Andrea Wolff Email and Phone Number
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Andrea Wolff personal email
With a strong foundation in drug transport and metabolism research, my tenure at XenoTech has honed my skills in contract research. My role as Director of Laboratory Logistics encompasses a broad spectrum of responsibilities, including fostering employee growth through coaching, the successful implementation of innovative processes, and ensuring compliance with stringent industry practices all to ensure our client's needs are meet and safe drugs are developed. Leveraging my expertise in contract service work and leadership, I am able to work collaboratively across departments to cultivate improvements and advancements for our company. This includes developing, implementing, and adopting an electronic lab notebook to streamline our processes while maintaining the high standards required of a GLP facility.
Xenotech
View- Website:
- xenotech.com
- Employees:
- 119
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DirectorXenotech Jun 2017 - PresentKansas City, Kansas, United StatesDirects the management of several departments and project management functions. Assumes the responsibility for daily operations and the quality and timelines associated with contract research deliverables. Business responsibilities include encouraging and leading innovation, problem solving, empowering employees, managing change, effectively communicating, and planning and driving company initiatives to achieve the intended goal.
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Principal Scientist - Program OversightSekisui Xenotech, Llc Apr 2016 - Jun 2017Head of program oversight department. Serves as management on multiple nonclinical, drug metabolism and transport-related contract studies. Job responsibilities include but are not limited to preparing research protocols and cost estimates; designing studies based on regulatory guidelines and client needs; managing study schedules; supervising multiple study directors; coordinating the day-to-day activities of the department; managing new scientific projects and R&D efforts for the department; ensuring the department adheres to Good Laboratory Practice regulations and company policies and procedures; writing and maintaining Standard Operating Procedures (SOPs); preparing and administering departmental budgets; critically reviewing data from both a scientific and regulatory perspective; troubleshooting technical problems; training study directors; conducting protocol driven studies; maintaining correspondence with Sponsors; consulting with clients; writing/reviewing reports to be included in sponsor’s IND submission package; responding to Sponsor and in-house Quality Assurance audit reports; participating in scientific meetings; making presentations; coordinating site visits; and assisting Sales, Marketing and Customer Services.
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Principal Scientist, Drug TransportersXenotech, Llc May 2014 - Apr 2016Head of drug transporter department. Consult clients on drug transporter studies. Serve as manager of multiple nonclinical, drug transporter-related contract studies. Manager and mentor team members for individual development. Job responsibilities include preparing protocols and cost estimates; designing, scheduling, and conducting protocol driven studies; processing and reviewing data; troubleshooting technical problems; maintaining correspondence with Sponsors; writing Standard Operating Procedures (SOPs) and reports; responding to Sponsor and in-house Quality Assurance audit reports; participating in scientific meetings; making presentations; coordinating site visits; actively participating in research and development; and providing inter-department support, when needed.
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Senior Scientist, Drug TransportXenotech, Llc Jan 2012 - Apr 2014Serve as a study director of multiple nonclinical, drug transporter-related contract studies. Job responsibilities include preparing protocols and cost estimates; designing, scheduling, and conducting protocol driven studies; processing and reviewing data; troubleshooting technical problems; maintaining correspondence with Sponsors; writing Standard Operating Procedures (SOPs) and reports; responding to Sponsor and in-house Quality Assurance audit reports; participating in scientific meetings; making presentations; coordinating site visits; and providing inter-department support, when needed.
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Senior Scientist, Drug MetabolismXenotech, Llc Jan 2007 - Dec 2011Lenexa, KsServed as a study director/lead scientist of multiple nonclinical, drug metabolism-related contract studies in compliance with Good Laboratory Practices (GLP). Job responsibilities included preparing protocols and cost estimates; designing, scheduling, supervising and conducting protocol driven studies; processing and reviewing data; troubleshooting technical problems; training level one, level two and research scientists; maintaining correspondence with Sponsors; writing Standard Operating Procedures (SOPs) and reports; responding to Sponsor and in-house Quality Assurance audit reports; participating in scientific meetings; making presentations; coordinating site visits; coordinating the day-to-day activities of several scientists or, on an interim basis, the drug metabolism department; and providing inter-department support, when needed.
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Research Scientist, Drug MetabolismXenotech, Llc Dec 2001 - Dec 2006Lenexa, KsServed as an analyst of multiple drug metabolism studies metabolism studies. Served as a study director/lead scientist of multiple nonclinical, drug metabolism-related contract studies in compliance with Good Laboratory Practices (GLP). Job responsibilities included preparing protocols and cost estimates, designing, scheduling, supervising and conducting protocol driven studies, processing and reviewing data, troubleshooting technical problems, training level one and two scientists, maintaining correspondence with sponsors and writing Standard Operating Procedures (SOPs) and reports.
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Scientist Ii, Drug MetabolismXenotech, Llc Jan 2000 - Nov 2001Lenexa, KsWith minimum supervision, conducted drug metabolism-related biomedical research by performing the following duties in compliance with Good Laboratory Practices (GLP) regulations. Conducted biomedical research including preparing chemical reagents and HPLC mobile phase reagents, biochemical assays and in vitro incubations of drugs and new chemical entities. Designed experiments. Maintained appropriate logs and records. Processed and reviewed data. Maintained HPLC and wet chemistry laboratories and equipment. Wrote standard operating procedures with moderate supervision. Assisted in the preparation of reports. Corresponded with clients regarding routine matters.
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Scientist I, Drug MetabolismXenotech, Llc Jan 1999 - Dec 1999With moderate supervision, conducted drug metabolism-related biomedical research by performing the following duties in compliance with Good Laboratory Practices (GLP) regulations. Conducted bio-medical research including preparing chemical reagents and HPLC mobile phase reagents, biochemical assays and in vitro incubations of drugs and new chemical entities. Designed routine experiments. Maintained appropriate logs and records. Processed and reviewed data.
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Laboratory TechnicianP.Q. Corporation Jan 1997 - Jan 1998Analyzed all plant materials according to ISO 9002 procedure. Job responsibilities included analyzing and approving all products made for consumers, preparing bulk solutions, setting up new instruments for plant use, creating new instrument manuals and procedure manuals for new employees, training new employees, and preparing standards.
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Laboratory AssistantBaker University Jan 1994 - Jan 1995Responsible for preparing bulks solutions and experiments for students in General Chemistry I and II. Assisted students in problem solving and troubleshooting.
Andrea Wolff Skills
Andrea Wolff Education Details
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Biology And Chemistry
Frequently Asked Questions about Andrea Wolff
What company does Andrea Wolff work for?
Andrea Wolff works for Xenotech
What is Andrea Wolff's role at the current company?
Andrea Wolff's current role is Director at XenoTech.
What is Andrea Wolff's email address?
Andrea Wolff's email address is aw****@****llc.com
What schools did Andrea Wolff attend?
Andrea Wolff attended Baker University.
What skills is Andrea Wolff known for?
Andrea Wolff has skills like Glp, In Vitro, Drug Metabolism, Hplc, Assay Development, Drug Development, Drug Discovery, Adme, Cro, Sop, Pharmacokinetics, Dmpk.
Who are Andrea Wolff's colleagues?
Andrea Wolff's colleagues are Hank Kapka, Krystal Gilligan, Jackie Glidewell, Megan Simmons, Leah Logan, Brooke Steenhard, Phd, Arash Skakibaie.
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Andrea Wolff
Chandler, Az
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