Green Card Medical Writer Jobs
Medical Writer roles at pharmaceutical, biotech, and CRO employers qualify for EB-2 or EB-3 green card sponsorship through PERM labor certification, which requires employers to document recruitment efforts before filing your I-140 petition. Advanced-degree candidates with regulatory writing experience often qualify at the EB-2 level, unlocking faster priority dates for many nationalities.
Find Green Card Medical Writer JobsOverview
Showing 5 of 52+ Medical Writer jobs
See all 52+ Medical Writer Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Medical Writer roles.
Get Access To All JobsINTRODUCTION
MannKind Corporation is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient‑centric solutions, developing and commercializing innovative inhaled therapeutics and drug‑device technologies aimed at addressing serious unmet needs across endocrine, cardiorenal, and orphan lung diseases. The company applies deep expertise in formulation science and inhalation‑device engineering to reduce the treatment burden for conditions such as diabetes, congestive heart failure, pulmonary fibrosis, and pulmonary hypertension.
MannKind’s core technologies, including ultrafine dry‑powder formulations and advanced inhalation platforms, enable rapid, convenient delivery of medicines directly to the deep lung. This approach supports both local pulmonary targeting and systemic delivery for various medical indications. Through alternative drug formulations and delivery mechanisms, MannKind aims to bring forward differentiated, patient‑centric therapies that expand treatment options to improve outcomes across chronic and rare diseases.
At MannKind, our employees are our greatest asset. We foster a close-knit, collaborative culture where every team member plays a vital role in our mission. We are proud to champion a rich blend of backgrounds, perspectives, and working styles as we work together to improve health outcomes and change lives.
Position Summary:
MannKind Corporation is seeking a detail-oriented and highly organized Medical Writer to join our team. The Medical Writer will provide advanced scientific writing expertise and ensure the successful preparation of high-quality documents including but not limited to study protocols, CSRs, DSURS, IB, safety narratives, publications and submission documents. This role involves providing medical writing support for multiple compounds and projects within multiple therapeutic areas, potentially interfacing with external groups, and serving as the scientific writing expert for the department.
Essential Duties and Job Functions:
- Coordinate and lead the review, approval, and production of writing projects, arranging and driving review meetings with cross-functional teams.
- Ensure effective communication among project team members and contributors, holding them accountable to agreed-upon project dates.
- Leads strategic document preparation for INDs, NDAs and briefing documents.
- Establish best practices, workflow infrastructure/templates, and standards to enhance consistency and quality across all regulatory and scientific documents.
- Oversee the development and finalization of high-quality, scientifically accurate, ICH-compliant documents, including clinical study protocols and reports, Investigator Brochures, Periodic Safety Updates, patient narratives, and manuscripts for peer-reviewed publications.
- Stay abreast of global regulatory requirements and guidelines (FDA, EMA, PMDA, ICH, etc.), ensuring company compliance and best practices.
- Partner with cross-functional teams, including clinical development, medical affairs, regulatory affairs, safety to ensure seamless integration of medical writing.
- Lead and oversee medical writing project timelines, ensuring alignment with broader corporate milestones.
- Serve as the medical writer representative on project teams.
- Write and edit scientific, clinical, or abstracts, posters, presentations, digital enhancements, and manuscripts aligned with scientific narrative and objectives.
- Complete reviews, quality checks and approvals.
- Summarize results presented in graphical, tabular, and/or listing format.
- Interpret complex clinical data and convert it into clear, concise, and engaging scientific content for diverse audiences.
Knowledge, Experience and Skills:
- BS/BA +12 / MS/MBA 8-10, PhD 5+
- Degree in science or medical related field. Master’s or PhD preferred.
- Minimum of 7 years relevant industry experience in medical writing in sponsor/CRO setting or academia, or related areas such as quality, regulatory submissions, publications, clinical research, or product support/R&D.
- Knowledge of US and international regulations, requirements, and guidance associated with writing projects.
- Excellent written and oral communication skills, attention to detail, and ability to correct errors in spelling, punctuation, grammar, consistency, clarity, and accuracy.
- Extensive experience working with collaborative, cross-functional teams.
- Develop and/or update document templates, work instructions, style guides, and department-related processes (SOPs).
