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Senior Study Directors must have at least 2 years' experience at the Study Director level or equivalent experience where preclinical efficacy testing is the primary focus of the position.
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The position will primarily support the new HEALthy Brain & Child Development Study (PIs Laurie Wakschlag & Elizabeth Norton, Scientific Project Director Renee Edwards), a national, consortium study looking at the impact of prenatal substance exposure and other adverse and protective factors on infant brain and behavioral development.
$22.52 - $28.15 an hourFull-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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This research position is for a full-time Research Study Coordinator to assist PI Gallo in coordinating a newly funded NIH research study. The Research Study Coordinator will work closely with the lab PI and students in the lab to implement computerized cognitive experiments in younger and older adults.
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Responsibilities include establishment of, and adherence to, non-clinical study timelines, monitoring of study conduct at the TPO via communication with the Study Director and/or onsite observation, and real time communication with the Toxicology ADME/ToxPath/Drug Disposition (ATP) team throughout study planning, execution and reporting.
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Plan, conduct, and lead complex clinical study audits (Sponsor, Investigator Sites and Clinical Suppliers) (either remote or on site) in accordance with all applicable regulations, standards, guidance, and the established procedures, maintaining a high standard of service delivery that ensures effective customer relationships.
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Experience of working under own initiative and in planning and prioritizing workloads University or technical college degree or equivalent qualification in relevant sciences such as: Medicine, Pharmacy, Chemistry, Biochemistry, Biology, Microbiology, Biotechnology, Health Technology, Toxicology, Physics, Biophysics, Material Science Biomedical Engineering, Mechanical, Electrical or Electronic Engineering, Computer & Software Technology, Human Physiology, Nursing, Quality Management.
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As the Research Study Technician 3, you will review and comply with all policies, guidelines and operating procedures pertaining to the animal care and research program. Research Study Technician 3.
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Complete audits to assess accuracy and quality of scientific data submitted to the regulatory agencies in support of in vivo medical devices and in vitro diagnostic devices' application. QualificationsTo be considered for this role, you’ll require a minimum of 5 years of professional experience in relevant field of healthcare products or related activities e.g.:Work in medical devices industry and/or in vitro diagnostic devices(preferred) or closely related industries (e.g., pharmaceutical industry) such as research and development, manufacturing, quality management, regulatory affairs.
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Join us and discover an environment in which you’ll be supported to learn, grow and become your best self. Manage audit observations and audit reports through the internal audit database and CAPA process.
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We believe that the human element, across our global teams, is what allows us to continually evolve. We have an excellent new opportunity for a Medical Device Lead Auditor to join our global organization.
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The Study Director - Liquid Chromatography Mass Spectrometry (LCMS), is responsible for scientific, administrative, regulatory and project management for clinical and pre-clinical bioanalytical studies.
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Minimum of 4 years’ experience in a contract research laboratory, pharmaceutical or biotechnology industries, or equivalent experience considered for Study Director level. Applicants with less experience may be considered for an Associate Study Director position.
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We have an exciting opportunity for a Toxicology Study Director / Pharmaceutical and Medical Device. SUMMARY The Toxicology Study Director is responsible for managing the design, execution, and reporting of studies, meeting all scientific, regulatory and client requirements.
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Our Program for Comparative Research is looking for a GLP Study Coordinator, which will ensure Good Laboratory Practices (GLP) are being utilized in IND enabling in vivo studies. Keywords: Study Coordinator, Location: Philadelphia, PA - 19122 , PL: 593241638.
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Wages under this position are paid from Work Study awards administered by the CSN Financial Aid Department. Disclaimer Offer and acceptance of a Work Study Award are not a guarantee of employment.
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Title: study director Company: Science Solutions Recruitment
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