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Remote Msc Medical Biotechnology Jobs (NOW HIRING)

Ambition 24Hours Inc

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

Fully Remote (U.S.) Industry: Pharmaceutical / Biotechnology Employment Type: Full-Time Salary ... Medical Writer to support clinical development and regulatory documentation activities within a ...

Danaher

Business Development Manager

Oakland, CA · On-site +1

$145K - $175K/yr

Identify, prospect and close new business opportunities in biotech, pharma, academic and government ... MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ...

Danaher

Business Development Manager

Palo Alto, CA · On-site +1

$145K - $175K/yr

Identify, prospect and close new business opportunities in biotech, pharma, academic and government ... MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ...

Danaher

Business Development Manager

Fremont, CA · On-site +1

$145K - $175K/yr

Identify, prospect and close new business opportunities in biotech, pharma, academic and government ... MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ...

Danaher

Business Development Manager

Sunnyvale, CA · On-site +1

$145K - $175K/yr

Identify, prospect and close new business opportunities in biotech, pharma, academic and government ... MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ...

Danaher

Business Development Manager

San Francisco, CA · On-site +1

$145K - $175K/yr

Identify, prospect and close new business opportunities in biotech, pharma, academic and government ... MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ...

Danaher

Business Development Manager

Boston, MA · On-site +1

$145K - $175K/yr

MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ... We recognize the benefits of flexible, remote working arrangements for eligible roles and are ...

Danaher

Business Development Manager

San Jose, CA · On-site +1

$145K - $175K/yr

Identify, prospect and close new business opportunities in biotech, pharma, academic and government ... MSc, PhD or MBA * Supporting early or late-stage clinical programs and/or GMP manufacturing ...

YO AI Labs

Clinical Document Author - Remote

Houston, TX · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Location: Remote Job Type: Contractor Pay: $50-$80/hour ... Advanced degree in Life Sciences, Pharmacy, Medicine, or a related field (MD, PharmD, PhD, or MSc)

New

YO AI Labs

Clinical Document Author - Remote

San Jose, CA · Remote

$50 - $80/hr

Medical Writer / Clinical Document Author Location: Remote Job Type: Contractor Pay: $50-$80/hour ... Advanced degree in Life Sciences, Pharmacy, Medicine, or a related field (MD, PharmD, PhD, or MSc)

New

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Remote Msc Medical Biotechnology information

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$36.5K

$164.7K

$337K

How much do remote msc medical biotechnology jobs pay per year?

As of Aug 14, 2026, the average yearly pay for remote msc medical biotechnology in the United States is $164,731.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,000.00 and $268,500.00 per year, depending on experience, location, and employer.

What are some common challenges faced by professionals working remotely in MSc Medical Biotechnology roles, and how can they be addressed?

Remote MSc Medical Biotechnology professionals often face challenges such as limited hands-on laboratory access, coordinating effectively with research teams across time zones, and maintaining engagement in collaborative projects. These can be addressed by utilizing virtual laboratory simulations, regularly scheduled video meetings, and clear communication tools to stay connected with colleagues. Additionally, proactively seeking mentorship and participating in online seminars or workshops can help remote professionals stay updated with industry trends and foster career development.

What are the key skills and qualifications needed to thrive as a remote MSc Medical Biotechnology professional?

To excel as a Remote MSc Medical Biotechnology professional, you need a strong background in molecular biology, genetics, and biotechnology, typically evidenced by an MSc degree in a relevant field. Experience with laboratory techniques, bioinformatics tools, and data analysis software such as PCR, ELISA, and programs like BLAST or Python is frequently required. Excellent written communication, problem-solving, and self-motivation are vital soft skills, especially when collaborating virtually with research teams. These abilities ensure accurate scientific work, effective remote teamwork, and continued contribution to advancing medical biotechnology.

What are remote MSc Medical Biotechnology programs?

Remote MSc Medical Biotechnology programs are graduate-level courses that can be completed primarily online, allowing students to study biotechnology concepts and techniques from anywhere. These programs cover subjects such as molecular biology, genetic engineering, and clinical research, often including virtual labs and remote projects. The flexibility of remote study makes it accessible for working professionals or international students who cannot attend in-person classes. Graduates are equipped for careers in pharmaceuticals, research, diagnostics, or further academic study.

What is the difference between Remote Msc Medical Biotechnology vs Remote Msc Biomedical Research Assistant?

AspectRemote Msc Medical BiotechnologyRemote Msc Biomedical Research Assistant
Required CredentialsMaster's in Medical Biotechnology or related fieldMaster's in Biomedical Sciences or related field
Work EnvironmentLaboratory, research facilities, or remote data analysisResearch labs, clinical settings, or remote research support
Employer & Industry UsageBiotech companies, research institutions, pharmaHospitals, research institutes, biotech firms

Both roles often require a master's degree in a related field and involve research, but Medical Biotechnology focuses on developing medical products and therapies, while Biomedical Research Assistants support various research projects across biomedical sciences. The roles overlap in skills and work environment, but differ in specific focus areas within the industry.