- Experience working on publications for multiple therapeutic areas, endocrinology and pulmonology preferred.
- Understanding of publication/scientific communication guidelines.
- Ability to provide strategic oversight while managing multiple priorities in a fast-paced environment.
- Deep understanding of ICH-GCP guidelines and other relevant regulatory requirements.
- Strategic thinker with strong execution skills.
LI-Remote
LI-Onsite
INTRODUCTION
MannKind Corporation is a biopharmaceutical company dedicated to transforming chronic disease care through innovative, patient‑centric solutions, developing and commercializing innovative inhaled therapeutics and drug‑device technologies aimed at addressing serious unmet needs across endocrine, cardiorenal, and orphan lung diseases. The company applies deep expertise in formulation science and inhalation‑device engineering to reduce the treatment burden for conditions such as diabetes, congestive heart failure, pulmonary fibrosis, and pulmonary hypertension.
MannKind’s core technologies, including ultrafine dry‑powder formulations and advanced inhalation platforms, enable rapid, convenient delivery of medicines directly to the deep lung. This approach supports both local pulmonary targeting and systemic delivery for various medical indications. Through alternative drug formulations and delivery mechanisms, MannKind aims to bring forward differentiated, patient‑centric therapies that expand treatment options to improve outcomes across chronic and rare diseases.
At MannKind, our employees are our greatest asset. We foster a close-knit, collaborative culture where every team member plays a vital role in our mission. We are proud to champion a rich blend of backgrounds, perspectives, and working styles as we work together to improve health outcomes and change lives.
Position Summary:
MannKind Corporation is seeking a detail-oriented and highly organized Medical Writer to join our team. The Medical Writer will provide advanced scientific writing expertise and ensure the successful preparation of high-quality documents including but not limited to study protocols, CSRs, DSURS, IB, safety narratives, publications and submission documents. This role involves providing medical writing support for multiple compounds and projects within multiple therapeutic areas, potentially interfacing with external groups, and serving as the scientific writing expert for the department.
Essential Duties and Job Functions:
- Coordinate and lead the review, approval, and production of writing projects, arranging and driving review meetings with cross-functional teams.
- Ensure effective communication among project team members and contributors, holding them accountable to agreed-upon project dates.
- Leads strategic document preparation for INDs, NDAs and briefing documents.
- Establish best practices, workflow infrastructure/templates, and standards to enhance consistency and quality across all regulatory and scientific documents.
- Oversee the development and finalization of high-quality, scientifically accurate, ICH-compliant documents, including clinical study protocols and reports, Investigator Brochures, Periodic Safety Updates, patient narratives, and manuscripts for peer-reviewed publications.
- Stay abreast of global regulatory requirements and guidelines (FDA, EMA, PMDA, ICH, etc.), ensuring company compliance and best practices.
- Partner with cross-functional teams, including clinical development, medical affairs, regulatory affairs, safety to ensure seamless integration of medical writing.
- Lead and oversee medical writing project timelines, ensuring alignment with broader corporate milestones.
- Serve as the medical writer representative on project teams.
- Write and edit scientific, clinical, or abstracts, posters, presentations, digital enhancements, and manuscripts aligned with scientific narrative and objectives.
- Complete reviews, quality checks and approvals.
- Summarize results presented in graphical, tabular, and/or listing format.
- Interpret complex clinical data and convert it into clear, concise, and engaging scientific content for diverse audiences.
Knowledge, Experience and Skills:
- BS/BA +12 / MS/MBA 8-10, PhD 5+
- Degree in science or medical related field. Master’s or PhD preferred.
- Minimum of 7 years relevant industry experience in medical writing in sponsor/CRO setting or academia, or related areas such as quality, regulatory submissions, publications, clinical research, or product support/R&D.
- Knowledge of US and international regulations, requirements, and guidance associated with writing projects.
- Excellent written and oral communication skills, attention to detail, and ability to correct errors in spelling, punctuation, grammar, consistency, clarity, and accuracy.
- Extensive experience working with collaborative, cross-functional teams.
- Develop and/or update document templates, work instructions, style guides, and department-related processes (SOPs).
- Experience working on publications for multiple therapeutic areas, endocrinology and pulmonology preferred.
- Understanding of publication/scientific communication guidelines.
