QUALIFICATIONS: Over twenty years
drug development experience ranging from pre-clinical pharmacology / toxicology to managing and directing clinical and cross functional teams in the conduct and execution of global, clinical trials.
Our approach is shaped by an experienced team with deep
drug development experience, and productive collaborations with world - class advisors and partners.
Not exact matches
Jennifer has more than 20 years of regulatory
experience, integrating regulatory strategy into
drug development and precision medicine across multiple therapeutic areas.
In January 2017, SiteOne announced the closing of a research and
development agreement with Amgen, a collaboration focused on combining SiteOne's
experienced drug discovery team and portfolio of novel Naᵥ1.7 inhibitors with Amgen's neuroscience capabilities.
«Her breadth of
experience in biomedical research and
development can benefit Exelixis greatly as the company recommits its resources to
drug discovery and bolstering its pipeline following the successful ongoing commercialization of its lead medicine, CABOMETYX.»
The Company uses its
experience to guide progress into clinical trials, ultimately leading to successful
drug development and value realisation for its investors.
The Minoryx team is made up of a group of
drug discovery and
development experts with several decades of
experience in biotech and pharma.
Experience in orphan disease
drug development and an understanding of genetic concepts and molecular biology laboratory techniques is beneficial.
Douglas Loe, healthcare equity analyst with Echelon Wealth Partners, brings more than a decade of
experience to financial analysis in the global
drug development, medical technology, healthcare services and specialty pharmaceutical sectors.
It tells the story of «the guinea pigs»» the people most likely to be research subjects in Phase I trials, which test the safety of a
drug under
development by giving it to healthy subjects and examining any side effects they
experience.
Taking antibiotics when they are not needed creates additional health risks as it increases the chance a patient will
experience an adverse
drug reaction, and also leads to the
development of antibiotic - resistant bacteria which affects everyone in the community.
This juncture between basic research and the
drug development process first began to interest Conley when she was still a postdoc at Michigan, where she had an «amazing
experience» in a «world - renowned research lab.»
Development of the
drug was stopped after some patients
experienced a reduction in cholesterol lowering over time.
It hits many desirable highlights: postdoc
experiences as a Fullbright scholar and a visiting scientist at the National Cancer Institute (NCI), many dozens of published papers and patents, and a long list of impressive job titles from
drug companies to law and venture capital firms to state economic
development organizations.
Given its prolonged
development into adulthood, this region is particularly susceptible to being shaped by life
experiences in adolescence, such as stress and
drugs of abuse.
Understanding the entire
drug development process, however, necessitates
experience in big pharma.
We had been looking for a senior scientist with
experience in high throughput screening (HTS) assay
development for a large
drug discovery research program.
With our extensive pharmaceutical / biotech
drug discovery and
development experience, we are well - positioned to drive projects toward an end goal that will ultimately benefit patients.
Dr. Kanner brings more than 25 years of
experience in
drug discovery and
development and will lead Caribou's research and
development of new applications for its gene editing technology.
The SGC is a global network of
experienced academic and industry scientists that will contribute expertise in the
development of reagents required for target validation and
drug discovery.
12 years of expertise in metabolomics for
drug discovery in the pharmaceutical industry and in the
development of innovative analytical methods for biomarker analysis, with
experience in metabolomics and imaging technologies coupling.
She is CEO of PsychoGenics Inc., a profitable preclinical CNS service company, CEO of PGI
Drug Discovery LLC, a company engaged in psychiatric drug discovery with three partnered Phase II clinical programs and Adjunct Associate Professor of Neuroscience at Mount Sinai School of Medicine, Dr. Leahy has more than 25 years of experience in drug discovery, clinical develop and business development for pharmaceutical and biotechnology companies, including extensive knowledge of technology assessment, licensing, mergers and acquisitions, and strategic plann
Drug Discovery LLC, a company engaged in psychiatric
drug discovery with three partnered Phase II clinical programs and Adjunct Associate Professor of Neuroscience at Mount Sinai School of Medicine, Dr. Leahy has more than 25 years of experience in drug discovery, clinical develop and business development for pharmaceutical and biotechnology companies, including extensive knowledge of technology assessment, licensing, mergers and acquisitions, and strategic plann
drug discovery with three partnered Phase II clinical programs and Adjunct Associate Professor of Neuroscience at Mount Sinai School of Medicine, Dr. Leahy has more than 25 years of
experience in
drug discovery, clinical develop and business development for pharmaceutical and biotechnology companies, including extensive knowledge of technology assessment, licensing, mergers and acquisitions, and strategic plann
drug discovery, clinical develop and business
development for pharmaceutical and biotechnology companies, including extensive knowledge of technology assessment, licensing, mergers and acquisitions, and strategic planning.
