eGenesis Visa Sponsorship Jobs USA
eGenesis is a biotechnology company pioneering xenotransplantation research, working to make human-compatible organs from genetically engineered animals. For visa-sponsored scientists and researchers, eGenesis has sponsored H-1B visas and welcomes candidates on F-1 OPT, F-1 CPT, and TN visa status.
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eGenesis is a clinical-stage biotechnology company developing human-compatible engineered organs to address the severe global organ shortage. The Company’s proprietary genome engineering platform enables extensive, multiplex gene edits to remove key biological barriers, add protective human transgenes, and inactivate endogenous retroviruses. EGEN-2784, a genetically engineered porcine kidney, is the Company’s lead program and is currently being evaluated in a multi-patient Expanded Access study at MGH. eGenesis is headquartered in Cambridge, MA.
Position Summary
eGenesis is seeking a resourceful and collaborative Senior Clinical Trial Manager to join our Clinical Operations team to support programs across our portfolio. This role will work closely with our teams across Regulatory, Quality, GMP Production, and Development to successfully drive our clinical programs. As the Senior Clinical Trial Manager, you will be responsible for the day-to-day management of our clinical studies, vendors, and sites in alignment with corporate and program goals. You will work closely with clinical sites and CROs to ensure compliance with SOPs and regulatory guidelines. To be successful in this role, you will leverage a passion for the details, excellent communication skills and an eagerness to collaborate.
Primary Responsibilities
- Assist in overall management of clinical trials, including but not limited to managing study timelines and budgets as well as providing CRO and other external vendor oversight
- Assist in preparation and review of clinical study documentation including, but not limited to, protocol, informed consent, study plans, lab manuals, Case Report Forms, Clinical Study Reports, and other study level documents
- Engage cross-functionally to ensure clear, consistent communication to key stakeholders on study status, metrics and timelines
- Ensure implementation and conduct of study(ies) in accordance with SOPs and ICH-GCP guidelines
- Serve as a point of contact for CRO and clinical site communication
- Assist in the set up the Trial Master File (TMF) and ensure appropriate TMF maintenance throughout the trial, including periodic reviews
- Lead internal study team calls and ensure appropriate cross functional follow up and resolution to tasks in a timely manner
- Participate and coordinate resolution of audit findings and ensure audit-ready condition of clinical trial documentation including central clinical files
- Proactively identify risks in study timelines in regard to key milestones and deliverables and work closely with the cross-functional teams to mitigate downstream impacts
Qualifications
- Bachelor’s degree, life science or medical background preferred
- 7+ years work experience in life sciences or medically related field, including 4+ years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
- Experience in oversight of external vendors (e.g. CROs, central labs, etc.)
- Strong interpersonal and organizational skills are needed, with a high degree of attention to detail with ability to flex communication style to all areas of the organization
- Working knowledge of Good Clinical Practices (GCP) and other relevant regulatory requirements
- Ability to travel up to 10% of the time
- Ability to be onsite in the Cambridge office 2 days per week
Base pay range for this job is $142,800 - $176,400.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
About EGenesis
eGenesis is a clinical-stage biotechnology company developing human-compatible engineered organs to address the severe global organ shortage. The Company’s proprietary genome engineering platform enables extensive, multiplex gene edits to remove key biological barriers, add protective human transgenes, and inactivate endogenous retroviruses. EGEN-2784, a genetically engineered porcine kidney, is the Company’s lead program and is currently being evaluated in a multi-patient Expanded Access study at MGH. eGenesis is headquartered in Cambridge, MA.
Position Summary
eGenesis is seeking a resourceful and collaborative Senior Clinical Trial Manager to join our Clinical Operations team to support programs across our portfolio. This role will work closely with our teams across Regulatory, Quality, GMP Production, and Development to successfully drive our clinical programs. As the Senior Clinical Trial Manager, you will be responsible for the day-to-day management of our clinical studies, vendors, and sites in alignment with corporate and program goals. You will work closely with clinical sites and CROs to ensure compliance with SOPs and regulatory guidelines. To be successful in this role, you will leverage a passion for the details, excellent communication skills and an eagerness to collaborate.