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Remote Msc Medical Biotechnology jobs near you
Infographic showing various Remote Msc Medical Biotechnology job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, and 6% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $164,731 per year, or $79.2 per hour.

Principal Regulatory Writer (Temporary)

Vir Biotechnology

Remote

$180 - $200/hr

Temporary

Re-posted 20 days ago

Job description

Vir Biotechnology, Inc. is a clinical-stage biopharmaceutical company focused on powering the immune system to transform lives by discovering and developing medicines for serious infectious diseases and cancer. Its clinical-stage portfolio includes programs for chronic hepatitis delta and multiple PRO-XTEN® dual-masked T-cell engagers across validated targets in solid tumor indications. Vir Biotechnology also has a preclinical portfolio of programs across a range of infectious diseases and oncologic malignancies.
Vir Biotechnology has exclusive rights to the universal PRO-XTEN® masking platform for oncology and infectious disease. PRO-XTEN® is a trademark of Amunix Pharmaceuticals, Inc., a Sanofi company.
We believe the success of our colleagues drives the success of our mission. We are committed to creating a company where everyone feels supported and encouraged to give their best.
THE OPPORTUNITY
Vir Biotechnology is looking for a Principal Regulatory Writer (Temporary) who will support all aspects of regulatory submissions writing needs. You will collaborate with senior management and other leads to support consistent documents/messaging within and across programs.
This Person will report to the Senior Director, Regulatory Writing.
WHAT YOU'LL DO
  • Craft clear, accurate, and compliant documents required for regulatory submissions to global health authorities including FDA and EMA
  • Write and edit a wide range of regulatory documents, including but not limited to: Clinical trial protocols and amendments, Investigator Brochures (IBs), Clinical Study Reports (CSRs), briefing packages, internal/external facing labeling documents (eg, CCDS/CCSI, annotated draft labels, IFU, patient leaflets, etc), and components of regulatory submission dossiers (eg, NDA, IND, MAA) such as Module 2 and 5 summary documents (eg, SCS, SCE, ISS, etc)
  • Ensure that all written materials strictly adhere to regulatory guidelines, industry standards, and internal quality standards
  • Analyze complex scientific and medical information, including clinical trial data, translating it into clear, concise, and accurate language understandable by both technical and non-technical audiences
  • Work closely with cross-functional teams (eg, clinical research and operations, biostatistics, regulatory affairs, pharmacology, safety, etc) to ensure comprehensive and accurate document content
  • Manage medical writing projects, including developing timelines (working with the study/project teams, as necessary) and communication with cross-functional team members to maintain awareness of review cycles and expectations
  • Participate in cross-functional meetings to provide input regarding medical writing deliverables, timelines, and any process(es) needed for the completion of regulatory documents
  • Participate in defining and writing standard operating procedures and best practices for efficient preparation of quality documents
  • Provide teams with guidance about best practices and industry standards, offer solutions to authoring hurdles, support interaction and understanding across functional areas

WHO YOU ARE AND WHAT YOU BRING
  • Bachelor's and 15 to 20 years of relevant experience required. Advanced degree in science or medical field is a plus
  • Experience with all common study-level and submission-level regulatory documents such as CSRs, IBs, DSURs, protocols, and eCTD modules required
  • Proven experience with marketing applications (INDs, BLAs, NDAs, MAAs, or equivalents) including responses to health authorities, 90/120-day safety updates, or other post-submission activities required
  • Expert understanding of eCTD structure and the clinical development process, and in-depth knowledge of document-related ICH guidelines and GxPs
  • Proven ability to manage complex projects and influence cross-functional teams

#LI-AS1
#LI-Remote
WHO WE ARE AND WHAT WE OFFER
The expected hourly range for this position is $180.00 to $200.00. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.
Applicants must currently be authorized to work for any employer in the U.S. We are unable to sponsor or take over sponsorship of an employment Visa at this time.
All employment decisions at Vir Biotechnology are based on legitimate, non-discriminatory business requirements, job duties and individual qualifications. Employment decisions are made without regard to any legally protected characteristics.
This commitment extends to all management practices and decisions, including recruitment and hiring, compensation, appraisal systems, promotions, training and career development programs. Vir Biotechnology also strongly commits to providing employees with a work environment free of unlawful conduct or harassment.
Vir Biotechnology Human Resources leads recruitment and employment for Vir Biotechnology. Unsolicited resumes sent to the company from recruiters do not constitute any type of relationship between the recruiter and Vir Biotechnology and do not obligate us to pay fees should we hire from those resumes. We ask that external recruiters and/or agencies not contact or present candidates directly to our hiring manager or employees.
For hires based in the United States, Vir Biotechnology, participates in E-Verify.
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