Scientist, Scientific Affairs

Unicity International, Inc.; Las Vegas (NV); Hybrid; USD 110,000 - 170,000; Full time

Benefits offered by this job

Health, dental, vision, life benefits

Paid parental leave

Generous vacation & company holidays

401(k) with company match

Job summary

Unicity USA Inc. is seeking a Scientist, Scientific Affairs to serve as a resident expert on health and nutrition, guiding claims validation, bioactive ingredients assessment, and research program coordination for internal and external partners.

You will design fit-for-purpose studies, lead internal and external studies, translate science into marketing content, and collaborate with R&D, Regulatory, and Legal to ensure FDA/FTC compliance. Remote possibilities and travel up to 20% are noted.

Qualifications

• MS/PhD in nutrition, biochemistry, chemistry, or related field
• 3+ years (MS) or 1+ years (PhD) of clinical research experience
• Ability to review scientific literature and apply findings to product development
• Extensive knowledge of nutraceutical industry trends and health claims
• Understanding of GCP, ICH E6, HIPAA; knowledge of DSHEA and FTC/FDA standards
• Experience designing and overseeing protocols, IRB submissions, and studies (preferred)

Responsibilities

• Serve as scientific subject matter expert for internal teams on ingredients, claims, and product positioning
• Coordinate internal/external clinical studies and real-world evidence
• Translate science into compliant content for marketing, training, and sales
• Prepare reports, white papers, and publications accurately representing study results
• Develop substantiation procedures with R&D, Regulatory, and Legal
• Review marketing content for technical accuracy and regulatory compliance

Skills

Strong communication skills

Interpersonal skills

Analytical abilities

Organizational skills

Education

MS/PhD in nutrition/biochemistry/chemistry/biology

Job description

Career Opportunities with Unicity USA Inc

A great place to work.

Careers At Unicity USA Inc

Current job opportunities are posted here as they become available.

Scientist, Scientific Affairs - Provo, UT

Unicity is dedicated to developing innovative, science-based products and programs that promote metabolic health and improve the quality of life for people everywhere. For over 30 years, Unicity has been dedicated to developing high-quality products that contain the vital nutrients your body needs. With the proper process, cutting-edge technology, and a mission to Make Life Better, Unicity is paving the way for a better tomorrow.

In addition to competitive pay, we offer:

• Health, dental, vision, life and other benefits that begin within a month
• Paid parental leave
• Generous vacation allowance in addition to company-paid holidays
• 401(k) with company match

Responsibility:

The Scientist, Scientific Affairs, will be a resident expert on health and nutrition matters including providing guidance on the technical validity of claims, technical assessment of bioactive ingredients, and coordination of research programs internally and with external partners, including design and execution of fit-for-purpose clinical studies.

You're Right For This Job If You Can:

• Serve as the scientific subject matter expert for internal teams on functional benefits, ingredients, formulations, and product positioning, including risk assessments.
• Assess the current portfolio and recommend improvements in ingredients and functional benefits, and develop new product and ingredient claims and health and nutrition propositions.
• Track emerging health trends and new research, and share insights and future opportunities with leadership.
• Validate the safety, efficacy, and regulatory status (e.g., GRAS, NDI) of botanical and bioactive ingredients.
• Design fit-for-purpose studies: match the research question, endpoints, population, and study size to the claim, the timeline, and the budget.
• Independently lead internal studies, real-world evidence and consumer studies, and decentralized clinical research. This includes writing protocols, informed consent forms, and IRB submissions, and overseeing study conduct, data quality, and analysis.
• Coordinate external scientific and clinical testing, and build relationships with key opinion leaders and clinical research organizations.
• Develop and substantiate claims to FTC and FDA standards, support claims review for international markets (e.g., EFSA, Health Canada), and build substantiation procedures and documents with R&D, Regulatory, and Legal.
• Translate science into accurate, compliant content and training for marketing, sales, and distributors. Review and approve marketing content and advertising for technical accuracy, and present at company events.
• Prepare reports, white papers, and publications that accurately represent internal and clinical study results.

You'll Thrive in This Role If You Can:

• Design fit-for-purpose studies that are scientifically valid and support target claims within feasibility, timeline, and budget constraints
• Make informed decisions with limited or emerging evidence and iterate quickly
• Work independently and take ownership of projects from start to finish
• Partner with marketing, R&D, and the executive team, including recommending defensible alternatives when a claim is not supported
• Think creatively to differentiate products in a crowded market

Qualifications

• Master’s of Science (M.S.) or Doctor of Philosophy (Ph.D.) degree or higher in a technical field (nutrition, biochemistry, chemistry, exercise and sports science, food science, biology, etc.)
• Masters with 3+ years, or Ph.D. with 1+ years of clinical research experience
• Ability to search, understand, and apply the scientific literature in developing science-based products to maintain and improve human health
• Extensive knowledge of human health and current trends in the nutraceutical industry
• Good interpersonal, analytical, and organizational skills
• Must have strong oral and written communication skills including the ability to explain science to non-scientific audiences
• Understand GCP, ICH E6, and HIPAA requirements
• Working knowledge of dietary supplement regulations (DSHEA) and FTC and FDA standards for claims substantiation
• Ability to develop study protocols and procedures required in all aspects of conducting scientifically valid internal and external studies
• Working knowledge of statistics
• Preferred: experience in dietary supplements, functional foods, pharma, or a CRO; IRB submissions; peerreviewed publications

Location and travel: Our ideal candidate can travel and work in-office as needed to conduct internal studies at our Provo, Utah, or Las Vegas, Nevada offices. We are open to remote work for the right candidate. Travel: up to 20% for study sites, conferences, and company events.