Senior Medical & Scientific Advisor - LCMS

Weingart Foundation; Deutschland; Remote; USD 113.000 - 190.000; Vollzeit

Zusammenfassung

A leading healthcare organization is looking for a Senior Medical and Scientific Advisor (LC-MS) to provide scientific and technical guidance for drug development. The ideal candidate has over 10 years of experience in the pharmaceutical sector and strong knowledge of LC-MS. This remote role involves ensuring compliance in bioanalytical strategies and collaborating with various stakeholders globally. Competitive salary range of $113,900 - $189,800 is offered.

Leistungen

Integrated benefits programs

Commitment to employee well-being

Qualifikationen

• Minimum 10 years of experience in the pharmaceutical or clinical trial environment.
• Experience with regulated bioanalysis and ICH M10 required.
• Other equivalent combinations of education, training, and experience may be accepted.

Aufgaben

• Provide scientific and technical advice for bioanalytical strategy.
• Lead scientific escalations and participate in laboratory investigations.
• Support scientific discussions to ensure regulatory compliance.

Kenntnisse

Strong knowledge/experience with LC-MS

General knowledge of GxP laboratory regulations

Detail-oriented and goal-oriented

Excellent organizational skills

Ability to work across interdisciplinary teams

Ausbildung

B.S. diploma

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

Jobbeschreibung

We are seeking a Senior Medical and Scientific Advisor (LC-MS) 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 (LC-MS), 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:

• Ensure Early Engagement between bioanalytical scientists to provide input on regulated LC-MS assays and platforms
• Support scientific discussions concerning assays to ensure fit with study/customer needs and regulatory compliance
• Drive evaluation of new LC-MS technology
• Participate in laboratory investigations and lead scientific escalations
• Work with Marketing and Commercial to create scientific client-facing material
• Nurture innovation through knowledge of emerging technologies
• Contribute to scientific governance meetings
• Utilize extended capabilities of parent organization in leveraging expertise
• Provide scientific/tech support for bid defense prep and capability presentations
  

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 regulated bioanalysis and ICH M10.
• 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 LC-MS.
• General knowledge of GxP laboratory regulations and operations.
• Sound scientific and technical knowledge as it relates to quantitative LC-MS in support of pharmacokinetic and pharmacodynamic studies.
• Ability to apply scientific knowledge to marketing and commercial objectives.
• Detail-oriented, goal oriented, with excellent organizational skills.
• Demonstrated ability to work across interdisciplinary teams.
• Willingness to travel and present to bioanalytical audiences.
  

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 regulated bioanalysis and ICH M10.
• 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 LC-MS.
• General knowledge of GxP laboratory regulations and operations.
• Sound scientific and technical knowledge as it relates to quantitative LC-MS in support of pharmacokinetic and pharmacodynamic studies.
• Ability to apply scientific knowledge to marketing and commercial objectives.
• Detail-oriented, goal oriented, with excellent organizational skills.
• Demonstrated ability to work across interdisciplinary teams.
• Willingness to travel and present to bioanalytical audiences.