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Scientific Affairs Manager Jobs (NOW HIRING)

The Associate Director, Scientific Affairs is a self-starter with extensive experience in ... Prefer experience in training, project management and/or staff supervision in a team-based ...

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Scientific Affairs Manager information

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How much do scientific affairs manager jobs pay per hour?

As of May 28, 2026, the average hourly pay for scientific affairs manager in the United States is $45.16, according to ZipRecruiter salary data. Most workers in this role earn between $40.38 and $53.85 per hour, depending on experience, location, and employer.

What Does a Scientific Affairs Manager Do?

As a scientific affairs manager, you oversee informational communications for a medical or scientific research company, such as a pharmaceutical development firm or a scientific professional society. Your responsibilities include maintaining websites and other informational resources about clinical studies, lab news, and research breakthroughs. You may also help develop public education programs, coordinate conferences or other events, and maintain membership databases. In addition to your communications duties, you may seek financial and institutional support for your organization and respond to public inquiries about its research and objectives.

What are the key skills and qualifications needed to thrive as a Scientific Affairs Manager, and why are they important?

To thrive as a Scientific Affairs Manager, you need a strong background in life sciences or a related field, often supported by an advanced degree (e.g., PhD, PharmD) and experience in medical writing or regulatory affairs. Familiarity with regulatory submission systems, scientific literature databases, and compliance standards like GxP is typically required. Excellent communication, project management, and stakeholder engagement skills are vital for collaborating across departments and with external partners. These competencies ensure accurate scientific communication, regulatory compliance, and effective support of product development and commercialization.

How does a Scientific Affairs Manager typically collaborate with cross-functional teams within an organization?

A Scientific Affairs Manager works closely with various departments such as regulatory affairs, clinical development, marketing, and medical affairs to ensure that scientific information is accurately communicated and that product strategies align with scientific evidence. They often serve as the scientific bridge between internal teams and external stakeholders, including healthcare professionals and regulatory agencies. This role involves facilitating knowledge sharing, supporting the development of scientific materials, and ensuring compliance with industry standards. Effective collaboration is key to driving informed decision-making and advancing organizational goals.

What are Scientific Affairs Managers?

Scientific Affairs Managers are professionals responsible for bridging the gap between scientific research and business objectives within organizations, particularly in industries like pharmaceuticals, biotechnology, and healthcare. They oversee scientific communications, manage regulatory compliance, and ensure that products or research findings are accurately and effectively communicated to regulatory bodies, healthcare professionals, and other stakeholders. Their role often involves collaborating with research teams, marketing departments, and regulatory agencies to support the development and approval of new products. Scientific Affairs Managers play a crucial role in ensuring that scientific information is clear, accurate, and aligned with both business goals and regulatory standards.

What is the difference between Scientific Affairs Manager vs Medical Science Liaison?

AspectScientific Affairs ManagerMedical Science Liaison
Required credentialsAdvanced degree (PhD, PharmD, MD)Advanced degree (PhD, PharmD, MD)
Work environmentCorporate, research, and development teamsMedical and clinical settings, healthcare providers
Employer and industry usagePharmaceutical, biotech companiesPharmaceutical, biotech, medical device companies
Common search and comparison intentUnderstanding roles in scientific communication and strategyClarifying clinical and medical information dissemination

The Scientific Affairs Manager and Medical Science Liaison roles both require advanced degrees and work within pharmaceutical and biotech industries. While the Scientific Affairs Manager focuses on strategic scientific communication and regulatory support within companies, the Medical Science Liaison primarily engages with healthcare professionals to share clinical data. Both roles are vital for bridging scientific research and medical practice but differ in their daily interactions and focus areas.

