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Biotechnology Content Writing Jobs (NOW HIRING)

Travere

Senior Manager, Medical Writing

San Diego, CA · On-site +1

... ready content. * Ensure adherence to applicable FDA, EMA, ICH, and other relevant regulatory ... within the biotechnology, pharmaceutical, CRO, or related healthcare industry environment.

Ambition 24Hours Inc

Senior Medical Writer

The Lakes, NV · Remote

$142K - $195K/yr

... writing experience within biotech, pharmaceutical, or CRO environments Extensive experience ... regulatory content rather than editing or project management Demonstrated excellence in CSR ...

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Biotechnology Content Writing information

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How much do biotechnology content writing jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for biotechnology content writing in the United States is $40.46, according to ZipRecruiter salary data. Most workers in this role earn between $23.56 and $46.39 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Biotechnology Content Writing position, and why are they important?

To excel in Biotechnology Content Writing, you need a strong background in life sciences, excellent writing and research abilities, and often a degree in biotechnology, biology, or a related field. Familiarity with content management systems (CMS), citation software, and sometimes certifications in scientific communication or technical writing are highly valued. Attention to detail, critical thinking, and the ability to communicate complex scientific concepts to both technical and non-technical audiences are essential soft skills. These competencies enable you to create accurate, engaging content that supports marketing, education, or regulatory goals in the biotech sector.

What does a typical workday look like for someone in Biotechnology Content Writing?

A typical day for a Biotechnology Content Writer involves researching the latest developments in biotechnology, writing and editing articles, white papers, or web content, and collaborating closely with scientists, marketers, and editors. You may attend team meetings to align content strategy, review feedback on previous work, and ensure accuracy through fact-checking and sourcing credible references. Deadlines are a regular part of the role, so strong time management is important. Many positions offer opportunities to specialize in areas such as medical devices, pharmaceuticals, or emerging biotech fields, which can lead to career advancement and subject matter expertise.

What is a Biotechnology Content Writing job?

A Biotechnology Content Writing job involves creating informative, accurate, and engaging content related to biotechnology, such as scientific articles, blog posts, whitepapers, and marketing materials. Writers in this field translate complex scientific concepts into accessible language for researchers, professionals, and the general public. They may work for biotech companies, research institutions, healthcare firms, or science publications. Strong research skills, scientific knowledge, and the ability to write clearly are essential for success in this role.

More about Biotechnology Content Writing jobs
What cities are hiring for Biotechnology Content Writing jobs? Cities with the most Biotechnology Content Writing job openings:
What are the most commonly searched types of Biotechnology Content Writing jobs? The most popular types of Biotechnology Content Writing jobs are:
What states have the most Biotechnology Content Writing jobs? States with the most job openings for Biotechnology Content Writing jobs include:
What job categories do people searching Biotechnology Content Writing jobs look for? The top searched job categories for Biotechnology Content Writing jobs are:
Biotechnology Content Writing jobs near you
Infographic showing various Biotechnology Content Writing job openings in the United States as of July 2026, with employment types broken down into 6% Internship, 80% Full Time, 11% Part Time, 1% Temporary, and 2% Contract. Highlights an 75% Physical, 2% Hybrid, and 23% Remote job distribution, with an average salary of $84,151 per year, or $40.5 per hour.
Associate Director, Medical Affairs Operations

Associate Director, Medical Affairs Operations

Vir Biotechnology

San Francisco, CA • On-site

$176K - $246K/yr

Other

Medical, Retirement, PTO

Posted 4 days ago

New

Job description

THE OPPORTUNITY

Vir Biotechnology is seeking an Associate Director, Medical Affairs Operations to support the execution and advancement of Medical Affairs capabilities across key functional areas. This individual will play a critical role in enabling Medical Affairs activities by driving operational excellence, strengthening cross-functional alignment, and ensuring efficient and compliant execution of programs.

This role will partner closely within Medical Affairs and cross-functional stakeholders to operationalize strategic initiatives, support launch readiness, and enhance the infrastructure required to deliver high-quality Medical Affairs activities.

