Research associate ii - united states, boulder

** 3 research associates w/ with analytical molecular biology technologies (qpcr, rtpcr), experience with digital pcr a plus- exp w/ data entry and analysis – bs molecular biology, chemistry or biology & 2 + years

duration: 6 months

the digital biology group is a multidisciplinary team focused on developing innovative products using our core partitioning technology. our ddpcr systems have enabled scientists around the world to make impactful discoveries in the life sciences and healthcare. our mission is to continue creating and providing new tools to scientists that will facilitate more discoveries and advances in research.

we currently have an opening for a research associate in the product development team, working on a novel ddpcr platform. if you relish the challenge of building new products and are passionate about the development of new analytical technologies, please reply to this job posting.

this position will be part of a team responsible for development of reagents associated with an advanced molecular biology instrumentation platform. the ideal candidate will have experience with molecular biology laboratory techniques, with an emphasis on pcr, foundation in relevant scientific knowledge

assists in planning experimental protocols with guidance from senior team members independently conducts well controlled molecular biology experiments makes detailed observations, and analyzes data with guidance from senior team members bachelor’s degree in related discipline (biochemistry, chemistry, biology, chemical engineering, etc.) 2+ years of related experience or equivalent combination of education and experience. foundational knowledge of related scientific discipline e.g., biochemistry, biology, and chemistry relevant to the position experience with experimental design experience with analytical molecular biology technologies (qpcr, rtpcr), experience with digital pcr a plus experience with microsoft office suite of products, specifically word, excel and powerpoint familiarity with computer techniques and software used for data entry and analysis (excel, python, matlab , jmp or other data analysis platform experience preferable) utilize clinical knowledge to improve clinical compliance on internal processes and at external clinical sitesmaintain responsibility for clinical study activities at multiple clinical sites for several ongoing clinical studiesprovided for clinical services deliveryexecute clinical research studies with human subjects at mchsarising during clinical trial executiongoverning the conduct of clinical trials no relocation assistanceassist clinical teams in evaluating the progress of vendor contracts as the clinical programprovide leadership in clinical trial activitiesgenerate clinical evidence for selected productsmaintain ongoing clinical research site correspondence and site filesconduct clinical visits and attend patient treatment days as needed to support the clinical projectproviding analyzes for robust clinical claim supportsupporting clinical research or similar experience in a medical/scientific areaprovide coverage to clinical contact telephone linesprovide clinical input to project risk assessmentsobserve, monitor and report clinical trends by keeping current with clinical results for assigned sitesmanaging the planning, implementation, and tracking of clinical monitoring processes, administration of clinical trials and maintaining an overview of the clinical trialsensure clinical protocols and statistical methods meet sound and efficient statistical and clinical trial methodologiesprovide support to the clinical affairs staff by monitoring data and ensuring clinical study documentation beprovide clinical administrative support to the study teams

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