A large and global pharmaceutical company is seeking candidates for a leadership job in applied toxicology. The person hired for this role will lead and expand the company’s reach in respect to product risk characterization, assessment of contaminants, leachables and impurities and develop standards for occupational and environmental exposures. He/She will regularly interact with regulatory authorities globally and assure that the company is compliant in respect to relevant regulations. The person hired for this role will initially supervise one fellow toxicologist.
Requirements include a graduate degree in Toxicology or a related public health science and ten or more years of experience in pharmaceutical occupational/environmental toxicology and related manufacturing safety standards. An ability to collaborate with colleagues in many disciplines is essential to this person’s success.
Reporting to the Senior Director of Drug Safety, the position will work from an office near Boston, with some flexibility for an alternate location, as needed.
Search Assignment #1358
Our client company is a rapidly growing and privately owned consumer goods company with interests in personal care, home care and the nutritional/supplement markets. The company has recently hired a VP for regulatory and product safety matters. One of her first priorities in building a group is to hire an experienced toxicologist/product safety professional.
The VP would like to hire a person with a PhD in Toxicology, or a related science, and at least a few years of experience in product safety and/or ingredient risk assessment. Experience in the consumer goods, chemical, food or related industries is desired.
The initial responsibilities will include safety assessment of finished products and ingredients, to include preparation of the necessary dossiers for global regulatory authorities, internal and external collaboration on product safety matters and assuring compliance with global inventory regulations (REACH, TSCA etc.).
Since the function is new within the company, the VP to whom this job reports will seek a person with good organizational skills to help envision the future of the department, to include an expanded product safety function.
Uniquely, the company is located in the Rocky Mountain states, adjacent to some of the West’s outdoor recreational assets, with a slower pace of life than the places where many consumer companies are located. At this time the hiring manager is seeking a person willing to relocate, with some possibility the position will be filled remotely, with periodic travel to headquarters.
Search assignment #1351
One of the world’s most respected pharmaceutical companies has engaged The Leyden Group to assist in the search for a senior environmental toxicologist. The person hired for this role will be considered up to an Associate Director title and will report to a Director, within the company’s Environmental and Stewardship Department.
A PhD in Toxicology or a related subject matter is required, as is at least five years of applied experience in toxicology, environmental fate/effects and/or risk assessment. Prior experience in the pharmaceutical industry is not required.
The initial focus of the job will be in the planning and oversight of toxicology and fate/effects testing, with follow up analysis associated with global regulatory requirements for drug approvals. This person will also have manufacturing site responsibilities pertaining to environmental toxicology and risk assessment and will participate on working groups with global trade associations.
In the future, the person hired for this role will participate in company and industry wide sustainability and environmental stewardship initiatives. The position could be located at one of several company sites in the Eastern U.S., the U.K., Australia or Switzerland. A fully remote working arrangement is not being offered.
Search assignment #1371
A large and global pharmaceutical company based in California has engaged The Leyden Group to identify an early career toxicologist. The person hired for this role will work in the company’s development phase, regulatory toxicology group, reporting to an Associate Director of Toxicology.
Typical responsibilities will include serving on drug development project teams, acting as a Study Monitor on externally conducted research, preparing summaries and dossiers for FDA and other regulatory approvals and acting as a toxicology subject matter expert within their area of training.
The company is seeking a PhD in Toxicology or a related discipline. Experience could include postdoctoral or traditional tenure (less than five years) in a pharmaceutical company, or a few years of experience in a contract research laboratory where GLP studies are conducted. Previous experience could be in discovery or development phase toxicology. In addition to the technical skillset, the person must be highly collaborative and have strong interpersonal skills.
Search assignment #1347
A highly successful, mid-sized, pharmaceutical company has engaged The Leyden Group to identify an experienced, ACVP Boarded Pathologist with broad drug safety/drug development skills. At least five years of such experience is needed. The company’s pipeline includes small molecules, biologics and gene therapy based compounds, thus broad exposure to various pharmaceutical modalities is desired.
The person hired for this role will act as the sole Pathologist in an existing Toxicology/Pharmacology Department. He/She will have responsibilities ranging from typical anatomic and clinical evaluation of tissues on GLP and non-GLP studies, peer review of collaborations/externally conducted studies through making important contributions to drug safety strategy from the pathology perspective. The person hired for this role will participate as an active member of Pre-Clinical discovery and development project teams.
The position, reporting to the company’s Head of Pharmaceutical Sciences (within a Translational Medicine Department), can work remotely, or from the company’s research headquarters in Northern California.
Search assignment #1360
The Leyden Group is partnering with a large, San Diego based drug company seeking to expand their discovery/investigative phase toxicology program. The position will report to the Director of Discovery Toxicology at the site.
A graduate degree and two or more years of pharmaceutical discovery toxicology (or closely related) experience is desired. A more experienced person (5+ years) could be hired at a higher grade level as well.
This non-laboratory position will act as a project team representative/advisor for the selection and interpretation of early phase in-silico, in-vitro and in-vivo studies for early drug candidate risk assessment. The company works across many disease targets and modalities.
The company offers career growth opportunities in both discovery and/or regulatory toxicology realms and provides a strong compensation, benefit and equity compensation.
Search assignment #1363
Our client (based in Connecticut) is a small and emerging company which is developing specialty chemicals for agricultural uses. The leadership team and Science Advisory Board is composed of several people with a long track record in the industry.
As part of their growth, the company seeks its first toxicologist, the person who will manage safety assessment of R&D compounds in the company’s discovery and development pipeline. The person will report to the company’s VP of Operations.
They seek a PhD toxicologist with three or more years of relevant experience. While agrochemical experience is desired, scientists with other experiences will be considered. Specific experience in safety assessment study design and CRO monitoring is important.
Knowledge in the use of in-silico and computational tools for predictive safety screening is desired. Experience with regulatory requirements for human and environmental toxicology is preferred.
The person hired for this role will manage toxicology testing and assessment programs and collaborate with his/her colleagues in the product development and regulatory approval process. The person will also develop the use of various QSAR and in-silico tools as part of the safety assessment effort.
Search assignment #1258