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Freelance Pharmaceutical Regulatory Affairs Jobs in Utah

Varsity Tutors

Biomedical Engineering Tutor

Provo, UT · Remote

$40/hr

... and regulatory affairs. Ability to explain signal processing for biosignals, finite element ... and pharmaceutical development. * Curriculum Awareness & Adaptive Instruction: Familiar with ...

Varsity Tutors

Biomedical Engineering Tutor

Logan, UT · Remote

$40/hr

... and regulatory affairs. Ability to explain signal processing for biosignals, finite element ... and pharmaceutical development. * Curriculum Awareness & Adaptive Instruction: Familiar with ...

Takeda

Plasma Center Nurse- RN

Layton, UT

$33.44/hr

BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. About the role: Every ... The Medical Support Specialist will be familiar with regulations of the plasma collection industry ...

Takeda

Plasma Center Nurse- LPN

Layton, UT

$24.32 - $33.44/hr

BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. About the role: Every ... The Medical Support Specialist will be familiar with regulations of the plasma collection industry ...

Takeda

Paramedic/EMT-P

Layton, UT

$24.32 - $33.44/hr

BioLife Plasma Services is a subsidiary of Takeda Pharmaceutical Company Ltd. About the role: Every ... The Medical Support Specialist will be familiar with regulations of the plasma collection industry ...

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Freelance Pharmaceutical Regulatory Affairs information

What are the key skills and qualifications needed to thrive as a Freelance Pharmaceutical Regulatory Affairs professional, and why are they important?

To thrive as a Freelance Pharmaceutical Regulatory Affairs professional, a strong background in regulatory guidelines, pharmaceutical sciences, and compliance—often supported by a relevant degree and regulatory certifications such as RAC—is essential. Expertise with regulatory submission platforms (e.g., eCTD), document management systems, and familiarity with global regulatory databases is highly valued. Outstanding attention to detail, effective communication, and project management skills distinguish top performers in this field. These competencies ensure timely, accurate submissions and ongoing compliance in a dynamic regulatory environment, which is critical for product approvals and business success.

What are some common challenges faced by freelance pharmaceutical regulatory affairs professionals, and how can they be managed?

Freelance pharmaceutical regulatory affairs professionals often face challenges such as staying updated with constantly evolving regulations across multiple markets, managing workload fluctuations, and ensuring clear communication with diverse clients. To effectively manage these challenges, freelancers should invest in ongoing professional development, utilize regulatory databases and networks, and establish clear project scopes and timelines from the outset. Building strong relationships with clients and maintaining organized documentation also help ensure projects run smoothly and meet compliance requirements.

What are freelance pharmaceutical regulatory affairs professionals?

Freelance pharmaceutical regulatory affairs professionals are independent experts who help pharmaceutical companies navigate and comply with regulations governing drug development, approval, and marketing. They often assist with preparing and submitting documentation to regulatory agencies, ensuring products meet legal and safety standards. These freelancers may work with multiple clients on a project basis, providing specialized knowledge in areas such as clinical trial submissions, labeling, and post-market surveillance. Their expertise helps companies bring products to market efficiently while minimizing regulatory risks.

What is the difference between Freelance Pharmaceutical Regulatory Affairs vs Pharmaceutical Regulatory Affairs Specialist?

AspectFreelance Pharmaceutical Regulatory AffairsPharmaceutical Regulatory Affairs Specialist
CredentialsTypically requires relevant degrees and certifications; flexible credentials based on client needsUsually requires a degree in pharmacy, life sciences, or related field, with certifications preferred
Work EnvironmentIndependent, remote, project-basedEmployed by companies or agencies, often in office settings
Employer & Industry UsageFreelance consultants serve multiple clients across pharma and biotechFull-time or part-time employees within pharmaceutical companies or regulatory agencies

Freelance Pharmaceutical Regulatory Affairs professionals offer flexible, project-based services to various clients, while Pharmaceutical Regulatory Affairs Specialists are typically employed full-time within organizations. Both roles require relevant credentials, but freelancers often work independently across multiple projects, whereas specialists are embedded within companies to ensure regulatory compliance.

What are the most commonly searched types of Pharmaceutical Regulatory Affairs jobs in Utah? The most popular types of Pharmaceutical Regulatory Affairs jobs in Utah are:
What are popular job titles related to Freelance Pharmaceutical Regulatory Affairs jobs in Utah? For Freelance Pharmaceutical Regulatory Affairs jobs in Utah, the most frequently searched job titles are:
What job categories do people searching Freelance Pharmaceutical Regulatory Affairs jobs in Utah look for? The top searched job categories for Freelance Pharmaceutical Regulatory Affairs jobs in Utah are:
What cities in Utah are hiring for Freelance Pharmaceutical Regulatory Affairs jobs? Cities in Utah with the most Freelance Pharmaceutical Regulatory Affairs job openings:
Freelance Pharmaceutical Regulatory Affairs jobs near you

