Associate Research Scientist

Smithers PDS LLC (Pharmaceutical Development Services) brings new drugs to market by providing pre-clinical and clinical services for all phases of drug development. PDS works with customers to develop new methods, validate existing methods, as well as performing the assays necessary to analyze samples from patients on more than 100 clinical trials currently in different phases of the FDA regulated drug approval process. Our expert scientists perform large molecule bioanalysis, assay development, validation, and sample analysis at our GLP, GCP, and CLIA compliant laboratories.Smithers is seeking a talented Associate Research Scientist with expertise in bioanalytical assays (PK, ADA, Nab). The individual will be responsible for design, development and feasibility of new assays.This position is salaried and is classified as an exempt position. Exempt employees typically work 40 hours or more to adequately perform their responsibilities. Extended work hours may be necessary to support the business in meeting client deliverable commitments.The salary range for the role is $75,000 - $100,000 per year commensurate with experience and qualifications. Smithers PDS has a comprehensive health insurance package including a choice of 3 medical plans, dental, vision, 401K retirement plan and PTO.The Qualifications For This Role AreBA/BS in Biological or Physical Sciences and at least 3 - 5 years of relevant experience, MS in relevant field and at least 1-2 years of experienceUnderstanding of bioanalytical assays (various design and platforms)Experience supporting method validation studiesExperience with assay troubleshootingAbility to assist with training and provide technical guidance to more junior scientists as neededPrior CRO and GLP, GCP, and/or CLIA experience a plusExperience with automated laboratory systems a plusExperience in drafting SOPs a plusCorporate ResponsibilitiesAdherence to laboratory health and safety proceduresAdherence to Standard Operating Procedures (SOPs)Adherence to applicable company policies and guidelinesAdherence to federal and/or local regulations, as applicableEnsures appropriate reporting when there is reason to believe compliance with regulations, policies, guidelines, SOPs, quality, or other criteria are not being observed or enforcedEnsure materials and equipment are maintainedStandard RequirementsExcellent oral and written communication skillsProficient in advanced computer applications including MS Word, Excel, statistical programs, and Watson LIMS databaseAble to work independently and manage priorities, as well as operate as a team memberMust be solution oriented and open to inputMust be able to comfortably and successfully operate in a dynamic environment with shifting prioritiesMust be able to collaborate and partner at all levels of the organization to accomplish deliverables and meet quality standards#PharmaJobs