Dr. Joyal has over 20 years of
drug discovery
experience with expertise in cell and molecular biology, particularly in the areas of receptor biology, cell signaling pathways, and assay
development.
Having a strong R&D department with great
experience and expertise in
drug development, animal model and assay
development and preclinical efficacy evaluation, the contribution of Biomedcode has been greatly valued by our partners, as documented by our participation in several collaborative research projects.
Experience with DMPK and early
drug development in metabolic disease, inflammation and oncology
Jörg brings over 17 years»
experience in
drug discovery and
development across key areas such as oncology, infectious diseases, vaccinology, and autoimmunity, with a focus on peptide and nucleic acid - based therapeutics.
Candidates should have a passion for
drug development with extensive
experience in IND - filing and early clinical
development.
Erik is a biopharmaceutical
development and operational professional with more than 20 years of
drug development, project management and manufacturing / operational
experience in pharmaceutical and biotechnology companies in North America and Europe.
At QPS, translational medicine brings together leading - edge technologies and pharmaceutical R&D
experience to create a business service unit that works efficiently to advance your
drug development program.
The new advisors, some of the most wellrespected individuals in their fields, were specifically sought for the wealth of
experience they bring to bear on Foundation efforts to advance
drug development in SMA: Paul S. Anderson, PhD, retired vice president for Chemistry at Merck, G. Stephen DeCherney, MD, MPH, president of Clinical Development Services Americas for Quintiles Transnational Corp., Corey S. Goodman, PhD, president and chief executive officer of Renovis, Inc., Jonathan S. Leff, managing director at Warburg Pincus LLC and responsible for the firm's life sciences investment effort, John H. Park, Partner at Blum Capital Partners, LP, and Wesley Thompson, PhD, professor of Neurobiology at The University of Texas
development in SMA: Paul S. Anderson, PhD, retired vice president for Chemistry at Merck, G. Stephen DeCherney, MD, MPH, president of Clinical
Development Services Americas for Quintiles Transnational Corp., Corey S. Goodman, PhD, president and chief executive officer of Renovis, Inc., Jonathan S. Leff, managing director at Warburg Pincus LLC and responsible for the firm's life sciences investment effort, John H. Park, Partner at Blum Capital Partners, LP, and Wesley Thompson, PhD, professor of Neurobiology at The University of Texas
Development Services Americas for Quintiles Transnational Corp., Corey S. Goodman, PhD, president and chief executive officer of Renovis, Inc., Jonathan S. Leff, managing director at Warburg Pincus LLC and responsible for the firm's life sciences investment effort, John H. Park, Partner at Blum Capital Partners, LP, and Wesley Thompson, PhD, professor of Neurobiology at The University of Texas at Austin.
The trial is being managed by the charity's highly
experienced Drug Development Office.
SAN DIEGO, March 28, 2017 (GLOBE NEWSWIRE)-- Invivoscribe ® Technologies Inc., a global company with decades of
experience providing internationally standardized clonality and biomarker testing solutions for the fields of oncology, personalized molecular diagnostics ®, and personalized molecular medicine ®, reports that its next - generation sequencing (NGS) LymphoTrack ® Assay kits are being used by its LabPMM ® clinical laboratories, pharmaceutical partners, and cancer centers to identify and monitor chimeric antigen receptor T - cells (CAR - T) and engineered T - cell receptors in peripheral blood of subjects in support of immuno - therapeutic
drug development and treatment regimen
development for both hematologic and solid tumors.
