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Scientific Affairs Specialist

Company: ChromaDex
Location: Longmont
Posted on: June 15, 2019

Job Description:

ChromaDex Corp. is an integrated, global nutraceutical company devoted to improving the way people age. ChromaDex's scientists partner with leading universities and research institutions worldwide to uncover the full potential of NAD and identify and develop unique, science-based ingredients. Its flagship ingredient, NIAGEN-- (nicotinamide riboside), sold directly to consumers as TRU NIAGEN--, is backed with clinical and scientific research, as well as extensive IP protection. TRU NIAGEN-- is helping the world AGE BETTER--. The Scientific Affairs Specialist will work under the guidance of the Director of Technology to facilitate the material transfer agreement (MTA) program, create scientific and technical content to support ChromaDex's Scientific Affairs Team and research programs. The range of content includes but is not limited to: providing day-to-day support for the management of the material transfer agreement (MTA) program including maintaining technical documents, conducting literature reviews with annotated bibliographies and developing internal scientific reports in addition to assisting in protocol development. -- The Scientific Affairs Specialist will frequently interact with researchers from outside organizations and provide technical support in protocol development, modification and implication. Additionally, the specialist will frequently search, read, synthesize, and summarize literature from a broad range of research areas to support ongoing research development and communications efforts. -- Main duties include: Facilitate and interact with independent researchers interested in conducting research with ChromaDex through our Material Transfer Agreement (MTA program). Create original[RL1] [JR2] [AE3] scientific documents that are accurate, credible, and appropriate for a scientific audience. Spearhead exploration of the scientific literature to support new areas of interest. Review, summarize, and prioritize MTA requests with outside research parties. Maintain up-to-date published research relating to NAD, NR and other innovative interventions. Involvement in preclinical protocol/technique development in addition to preclinical study design and implementation. Assist in clinical study design, implementation and manage clinical product needs. Required Competencies: Excellent technical writing ability - written content primarily for scientific audiences and research organizations. Demonstrated ability to read, accurately distill, and appropriately synthesize research and interpretation of data representing a variety of biology subdisciplines. Solid understanding of biochemistry and molecular biology as well as their application to human health and physiology. Solid understanding of in-vitro and ex-vivo laboratory analysis techniques. -- Desired Skills/Knowledge: Strong verbal communication skills and aptitude for working on teams in a high energy and dynamic work environment. Expertise in research areas related to inflammation, metabolic stress, aging or mitochondrial health. Expertise in method and protocol development. Strong organization and prioritization skills. Potential to learn how to translate science to non-technical audiences. Ability to shift priorities quickly depending on company focus. -- Training, Education and Experience: Master's degree in biochemistry, cellular and molecular physiology or related field. 2+ years of industry or academic experience. Proven technical writing skills and experience writing methodology and literature reviews. -- Working Conditions: Must be able to perform routine tasks repeatedly, efficiently, and accurately in a timely manner, occasionally lifting up to 30 lbs. Must be capable of understanding, listening and following verbal and written instructions to accomplish desired goals and have the ability to communicate verbally and in writing at all levels of the organization. Fast paced and dynamic office/laboratory environment. --Potential exposure to carcinogens, corrosives and other chemicals. Travel domestically and internationally up to 5% of the time. -- ChromaDex offers benefits to eligible employees who have met all requirements for enrollment. Benefits include medical, dental, vision, matching 401(k) and more. ChromaDex maintains a website at to which ChromaDex regularly posts copies of its press releases as well as additional and financial information about the Company. ChromaDex (and its affiliates) is an equal employment opportunity employer and does not discriminate on the basis of race, sex, national origin, religion, physical handicap, marital status, veteran status, sexual orientation or any other basis prohibited by law.

Keywords: ChromaDex, Denver , Scientific Affairs Specialist, Other , Longmont, Colorado

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