- Ability to provide strategic oversight while managing multiple priorities in a fast-paced environment.
- Deep understanding of ICH-GCP guidelines and other relevant regulatory requirements.
- Strategic thinker with strong execution skills.
LI-Remote
LI-Onsite
See all 52+ Green Card Medical Writer Jobs
Sign up for free to unlock all listings, filter by visa type, and get alerts for new Green Card Medical Writer Jobs.
Get Access To All JobsTips for Finding Green Card Sponsorship as a Medical Writer
Align your credentials to EB-2 requirements
EB-2 requires an advanced degree or its equivalent in a relevant field like life sciences, pharmacy, or communications. If your master's is from outside the U.S., get a credential evaluation completed before targeting roles, since PERM audits often scrutinize foreign degree equivalencies.
Target employers with active PERM filing history
Pharmaceutical companies, contract research organizations, and medical device firms regularly sponsor Medical Writers through PERM. Use Migrate Mate to filter employers by green card filing activity, so you're applying to companies that have already run the PERM recruitment process for this role.
Understand how the PERM recruitment window affects your timeline
Employers must advertise the Medical Writer role through DOL-mandated recruitment steps before filing your PERM application. This process typically takes four to six months before your I-140 petition is even submitted, so negotiate your start date and any relocation plans around that window.
Verify your salary offer meets DOL prevailing wage
Before accepting an offer, check the wage level for your specific Medical Writer job title and work location using the OFLC Wage Search. PERM applications are rejected if the offered wage falls below the DOL-certified prevailing wage, and renegotiating after filing is not possible.
Ask employers whether EB-2 or EB-3 fits your background
Some employers default to EB-3 for Medical Writers even when candidates qualify for EB-2. If your role requires an advanced degree and your background supports it, ask your employer's immigration counsel to evaluate both options, since EB-2 carries priority date advantages for most nationalities.
Distinguish PERM sponsorship from H-1B when negotiating
Unlike H-1B visa, PERM-based green card sponsorship is permanent and not subject to an annual lottery. Employers bear most filing costs and must demonstrate no qualified U.S. workers are available, so come prepared to explain your specialized regulatory or clinical writing background during the offer conversation.
Green Card Medical Writer: Frequently Asked Questions
Do Medical Writer roles typically qualify for EB-2 or EB-3 green card sponsorship?
Medical Writer positions most often qualify under EB-2 when the role requires an advanced degree in a life science, pharmacy, or related field, or under EB-3 when a bachelor's degree meets the minimum requirement. The classification depends on what the employer documents as the actual minimum requirement for the specific position during the PERM process, not just the candidate's own credentials.
How does PERM green card sponsorship differ from H-1B for a Medical Writer?
PERM sponsorship leads to permanent residency rather than temporary status, and it isn't subject to an annual lottery or numerical cap at the EB-3 level for most nationalities. The tradeoff is time: PERM labor certification, followed by I-140 filing and adjustment of status, typically takes two to four years or more depending on your country of birth and USCIS processing queues, compared to H-1B approval in a few months.
What documentation should a foreign Medical Writer prepare before applying for sponsored roles?
You'll need academic transcripts and a foreign credential evaluation if your degree is from outside the U.S., a detailed employment history showing relevant regulatory or clinical writing experience, and copies of any published work or submission documents that demonstrate your technical writing scope. Employers and their immigration counsel use this documentation to establish your qualifications during the PERM recruitment and I-140 filing stages.
How can I find Medical Writer employers that sponsor green cards?
Search Migrate Mate to identify pharmaceutical, biotech, CRO, and medical device companies with documented green card sponsorship history for Medical Writer or related roles. Focusing your applications on employers who have completed PERM filings before significantly reduces the risk of an employer declining to sponsor mid-process due to unfamiliarity with the requirements.
Can my employer sponsor me for a green card if I'm currently on an H-1B as a Medical Writer?
Yes. Employers can initiate PERM labor certification while you remain in valid H-1B status, and you can extend your H-1B beyond the standard six-year cap under AC21 rules once your I-140 is approved and your priority date is more than 365 days old. USCIS allows concurrent H-1B extensions and pending adjustment of status applications, so your work authorization remains uninterrupted during the green card process.