleshoot errors, and generate output. Program SAS and/or R Non-System Edit Checks/Back-end checks and SAS and/or R Data Listings as appropriate for skill level.
- Evaluate CDM processes and applications for improvements; participate in working groups to develop and implement new processes and applications.
- Participate in development of DM specific SOPs.
- Responsible for oversight of CRO data management activities and integrating the various functional group input.
- All other duties as assigned.
QUALIFICATIONS
- BA or BS and a minimum of 4 years of relevant experience.
- Technologically savvy; quickly picks-up new information, standards, regulations, tools, methods or software as it relates to position and profession.
- Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC).
- SAS programming experience.
- Experience with managing Lab Data, such as PK, PD, and Biomarkers.
- Detail-oriented; performs quality and accurate work.
- Knowledgeable in GCP standards, CDISC standards (CDASH, SDTM, ADaM), FDA and ICH guidelines, and GCDMP.
- Strong knowledge of clinical research, drug development process, and medical terminology, oncology experience preferred.
- Knowledge and understanding of DM Lifecycle associated with P1-P3 studies, including pivotal, blinded, and randomized trials.
- Knowledge of MedDRA and WHO Drug coding.
- Project Management skills, ability to manage multiple projects and meet deadlines.
- Strong interpersonal, organizational, and communication skills.
- Prior experience writing specification documents and/or work instructions.
- Previous vendor/CRO management.
- Previous experience with RTSM, eCOA/ePRO systems.
Compensation and Benefits:
The expected base salary range for this position is $100,000 - $170,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
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.
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 Bothell, 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
The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams, external partners, and vendors to design, configure, and test clinical database systems, conduct data review, and support company deliverables. The CDM will support and/or lead clinical database design, data collection and validation, data management, and reporting work for clinical trials. Additionally, the CDM will play a key role in overseeing CROs and vendors to meet study needs and deliverables.
This position requires you to be Hybrid (3 days required onsite) in Princeton, NJ.
Responsibilities:
- Leads all DM lifecycle activities, from study start-up, maintenance, database lock and close-out.
- Independently develop DM documents including but not limited to Data Management Plans (DMP), Case Report Forms (CRFs), CRF Completion Guidelines, Edit Checks, UAT specifications, centralized monitoring plans, data flow and integrity plans, blinding plans, and data review plans. Utilize templates and standard guidelines to initiate documents, but demonstrate critical thinking, alignment-building and discretion to tailor documents to study needs.
- Independently lead data cleaning activities such as, but not limited to, study team data reviews, Non-system Edit Check Output review, SAE reconciliation, and non-CRF data reconciliation. Gather cross-functional input to drive creation of custom data review plans. Evaluate options and exercise discretion to choose efficient and effective issues resolution paths.
- Manage data deliverables processes and database locks, with high quality and efficiency.
- Foster collaboration and relationship-building with all study team representatives (e.g. Biostatisticians, Statistical Programmers, Medical Monitors, Clinical Scientists, Clinical Project Managers, Clinical Trial Managers, CRAs, Clinical Pharmacologists, Biomarker/Bioinformatics Scientists, Medical Writers, Regulatory representatives, etc.)
- DM Project Management: With oversight, ensure data management deliverables are met on time. Utilize communication, available metrics reports, experience, knowledge, and other resources to efficiently lead and coordinate all data management activities. Ensure study team members from different functional areas understand and deliver components affecting data to ensure successful execution of deliverables. Provide solutions for data management issues that arise during study conduct.
- Manage/coordinate work performed by vendors/CROs as appropriate to ensure quality of product. Assist in the selection of vendors/CROs (e.g. review RFPs, attend site audits).
- Performs Medical Coding as needed, works with CROs, Medical Monitors, and Clinical Scientists to coordinate activities for the medical review of clinical trial data.
- Run SAS and/or R programs, review SAS and/or R logs, troubleshoot errors, and generate output. Program SAS and/or R Non-System Edit Checks/Back-end checks and SAS and/or R Data Listings as appropriate for skill level.
- Evaluate CDM processes and applications for improvements; participate in working groups to develop and implement new processes and applications.
- Participate in development of DM specific SOPs.
- Responsible for oversight of CRO data management activities and integrating the various functional group input.
- All other duties as assigned.
QUALIFICATIONS
- BA or BS and a minimum of 4 years of relevant experience.
- Technologically savvy; quickly picks-up new information, standards, regulations, tools, methods or software as it relates to position and profession.
- Experience working within a Clinical EDC system (e.g., Medidata Rave, Veeva EDC).
- SAS programming experience.
- Experience with managing Lab Data, such as PK, PD, and Biomarkers.
- Detail-oriented; performs quality and accurate work.
- Knowledgeable in GCP standards, CDISC standards (CDASH, SDTM, ADaM), FDA and ICH guidelines, and GCDMP.
- Strong knowledge of clinical research, drug development process, and medical terminology, oncology experience preferred.
- Knowledge and understanding of DM Lifecycle associated with P1-P3 studies, including pivotal, blinded, and randomized trials.
- Knowledge of MedDRA and WHO Drug coding.
- Project Management skills, ability to manage multiple projects and meet deadlines.
- Strong interpersonal, organizational, and communication skills.
- Prior experience writing specification documents and/or work instructions.
- Previous vendor/CRO management.
- Previous experience with RTSM, eCOA/ePRO systems.
Compensation and Benefits:
The expected base salary range for this position is $100,000 - $170,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s qualifications, experience, and skills.
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.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.
Job Roles at Systimmune
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Get Access To All JobsTips for Finding Systimmune Visa Sponsorship Jobs 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.
Understand F-1 OPT sponsorship before applying
Systimmune sponsors F-1 OPT, which means recent graduates can enter without immediate H-1B sponsorship. If your OPT window is active, lead with that flexibility, it lowers the barrier for a smaller biotech weighing sponsorship costs and timelines.
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.
Frequently 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 visa 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.