She has
experience in small molecule and large molecule
development for both oncology and non-oncology indications and has a strong interest in developing alternative in vitro and in vivo methods to assess safety and efficacy outside of the traditional
drug development paradigm.
Dr. Lui has seven years of
experience working in preclinical
drug development and target validation in academia and industry.
So, whereas the typical person might think of their «environment» as their house, or their neighborhood - scientists trying to understand the factors that influence the
development of schizophrenia define environment to include everything from the social, nutritional, hormonal and chemical environment in the womb of the mother during pregnancy, up to the social dynamics and stress a person
experiences, to street
drug use, education, virus exposure, vitamin use, and much, much more.
For example, the superbug MRSA, which can cause hard - to - treat skin infections, appears to contaminate approximately 5 % of U.S. retail meat; mysterious skin hives or allergic reactions may be a sign of alpha - gal meat allergies; a lack of safety thresholds in U.S. meat for
drug residues, toxic metals, and pesticides can potentially result in jaundice and skin cancer; a case of Vitamin A poisoning from fish actually resulted in one man
experiencing such serious peeling of his skin it took more than three months to heal; using tanning beds instead of natural sunlight or supplements to get Vitamin D is linked to an increased risk of the deadliest kind of skin cancer; milk consumption has been associated with increased acne risk; and low antioxidants levels in the skin may correlate with the
development of wrinkles.
The veterinary leadership
experience and the AVMA leadership convention were great
experiences as well; they really helped with my leadership
development, really helped with my networking, and meeting veterinarians all ready out in the profession and in the various industries, like in the
drug companies and along those lines.
By maintaining a commitment to continuous improvement, promoting the professional
development of our employees, and continuing our dedication to quality and customer service, Diamondback
Drugs will offer a «best in class» customer
experience.
She has more than 30 years of
experience working with pharmaceutical companies and the FDA in product discovery, protocol review and new
drug development.
It's almost like their
development teams build the characters, stories, and battle system and then smoke a bunch of crack and decide in a
drugged up haze on a range of other features that will «enhance» the
experience.
An
experienced drug injury lawyer needs to stay on top of investigative
developments and new information that comes to light.
Key
developments in the case law reflect trends that employers are
experiencing: sexual harassment,
drug testing and addressing mental health in the workplace.
Her
experience in Government includes initiatives such as the
development of the Provincial Immigration strategy, the establishment of the Global Food Institute, the Sylvia Fedoruk Canadian Centre for Nuclear Innovation, establishment of Innovation Saskatchewan, construction of the first Women's Shelter built by the Provincial Government since 1989, the creation of the Office of the Counsel for Children, and changes to the Human Rights Code regarding transgender persons and Kate's Place, a supportive residence for women who are attending Regina
Drug Treatment Court.
Our team of
experienced trial and appellate lawyers craft and execute comprehensive intellectual property strategies from initial
drug development through trial and appeal.
Summary:
Experienced cell / molecular biologist with background in bioanalytics, cell - based & ligand bind - ing assay
development / validation, early discovery of therapeutic biologics and anticancer
drugs.
Chemical engineer professional with
experience in research and
drug development, member of the scientific community, looking for a job as chemical engineer in a prestigious pharmaceutical company that can offer me the opportunity to develop professionally.
• Highly
experienced in the assessment of patient care needs and
development of nursing care plans, particularly providing acute care for a diverse population including patients
experiencing drug and alcohol withdrawal, wound care, oncology and dialysis • Proficient in handling details of medical administration and providing assistance in emergency cases.
Bringing 6 years» hands - on
experience in developing and implementing core programs to meet the needs of young people, pertaining to education, self -
development, homelessness, family ties, and
drug and alcohol abuse.
She is responsible for sales, business
development, marketing, and client success and has 25 years of
experience in background screening,
drug testing, and occupational health testing.
Worldwide About Blog Camargo Pharmaceutical Services is the most
experienced global strategist providing comprehensive
drug development services specialized for the 505 (b)(2) approval pathway and global equivalent processes.