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Ability to obtain the DOT medical examiner certificate (Physical and Drug/Alcohol Screen). Maintain cleanliness of truck. This Knuckle Boom Truck Operator position is FT and offers competitive pay and a full benefits package to qualified candidates.
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This role is responsible to assist with overseeing all aspects of drug safety study operational activities from study start up to close out. This role assists with oversight of clinical trial safety operational vendor activities and supports all major tasks related to the management and best utilization of case processing activities in the Argus Safety Database, ensuring compliance with global clinical safety and PV regulations and Global Patient Safety (GPS) department procedures in all aspects of drug safety case processing and reporting.
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Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
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Ability to obtain the DOT Medical Examiner's Certificate (Physical and Drug/Alcohol Screen) Delivers and unloads materials to customers' satisfaction, Completes daily equipment pre-inspection, Records all merchandise that is returned by truck, assists in unloading material returned, Follows guidelines established by the Department of Transportation, Assists in maintaining good housekeeping in yard, Complies with all company policies and guidelines, Maintain cleanliness of truck.
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Certara is focused on the use of model-informed drug development to supplement or replace traditional drug development processes with in silico approaches which include modeling and simulation, clinical trial simulation, real-world evidence generation, paired with extensive drug development, regulatory and market access expertise.
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PhD degree in Pharmaceutics, Biology, Biochemistry, Biotechnology, Chemistry, Chemical Engineering with protein formulation and drug delivery development experience; or MS degree with 5+ years of experience; or BS degree with 10+ more years of experience.
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10+ years of experience in third-party risk management, cyber security, or related fields, with a focus on monitoring and testing. Leveraging your extensive experience in third-party risk management and cyber security, you will design strategies and processes to effectively assess our risk exposure, ensuring proactive identification of potential threats and vulnerabilities.
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Head of US, Global Real-World Evidence & Health Outcomes Research will lead the US team to deliver relevant, innovative and high impact evidence to meet the needs of external stakeholders such as health care professionals, scientific communities, Health Technology Assessment (HTA) and recommending bodies, patient and advocacy groups and other material stakeholders.
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As an Investigator, within Emerging Drug Delivery Platforms you will be responsible for identifying, evaluating, and supporting the implementation of the drug delivery capabilities needed by GSK to support a rapidly growing and diversifying patient centric portfolio.
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Experience in drug safety, pharmacovigilance, quality assurance and compliance requirements is desirable. MD/PharmD/PhD or equivalent with 10+ years of pharmaceutical/biotherapeutics industry experience.
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Collaborate with the Senior Manager, Accounting Operations, and other internal departments to design, document, implement, and monitor processes that establish internal controls, ownership, and accountability of involved parties related to cash & sales processing, master data management, procurement, inventory management.
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Frontage Laboratories Inc. is an award winning, publicly listed (HKSE), full-service CRO/Contract Research Organization operating over 25 state-of-the-art laboratories across the US, Canada and China, and growing over 30% YOY. Our core competencies include drug metabolism, pharmacokinetics/ pharmacodynamics (PK/PD), safety and toxicology, bioanalytical services, chemistry and manufacturing controls for drug development, and core laboratory services for clinical trials.
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Knowledge of the drug development process and clinical research methodologies including experience in clinical trial design, data analysis/statistics and data interpretation; knowledge of regulations, ICH/GCP, adverse event management.
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Drive a non-CDL straight body box truck (requires passing a DOT medical card exam). Emergency Response:The KWF Facilities and Maintenance Team Member is part of the KWF Emergency Response Team and must be responsive outside of regularly scheduled hours.
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Full Time Closing Front of House Team Member 2:00pm or 3:00pm - 11:30pm, 5 days, 40 hours, $18 per hourAt Chick-fil-A Malvern, our Vision is to create remarkable experiences by caring for our guests, caring for our community, and caring for each other.
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drug alcohol of truck driver jobs Title: cdl driver Company: Trimac Transportation in Phoenixville, PA
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