State Government Affairs Director

Biomerieux

Salt Lake City, UT • On-site

$154.80K - $193.50K/yr

Full-time

Medical, Dental, Vision, Life, Retirement

Posted 15 days ago

Job description

Description
Position Summary
The State Government Affairs Director will report to the Vice President of Government Affairs. This individual is responsible for representing bioMérieux before US State policymakers, political organizations and related stakeholders and will implement long-term plans for all State legislative and Medicaid advocacy work in prioritized states. This position collaborates with the internal and external matrix organization to identify and pursue areas of mutual opportunity with States based on policy and legislative opportunities for bioMérieux's diagnostic tests in clinical applications including respiratory, GI and women's health.
Primary Duties
  • Lead the US State Government Affairs initiatives to protect and advance patient access to bioMérieux diagnostics and its business units before policymakers, elected officials, trade and business associations as well as other allies and influencers.
  • Build the reputation of bioMérieux US State Government Affairs as the preferred, go-to trusted partner, honest brokers who drive for constructive solutions.
  • Establish and maintain relationships with key members of State government agencies and executive offices.
  • Involved in identifying key targets, prioritizing resources, networking with office staffs and developing outreach and grassroots programs.
  • Stay apprised of business goals and strategies in order to assess impact to bioMérieux from state/regional, executive and regulatory activities.
  • Identify health care, economic and other State policy developments that could impact bioMérieux's business and operations including environmental, R&D, and human resources.
  • Represent bioMérieux with key state-level political organizations including: NCSL, CSG, NCOIL.
  • Actively participate in key product launches to ensure state-level perspectives.
  • Perform all work in compliance with company quality procedures and standards.
  • Perform other duties as assigned.

    • Qualifications
    Required Education, Training and Experience
    • Bachelor degree in public administration, public health, health administration, political science, life sciences, business or other related field.
    • 7+ years of professional related experience that may include any of the following or a combination thereof:
      • Experience lobbying multiple states on issues such as regulation, funding/reimbursement, access programs or related topics.
      • Experience as a state-level legislative staffer or congressional aide.
      • Experience as a state-government affairs lobbyist
    • In lieu of a Bachelor's degree, 4 years of additional relevant experience, defined above, will be accepted.

    Preferred Education, Training and Experience
    • Advanced degree in Public Administration, Public Health or Health Administration or other related field.
    • Experience managing multiple contract state lobbyists.
    • Experience lobbying multiple states for healthcare (pharmaceutical, vaccines or medical devices).
    • Prior involvement with government agencies at the state-level.
    • Established network of contacts within government and with third-party consultants and lobbyists particularly in the healthcare sector.

    Knowledge, Skills, and Abilities
    • Consistently upholds and reflects the core ethical principles and values that bioMérieux promotes.
    • Effective Presentation Skills - including the ability to present technical data.
    • Ability to deal with difficult situations in a timely and bold manner.
    • Creativity in forming new ideas, solutions, and approaches to challenges; to think outside-the-box.
    • Leading without authority through influence and guidance of others towards a common goal by using expertise, persuasion, and personal qualities to inspire action.
    • Effectively navigate social interactions in the workplace.
    • Skilled in MS Office tools to include but not limited to Outlook, Teams, Word, and Excel.
    • Advanced: demonstrates deep knowledge; manages complex tasks and integrates multiple tools independently.
    • Extensive experience and understanding of US state-level political environment (e.g., budget process, rulemaking and Medicaid).
    • Knowledge of state legislative and rulemaking processes; experience researching and analyzing complex public policy issues.
    • Extensive policy and analytical expertise with the ability to drive consensus among a diverse array of interests and priorities.

    Working Conditions and Physical Requirements
    • Ability to remain in stationary position, either sitting or standing, for prolonged periods
    • Ability to ascend/descend stairs, ladders, ramps, and the like

    Travel Requirements
    • Domestic travel required: 40% of time
    • International travel required: 5% of time

    The estimated salary range for this field-based role is between $154,800 - $193,500. This role is eligible to receive a variable annual bonus based on company, team, and individual performance per bioMerieux's bonus program. This range may differ from ranges offered for similar positions elsewhere in the country given differences in cost of living. Actual compensation within this range is determined based on the successful candidate's experience and will be presented in writing at the time of the offer.
    In addition, bioMérieux offers a competitive Total Rewards package that may include:
    • A choice of medical (including prescription), dental, and vision plans providing nationwide coverage and telemedicine options
    • Company-Provided Life and Accidental Death Insurance
    • Short and Long-Term Disability Insurance
    • Retirement Plan including a generous non-discretionary employer contribution and employer match.
    • Adoption Assistance
    • Wellness Programs
    • Employee Assistance Program
    • Commuter Benefits
    • Various voluntary benefit offerings
    • Discount programs
    • Parental leaves

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