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Msc Medical Biotechnology Jobs (NOW HIRING)

Head of Regulatory Affairs (Boston)

Boston, MA · On-site

$163K - $215K/yr

... within biotech, pharma, or CRO environments. * Advanced degree (MSc or PhD) strongly preferred ... The company offers a competitive package, including medical insurance, vision insurance, and 401(k) ...

Candidates with an MSc or equivalent postgraduate scientific degree will be considered with an ... or biotechnology organizations. Additional Information #LI-MK1 #LI-Hybrid Our Commitment to ...

Candidates with an MSc or equivalent postgraduate scientific degree will be considered with an ... or biotechnology organizations. Additional Information #LI-MK1 #LI-Hybrid Our Commitment to ...

Candidates with an MSc or equivalent postgraduate scientific degree will be considered with an ... or biotechnology organizations. Additional Information #LI-MK1 #LI-Hybrid Our Commitment to ...

Principal Medical Writer

Durham, NC · On-site

$84 - $211/hr

... g., MSc, PhD, PharmD, MD) preferred. * Minimum of 7+ years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or ...

$84 - $211/hr

... g., MSc, PhD, PharmD, MD) preferred. * Minimum of 7+ years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or ...

New

... g., MSc, PhD, PharmD, MD) preferred * Minimum of 7+ years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or ...

NY · On-site

$52 - $76/hr

MSc in Life Sciences (e.g., Biotechnology, Molecular Biology, or related) * Solid laboratory ... Our benefits include private medical care and an on-site gym I consent to the processing of my ...

... g., MSc, PhD, PharmD, MD) preferred * Minimum of 7+ years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or ...

... g., MSc, PhD, PharmD, MD) preferred * Minimum of 7 + years of experience in medical writing within the biopharmaceutical, biotechnology, or CRO industry; equivalent experience in clinical or ...

... MPH, MSc, or equivalent experience preferred * 6+ years of publications, medical affairs, or medical communications experience within an agency, pharmaceutical, biotech, academic, or related ...

Medical Strategist

Philadelphia, PA · Hybrid

$122K - $158K/yr

MSc or similar postgraduate scientific degree. * 7+ years of relevant experience in medical strategy, medical communications, pharma/biotech, or related fields. * Strong analytical skills with the ...

$180 - $320/hr

... or MSc with 5+ years of pharmaceutical and biotechnology experience * Strong foundation in DMPK ... care (Medical, Dental, Vision) * Opportunity to work at the forefront of cancer research in a ...

Reporting to the Chief Medical Officer (CMO), the Sr. Director will play a critical leadership role ... Advanced degree (PhD, PharmD, MD, or MSc) in life sciences or related field. * Minimum 8+ years of ...

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Msc Medical Biotechnology information

See salary details

$36.5K

$164.7K

$337K

How much do msc medical biotechnology jobs pay per year?

As of Sep 5, 2026, the average yearly pay for 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 is an MSc in Medical Biotechnology?

An MSc in Medical Biotechnology is a postgraduate degree focused on the application of biological and technological principles to the field of medicine. This program covers topics such as genetic engineering, drug development, molecular biology, and diagnostics, preparing graduates for roles in research, pharmaceuticals, healthcare, and biotechnology industries. Students gain both theoretical knowledge and hands-on laboratory experience, enabling them to contribute to advancements in medical science and healthcare solutions. Graduates may pursue careers in research institutions, biotech companies, hospitals, or continue with doctoral studies.

What types of teams and professionals do MSc Medical Biotechnology graduates typically collaborate with in their roles?

Graduates with an MSc in Medical Biotechnology often work in multidisciplinary teams that may include molecular biologists, clinical researchers, bioinformaticians, and physicians. Collaboration is key, especially in research and development settings or clinical laboratories, where each member contributes specialized expertise to advance projects, such as developing new diagnostic tools or therapies. This teamwork fosters a dynamic environment, encourages knowledge sharing, and provides opportunities to learn from other experts, helping to build a strong foundation for career growth and innovation.

What are the key skills and qualifications needed to thrive as an MSc Medical Biotechnology professional, and why are they important?

To thrive as an MSc Medical Biotechnology professional, you need a solid background in molecular biology, genetics, and biochemistry, typically supported by a master's degree in medical biotechnology or a related field. Familiarity with laboratory technologies such as PCR, cell culture, bioinformatics software, and regulatory compliance standards is essential. Critical thinking, problem-solving, and strong collaboration skills help professionals innovate and work effectively in multidisciplinary research or clinical teams. These competencies are crucial for advancing biomedical research, developing new therapies, and ensuring accurate and ethical application of biotechnological solutions.