In addition to core operational responsibilities, this role will contribute to Medical Affairs initiatives beyond traditional operations, including support for scientific materials, review processes, and cross-functional content execution. The successful candidate will be expected to flex across operational and Medical Affairs activities as needed to support emerging priorities and new initiatives, ensure continuity of execution, and drive overall impact.

This position reports to the Vice President, Medical Affairs.

This role is based at our San Francisco headquarters, with an expectation of at least three days per week in the office.

WHAT YOU'LL DO
  • Drive cross-functional coordination across Medical Affairs, Clinical Development, Commercial, and external partners to enable delivery of key programs and initiatives
  • Lead the identification, implementation, and optimization of Medical Affairs processes, systems, and governance frameworks, including the establishment of new capabilities as needed
  • Partner with Medical, Legal, Compliance, and other stakeholders to ensure compliant execution of external engagements, content use, and Medical Affairs activities
  • Support the development, review, and execution of Medical Affairs materials and programs (e.g., MSL resources, scientific presentations, congresses, advisory boards, and medical information capabilities)
  • Coordinate and execute Medical Affairs activities, including congress planning, advisory boards, external presentations, and medical information capabilities (including program setup and ongoing operations)
  • Manage vendor and partner relationships across the full lifecycle, including contracting, execution, and delivery of Medical Affairs programs
  • Contribute to Medical Affairs budgeting, forecasting, and financial tracking in collaboration with Finance and leadership
  • Drive adoption and effective use of systems and tools (e.g., CRM, content and data platforms), and support tracking, reporting, and insights generation
  • Maintain audit-ready processes across Medical Affairs activities, ensuring alignment with internal policies and regulatory requirements
  • Support additional Medical Affairs operational and programmatic activities as needed to ensure continuity of execution, including areas such as publication and authorship operations, establishment and management of medical information workflows, content review coordination, and management of select vendors, systems, and internal infrastructure
  • Coordinate activities of the MARC and SRC including but not limited to (1) creating the agenda, (2) assigning unique identifier number to each submission, (3) scheduling weekly meetings, (4) ensuring all materials are submitted and reviewed in accordance with this SOP, (5) documenting meeting discussions, (6) tracking materials from initial submission, MARC review, and final approval by VPMA , (7) ensuring documentation of reviews and final approval, (8) administering the documentation tracking system, (8) training new participants on this MARC SOP and other MARC ways of working.
WHO YOU ARE AND WHAT YOU BRING
  • Advanced degree (PharmD, PhD, or equivalent) preferred with 7+ years of relevant experience
  • Significant experience in Medical Affairs, Medical Affairs Operations, or a related function within the pharmaceutical or biotechnology industry
  • Demonstrated ability to operate effectively and independently in a cross-functional, matrixed environment and manage complex initiatives
  • Experience with operational processes such as content review, contracting, budgeting, or vendor management
  • Strong organizational skills with the ability to manage multiple priorities in a fast-paced environment
  • Excellent written and verbal communication skills, with the ability to engage effectively across stakeholders
  • Experience supporting Medical Information, Field Medical (MSL), or Scientific Communications activities preferred
  • Familiarity with systems used in Medical Affairs (e.g., CRM, content management, reporting tools) preferred
  • Understanding of applicable regulatory and compliance frameworks (e.g., PhRMA, FDA, or regional equivalents) preferred
#LI-AS1
#LI-Onsite
 
WHO WE ARE AND WHAT WE OFFER

The expected salary range for this position is $176,500 to $246,500 per year. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors.

Vir Biotechnology's compensation and benefits are aligned with the current market and commensurate with the person's experience and qualifications. All full-time employees receive a package that includes compensation, bonus and equity as well as many other Vir Biotechnology benefits and perks such as health and welfare benefit plans, non-accrual paid time off, company shut down for holidays, commuter benefits, 401K match and lunch each day in the office.

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