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@cancergenetics.com
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Glenn Smits is listed as World-wide and World-class Preclinical Research for the Med Tech Industry at NAMSA, based in New Richmond, Wisconsin, United States. AeroLeads shows a work email signal at cancergenetics.com and a matched LinkedIn profile for Glenn Smits.
Glenn Smits previously worked as Vice President of Global Preclinical Research at Namsa and Founder at "3S Llc" (Smits Scientific Solutions Llc). Glenn Smits holds Phd, Pharmacology from Saint Louis University.
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AeroLeads found 1 current-domain work email signal for Glenn Smits. Compare company email patterns before reaching out.
I am a team-oriented leader, with solid scientific credentials and experience, covering a wide range of therapeutic areas and treatment modalities. I have established research, program, and business plans and budgets; built and managed effective networks of KOLs and clients; managed in matrix-aligned organizations, and advanced programs leveraging both authority and influence. My career has spanned large pharmaceutical companies, biotech companies, and contract research organizations, with positions ranging from scientific to senior management. My scientific focus has been primarily in cardio/renal/metabolic disease areas with additional extensive experience in oncology, immuno-oncology, fibrosis, immunological disorders, and neurological diseases. I have extensive experience in GLP-compliant safety assessment across geographies. I have extensive network of connections within the CRO industry, especially pre/non-clinical focused CROs.
Listed skills include Drug Discovery, Pharmacology, Clinical Development, Biotechnology, and 46 others.
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Toledo, Oh, Us
Provides leadership and strategic direction for the Global Preclinical Interventional and Surgical Research (ISR) program for NAMSA, at our sites in Minneapolis MN, Northwood OH, Diest Belgium, and Lyon France.
Cherry Hill, Nj, Us
San Francisco, California, Us
As Scientific Writer, I provide writing services to Clinovo's clients, including clinical evaluation plans and reports for regulatory submission, scientific/clinical manuscripts for submission to peer-reviewed journals, preparation of presentations (powerpoint slide-decks, posters, etc.), and others.
Mattawan, Mi, Us
The Vice President of the Discovery Center is responsible for the strategic direction, growth, and performance of the Discovery Center of MPI Research, which includes the following Product Lines: ADME (Absorption, Distribution, Metabolism, and Excretion), Pharmacokinetics (PK), Surgery and Experimental Therapeutics (ET). The Senior Directors/Directors of ADME, PK, Surgery, and Experimental Therapeutics (as well as other Departments, such as Molecular Imaging, Cell & Molecular Biology, and Product Lines that may comprise the Discovery Center) report to the Vice President of the Discovery Center.
Provide consulting services to biotech, pharma, and medical device companies.
Wilmington, Massachusetts, Us
Direct and oversee the execution and quality of scientific research within the site. Assure all scientific processes and practices meet or exceed client needs. Direct the development, interpretation, implementation and achievement of short- and long-range scientific objectives for the site. Ensure program integration and optimization of group function and business unit. Recommend and implement techniques and practices to improve productivity, increase efficiencies, cut costs, take advantage of opportunities, and maintain state-of-the-art practices.
Establish and build a pharmacology and pharmacokinetics team to support internal drug discovery projects. Coordinate and manage external contract research studies and supervise internal laboratory and staff. Internal capabilities include bioanalytical capabilities (LC/MS/MS, ELSD, UV) and in vitro drug metabolism and toxicity.
Cambridge, Ma, Us
Pharmacology for adenosine project(s). Serve on Adentri Program Team, Adentri Strategy Team, Adentri Clinical Development Plan committee, and direct the Adentri Research Team. Recruited and built capabilities; from cloning and expression, radioligand binding, in vitro assays, in vivo pharmacokinetics/pharmacodynamics and safety assays and in vivo efficacy models. Plan, write and review regulatory submissions (Pre-IND, IND, NDA). Establish rodent models of fibrosis, congestive heart failure, renal function, hemodynamic profiling, isolated heart and vessels, thrombosis and other models in-house and manage collaborations with external investigators. Provide general pharmacology support to other programs at Biogen. Initiate novel drug discovery programs. Serve on Scientific Review Committee and Scientist Promotion Committee. Directed efforts of Molecular Pharmacology group, PK/PD group and Fibrosis Pharmacology group (each group consisting of PhD Scientist and 2 to 4 associates).
Browns Mills, New Jersey, Us
Independent research pertaining to physiology and patho-physiology of myocardial ischemia/reperfusion injury and vascular proliferation (restenosis). Areas of particular interest are: role of immediate-early gene (EGR-1) expression in vascular proliferation and the regulation of transcription of these genes; effects of adenosine receptor activation on ischemia/reperfusion injury; role of leukocytes and free radical generation in reperfusion injury and stimulation of cardiomyocyte apoptosis; cardio- and vasculo-protective effects of heat shock protein induction; mechanisms of ischemic preconditioning; mechanisms of myocardial stunning.
In vivo pharmacology, primarily ischemia/reperfusion injury and hemodynamics. Developed concept of utility of a mixed A1/A2a Adenosine agonist as treatment of reperfusion injury; designed, conducted, and managed non-clinical studies in acute ischemia/reperfusion injury models; assembled justification for clinical development of the mixed A1/A2a adenosine agonist AMP579; contributed non-clinical pharmacology section of AMP579 IND. Establish rat and pig models of myocardial ischemia/reperfusion injury and rat model of acute renal failure. Perform balloon injury model in porcine coronary arteries. Instrumentation of rat and dog for telemetry measurement of arterial pressure and locomotor activity. Wrote sections of IND applications. Supervise research associates.
Us
In vivo pharmacology of vasoactive agents and antagonists. In vivo experimentation to support ongoing research projects of Cardiovascular Disease team. Develop models of hypertension in rat, dog and pig. Investigation of roles of angiotensin, bradykinin and atrial natriuretic peptide in hypertension, heart failure and myocardial ischemia and effects on renal function. Managed in vivo team for Angiotensin II antagonist project. Initiated project for imidazoline receptor agonists. Several projects resulted in clinical evaluation (atrial natriuretic peptides and Angiotensin II receptor antagonist). Contributed to IND reports. Supervise research associate.
Quick answers generated from the profile data available on this page.
Glenn Smits works for NAMSA.
Glenn Smits is listed as World-wide and World-class Preclinical Research for the Med Tech Industry at NAMSA.
AeroLeads has found 1 work email signal at @cancergenetics.com for Glenn Smits at NAMSA.
Glenn Smits is based in New Richmond, Wisconsin, United States while working with NAMSA.
Glenn Smits has worked for Namsa, "3S Llc" (Smits Scientific Solutions Llc), Orange Grove Bio, Vyant Bio, and Vivopharm Llc.
You can use AeroLeads to view verified contact signals for Glenn Smits at NAMSA, including work email, phone, and LinkedIn data when available.
Glenn Smits holds Phd, Pharmacology from Saint Louis University.
Glenn Smits is listed with skills including Drug Discovery, Pharmacology, Clinical Development, Biotechnology, Cro, In Vivo, Glp, and Drug Development.
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