Senior Medical & Scientific Advisor - LCMS

Kentucky Bar Association; United States; Remote; USD 113,000 - 190,000; Full time

Job summary

IQVIA Laboratories seeks a Senior Medical and Scientific Advisor for a remote position to provide comprehensive scientific and technical advice in drug development. This role involves collaboration with stakeholders globally and requires extensive experience in clinical trials, particularly around bioanalytical immunoassay methodologies. Join us to support innovation in healthcare and make impactful contributions to patient outcomes.

Qualifications

• B.S. diploma required; M.S. or Ph.D. preferred.
• Minimum of 10 years experience in pharmaceutical or clinical trial environment.
• Experience with immunoassay is essential.

Responsibilities

• Serve as primary scientific point of contact and provide oversight.
• Ensure engagement between bioanalytical and clinical scientists.
• Support feasibility discussions for assay transfer and validation.
• Drive evaluation of new technologies and technical approaches.
• Coordinate scientific activities across Q2 Solutions laboratories.

Skills

Knowledge of LCMS

GXP laboratory regulations

Scientific and technical knowledge for clinical testing

Bioanalytical immunoassay knowledge

Organizational skills

Willingness to travel

Education

B.S. diploma

M.S. and/or Ph.D. diploma

Job description

We are seeking a Senior Medical and Scientific Advisor to join IQVIA Laboratories in a remote position.

We hire passionate innovators who drive healthcare forward through thoughtful and inclusive collaboration. If you want to discover a career with greater purpose, join us as we transform and accelerate research and development.

As a Senior Medical and Scientific Advisor, you will be providing scientific and technical advice to guide and make recommendations on bioanalytical strategy with key internal and external stakeholders to support drug development programs. You will be ensuring these align with internal capabilities and coordinate with technical, scientific support, and sales functions across the Americas, Europe, Asia Pacific, and China Labs. This position is based in the US, supporting both US and global drug development programs.

What you’ll be doing:

• Serving as the primary scientific point of contact and provide global scientific oversight for key stakeholders.
• Ensuring early engagement between bioanalytical scientists and clinical scientists to provide input on assays, platforms, and associated technical aspects of testing.
• Supporting feasibility discussions concerning assay transfer and validation to ensure bioanalytical methods fit study requirements and regulatory compliance.
• Driving evaluation of new technology and technical approaches to support our sponsors.
• Performing research, benchmarking, and comparative analyses to nurture innovation and review new technologies/assays and areas of opportunity for potential assay development.
• Coordinating scientific activities across Q2 Solutions bioanalytical laboratories, Q2 Solutions lab network, and scientific advisors (e.g., oncology, anatomic pathology, genomics, immunoassays, flow cytometry, and CDx/IVD, regulatory).
• Participating in laboratory investigations and be responsible for scientific escalation.
• Contributing to scientific governance meetings.
• Utilizing the extended capabilities of our parent organizations, IQVIA and Quest Diagnostics, for disease area and other subject matter expertise.
• Providing scientific/technical support for bid defense prep meetings and capability presentations.
• Supporting scientifically sound approaches/proposals for bid teams for RFIs, RFPs, and other queries related to clinical trials.
• Working with internal functions (e.g., marketing, strategy) to help create scientific client-facing material (e.g., slide decks, webinars, newsletters, web content) and representing Q2 Solutions at conferences and other events.
• Utilizing sound knowledge and understanding of Q2 Solutions internal processes, practices, and capabilities.
  

What We Are Looking For:

• B.S. diploma is a minimal requirement.
• A minimum of 10 years of experience in the pharmaceutical or clinical trial environment, including experience with immunoassay.
• M.S. and/or Ph.D. diploma is preferred.
• Other equivalent combinations of education, training, and experience may be accepted in lieu of a degree.
  

The Knowledge, Skills, and Abilities needed for this role:

• Strong knowledge/experience with LCMS.
• General knowledge of GXP laboratory regulations.
• Sound scientific and technical knowledge as it relates to clinical testing.
• Bioanalytical immunoassay knowledge and application of analytical platforms to regulated analysis.
• Detail-oriented with excellent organizational skills.
• Willingness to travel.
  

What We Offer You:

We put our employees at the center of everything we do and are committed to providing them, and their families, with benefits that meet their diverse and changing needs. We invest in integrated benefits programs and resources to take care of our employees’ physical, mental and emotional, financial, and social well-being so they can thrive at home and at work, at any stage of their well-being journey.

To learn more about our benefits, visit https://jobs.iqvia.com/benefits.

If you’re looking to unleash your potential, join IQVIA Laboratories to help make the extraordinary possible!

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

The potential base pay range for this role, when annualized, is $113,900.00 - $189,800.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What We Are Looking For:

• B.S. diploma is a minimal requirement.
• A minimum of 10 years of experience in the pharmaceutical or clinical trial environment, including experience with immunoassay.
• M.S. and/or Ph.D. diploma is preferred.
• Other equivalent combinations of education, training, and experience may be accepted in lieu of a degree.
  
  

The Knowledge, Skills, and Abilities needed for this role:

• Strong knowledge/experience with LCMS.
• General knowledge of GXP laboratory regulations.
• Sound scientific and technical knowledge as it relates to clinical testing.
• Bioanalytical immunoassay knowledge and application of analytical platforms to regulated analysis.
• Detail-oriented with excellent organizational skills.
• Willingness to travel.