Primary Responsibilities
- Assist in overall management of clinical trials, including but not limited to managing study timelines and budgets as well as providing CRO and other external vendor oversight
- Assist in preparation and review of clinical study documentation including, but not limited to, protocol, informed consent, study plans, lab manuals, Case Report Forms, Clinical Study Reports, and other study level documents
- Engage cross-functionally to ensure clear, consistent communication to key stakeholders on study status, metrics and timelines
- Ensure implementation and conduct of study(ies) in accordance with SOPs and ICH-GCP guidelines
- Serve as a point of contact for CRO and clinical site communication
- Assist in the set up the Trial Master File (TMF) and ensure appropriate TMF maintenance throughout the trial, including periodic reviews
- Lead internal study team calls and ensure appropriate cross functional follow up and resolution to tasks in a timely manner
- Participate and coordinate resolution of audit findings and ensure audit-ready condition of clinical trial documentation including central clinical files
- Proactively identify risks in study timelines in regard to key milestones and deliverables and work closely with the cross-functional teams to mitigate downstream impacts
Qualifications
- Bachelor’s degree, life science or medical background preferred
- 7+ years work experience in life sciences or medically related field, including 4+ years of biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
- Experience in oversight of external vendors (e.g. CROs, central labs, etc.)
- Strong interpersonal and organizational skills are needed, with a high degree of attention to detail with ability to flex communication style to all areas of the organization
- Working knowledge of Good Clinical Practices (GCP) and other relevant regulatory requirements
- Ability to travel up to 10% of the time
- Ability to be onsite in the Cambridge office 2 days per week
Base pay range for this job is $142,800 - $176,400.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
Job Roles at eGenesis
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Get Access To All JobsTips for Finding eGenesis Visa Sponsorship Jobs USA
Target roles that match eGenesis's core research focus
eGenesis works at the intersection of genomics, gene editing, and transplant biology. Scientists and researchers with backgrounds in CRISPR, molecular biology, or immunology align closely with the roles most likely to receive H-1B sponsorship consideration at the company.
Leverage your F-1 OPT or CPT window strategically
eGenesis sponsors F-1 OPT and CPT, making it accessible for international students early in their U.S. career. Starting on OPT gives you time to demonstrate value before the company pursues H-1B sponsorship on your behalf.
Canadian and Mexican candidates have a direct path via TN
eGenesis sponsors TN visas, which don't require a lottery and can often be obtained faster than H-1B. If you're a Canadian or Mexican scientist in a qualifying TN occupation, this can be the most practical entry point.
Highlight specialized technical skills in your application
At a company doing cutting-edge xenotransplantation research, generalist science backgrounds are less competitive. Emphasize domain-specific skills, published research, or lab experience directly relevant to organ engineering, gene editing, or transplant immunology.
Understand that sponsorship reflects genuine hiring need
eGenesis's sponsorship activity reflects focused, specialty hiring rather than high-volume recruiting. Each sponsored role tends to be highly specific, so tailoring your application to the exact research area in the job description significantly improves your chances.
Use Migrate Mate to find and track eGenesis openings
eGenesis doesn't always advertise widely for sponsored roles. Migrate Mate surfaces verified sponsors filtered by visa type and industry, so you can monitor eGenesis openings and apply as soon as a sponsored position in your research area becomes available.
Frequently Asked Questions
Does eGenesis sponsor H-1B visas?
Yes, eGenesis sponsors H-1B visas. The company operates in the Science & Research sector, specifically in xenotransplantation and gene editing, where specialized expertise is often sourced globally. H-1B sponsorship at eGenesis tends to be reserved for roles requiring highly specific scientific qualifications that align with their organ engineering research pipeline.
Which visa types does eGenesis sponsor?
eGenesis sponsors H-1B, F-1 OPT, F-1 CPT, and TN visas. This range covers international students completing degrees in the U.S., early-career researchers on OPT or CPT, Canadian and Mexican professionals eligible for TN status, and experienced scientists requiring H-1B sponsorship. Green Card sponsorship has not been a recent pattern for the company.
Which departments or roles at eGenesis are most likely to receive visa sponsorship?
Sponsorship at eGenesis is concentrated in scientific and research roles. Positions in molecular biology, genomics, immunology, animal science, and translational research are the most likely to be sponsored given the company's focus on developing genetically engineered pig organs for human transplantation. Technical laboratory and research associate positions are also plausible candidates.
How do I apply to eGenesis if I need visa sponsorship?
Start by identifying open roles that match your scientific background on Migrate Mate, which filters employers by verified sponsorship history so you're not wasting time on companies that don't sponsor. When applying to eGenesis, make your visa status clear upfront and emphasize research skills directly relevant to their xenotransplantation work. eGenesis is a focused, specialist employer, so a highly targeted application carries significantly more weight than a general one.
How do I know if eGenesis is actively hiring sponsored roles right now?
eGenesis hiring activity can be sporadic given the company's size and research stage. The best approach is to monitor their open positions consistently rather than applying in a single window. Migrate Mate tracks sponsoring employers and surfaces verified open roles, making it straightforward to stay current on eGenesis postings without manually checking multiple sources.