What cities are hiring for Scientific Affairs Manager jobs? Cities with the most Scientific Affairs Manager job openings:
What are the most commonly searched types of Scientific Affairs jobs? The most popular types of Scientific Affairs jobs are:
Who are the top companies hiring for Scientific Affairs Manager jobs? The top employers for Scientific Affairs Manager jobs are:
What states have the most Scientific Affairs Manager jobs? States with the most job openings for Scientific Affairs Manager jobs include:

Regulatory Affairs Manager - APAC - Diabetes Care (on-site)

Abbott

Alameda, CA • On-site

Full-time

Medical, Retirement

Posted 8 days ago


Abbott rating

8.0

Company rating: 8.0 out of 10

Based on 129 frontline employees who took The Breakroom Quiz

131st of 511 rated manufacturers


Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.JOB DESCRIPTION:

Working at Abbott

At Abbott, you can do work that matters, grow, and learn, care for yourself and family, be your true self and live a full life. You'll also have access to:

  • Career development with an international company where you can grow the career you dream of.
  • Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
  • An excellent retirement savings plan with high employer contribution
  • Tuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.
  • A company recognized as a great place to work in dozens of countries around the world and named one of the most admired companies in the world by Fortune.
  • A company that is recognized as one of the best big companies to work for as well as a best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

ThisRegulatory Affairs Manager - APACposition will work on-site at our Alameda, CA location in the Diabetes Care Division. We're focused on helping people with diabetes manage their health with life-changing products that provide accurate data to drive better-informed decisions. We're revolutionizing the way people monitor their glucose levels with our new sensing technology.

ThisRegulatory Affairs Manager - APACposition will work closely with in-country regulatory representatives in the Asia Pacific (APAC) region to ensure efficient and compliant business processes and environment. In this role, you will combine knowledge of scientific, regulatory, and business issues to enable products to meet required legislation in the APAC region. You will be responsible for managing a small team overseeing the Diabetes Care product portfolio in the APAC region, creating robust global regulatory strategies, working with cross-functional teams as the regulatory SME, provide support for compiling regulatory submissions, and ensuring data is effectively presented for the registration of products in the APAC region.

What You'll Work On

  • Managing a team of regulatory specialists
  • Develop and advance the organizations policy and procedures for regulatory affairs and compliance to establish a compliant culture.
  • Represent Regulatory Affairs on cross-functional project teams and provide strategic input and technical guidance on regulatory requirements in the APAC region for Diabetes care's projects.
  • Utilize technical regulatory skills to propose strategies on complex issues
  • Work closely with in-country regulatory representatives, compile, prepare, and review medical device or IVD submissions to regulatory agencies in the APAC region.
  • Provide strategic input and technical guidance on regulatory authority queries.
  • Evaluate proposed design and manufacturing changes for regulatory impact and implement required regulatory actions.
  • Anticipate regulatory and related obstacles and emerging issues throughout the product lifecycle.
  • Oversee processes involved with maintaining annual licenses, registrations, listings and patent information.
  • Ensure compliance with product post marketing approval requirements
  • Review product labeling and promotional materials to ensure compliance with relevant regulatory requirements.
  • Provide regulatory support for internal and external audits.

Required Qualifications

  • Bachelor's Degree OR an equivalent combination of education and experience.
  • 4-5 years' experience in a regulated industry (e.g., medical products, nutritionals). 2-5 years of experience in regulatory preferred but may consider quality assurance, research and development/support, scientific affairs, operations, or related area.
  • Strong verbal and written communications with ability to effectively communicate and present at multiple levels in the organization.

Preferred Qualifications

  • Bachelor's Degree in science (biology, chemistry, microbiology, immunology, medical technology, pharmacy, pharmacology), math, engineering, or medical fields.
  • Masters in technical area or MBA; PhD in a technical are or law.
  • 5+ years' experience in regulatory affairs.
  • Supervisory experience.
  • Scientific writing experience.
  • Working knowledge of ISO and EN standards, as well as country-specific standards in the APAC region.
  • Strong working knowledge of regulatory requirements for the APAC region.
  • Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society).

Apply Now

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com

Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.

Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.Connect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.

The base pay for this position is

$114,000.00 - $228,000.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:Regulatory OperationsDIVISION:ADC Diabetes CareLOCATION:United States > Alameda : 1360-1380 South Loop RoadADDITIONAL LOCATIONS:WORK SHIFT:StandardTRAVEL:Yes, 20 % of the TimeMEDICAL SURVEILLANCE:NoSIGNIFICANT WORK ACTIVITIES:Awkward/forceful/repetitive (arms above shoulder, bent wrists), Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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