What is the difference between Msc Medical Biotechnology vs Msc Biotechnology?

AspectMsc Medical BiotechnologyMsc Biotechnology
FocusMedical applications, drug development, diagnosticsIndustrial, agricultural, environmental applications
Work EnvironmentHospitals, biotech firms, research labsBiotech companies, research institutions, agriculture
Required SkillsCell culture, molecular biology, clinical researchGenetic engineering, fermentation, product development

While both degrees involve biotechnology, Msc Medical Biotechnology emphasizes medical and clinical applications, working closely with healthcare and diagnostics. Msc Biotechnology has a broader scope, including industrial and environmental uses. The choice depends on your career focus—medical or general biotech industries.

Is MSc Medical Biotechnology a good career?

MSc Medical Biotechnology is a promising career path involving research, development, and application of biotechnological techniques in healthcare. Graduates can work in pharmaceuticals, diagnostics, or research labs, often requiring knowledge of molecular biology, lab skills, and regulatory standards. The field offers opportunities for advancement and specialization, making it a valuable option for those interested in biomedical sciences.

What jobs can you get with a Master of Science in Medical Biotechnology?

A Master of Science in Medical Biotechnology prepares graduates for roles such as biomedical scientist, research associate, clinical research coordinator, quality control analyst, or regulatory affairs specialist. These positions often require knowledge of laboratory techniques, data analysis, and regulatory standards, and may involve working in laboratories, research institutions, or pharmaceutical companies.
More about Msc Medical Biotechnology jobs

What cities are hiring for Msc Medical Biotechnology jobs?

Cities with the most Msc Medical Biotechnology job openings:

What are the most commonly searched types of Msc Medical Biotechnology jobs?

The most popular types of Msc Medical Biotechnology jobs are:

Infographic showing various Msc Medical Biotechnology job openings in the United States as of August 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $164,731 per year, or $79.2 per hour.

[Voronoi, Inc.] Medical Writer (Hybrid Work)

VORONOI, Inc.

Cambridge, MA • On-site

$110 - $170/hr

Other

Posted 17 days ago


Job description

[Voronoi, Inc.] Medical Writer (Hybrid Work)

Medical Writer - Oncology Clinical Trials

Location: minimum 2 days onsite in Waltham, MA office Cambridge / Greater Boston

Position Summary:

We are seeking an experienced Medical Writer with a strong background in oncology clinical trials to join our growing company. The ideal candidate will have a deep understanding of oncology therapeutic areas and a proven track record of preparing high-quality regulatory and scientific documents in support of clinical development programs.

Key Responsibilities:
  • Develop, write, and edit clinical and regulatory documents related to oncology clinical trials, including but not limited to:
  • Clinical study protocols and amendments
  • Investigator brochures
  • Clinical study reports (CSRs)
  • Informed consent forms
  • Briefing documents
  • Clinical sections of INDs, NDAs, BLAs, and other regulatory submissions
  • Collaborate with cross-functional teams including Clinical Development, Regulatory Affairs, Biostatistics, Data Management, and Safety teams to ensure content accuracy and consistency
  • Interpret and synthesize complex clinical and scientific data into clear, concise, and scientifically sound documents
  • Ensure all documents comply with ICH guidelines, regulatory requirements, and internal SOPs
  • Participate in strategic planning and document timelines
  • Mentor junior medical writers or contractors as needed
  • Stay current with therapeutic area developments, industry trends, and regulatory guidance
Qualifications:
  • Advanced degree (PhD, PharmD, MD, or MSc) in life sciences, medicine, or a related field
  • Minimum 5 years of medical writing experience, with at least 3 years focused on oncology clinical trials
  • In-depth understanding of oncology disease areas and clinical endpoints
  • Extensive experience in authoring documents for Phase I–III oncology trials and regulatory submissions
  • Strong knowledge of ICH-GCP, FDA/EMA guidelines, and clinical trial processes
  • Excellent written and verbal communication skills
  • High attention to detail, strong analytical skills, and ability to manage multiple projects under tight deadlines
  • Proficiency with document management systems and MS Office Suite; experience with templates and style guides
Preferred Qualifications:
  • Experience working in a CRO, biotech, or pharmaceutical company
  • Familiarity with submission processes (eCTD) and regulatory publishing
  • Membership in professional organizations such as AMWA or EMWA is preferred
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