Clinical Research Associate Alexion Pharmaceuticals IncClinical Research AssociateWilmington, DEThe CRA works in close collaboration with local team members (Project Management Clinical Operations (PMCO), Study Start-Up (SSU) manager, Clinical Study Assistant (CSA) and other CRAs in Clinical Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner on a site level. Following quality issue processes by escalating systematic or serious quality issues, data privacy breaches, or ICH-GCP compliance issues to Global Study team, Local study team, Country Operations Line Management and/or Quality Group, representatives as required.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedNewark, DEEnsure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements. • Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation.
Clinical Research Coordinator NemoursClinical Research CoordinatorWilmington, DEFull timeNemours is seeking a Clinical Research Coordinator to join our Nemours Children's Health team in Wilmington, DE.The Clinical Research Coordinator coordinates, implements and completes clinical research studies and/or clinical trials in the Orthogenetics Department at Nemours Children's Hospital Delaware by assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent/consent forms, educating parents/participants, scheduling and conducting study procedures, collecting and recording study data, maintaining detailed study records, interfacing with study sponsors, participation in sponsor study monitoring visits, prepare for and participate in internal and external research audits, maintain various research databases. We deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships.
Senior Director Clinical Research Scientist Incyte CorporationSenior Director Clinical Research ScientistWilmington, DelawareBy accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte’s data protection officer, and your supervisory authority (if applicable). Depending on level, you will contribute to or lead early clinical development and clinical pharmacology programs, with increasing ownership, strategic influence, and cross-functional leadership at more senior levels.
Technical Associate - Research & Development TechDigital CorporationTechnical Associate - Research & DevelopmentNewark, DEQualifications: • B.S. or M.S. degree in Chemistry or related science, with at least three years of working experience in a laboratory setting with a focus on wet chemistry and analytical chemistry• 2+ years of experience with liquid chromatography (LC or HPLC) is highly desirable• Experience with GLP and/or working in a regulated environment such as the food / pharma industries would be beneficial• Experience writing technical and customer reports with keen attention to detail• Excellent communication skills and bias for teamwork necessary to succeed in a multifunctional, collaborative team environment• Excellent organizational skills with flexibility and a bias for action will be necessary for managing fast-changing project demands• Job is onsite Responsibilities: • Execution of a variety of projects and studies as needed including Client product dissolution tests, drug assays, and product stability studies• Analytical method development, operation, and maintenance of HPLC instrumentation• Independent and detail-oriented execution of general laboratory activities, including operation of pharmaceutical formulation equipment; formulation / preparation of samples and reagents; completion of routine laboratory experiements; operation, troubleshooting, maintenance, and calibration of instrumentation; developing and implementing new test methods for product development purposes• Candidate will be required to handle Schedule II pharmaceuticals, manage associated documentation, and participate in DEA audits• Meticulous documentation of laboratory procedures and data; maintenance of electronic databases, laboratory notebooks, and technical reports in accordance with Good Laboratory Practices (GLP) or equivalent• Maintaining a safe, clean laboratory environment with attention to lab housekeeping, including stocking of consumables / lab supplies and waste disposal• Active participation in work group team meetings to address safety, process improvement, problem solving, and other topics functional topics; additional project team participation as required.• Help with product development for the pharmaceutical job industryAnalyzing research articles and staying informed about recent product innovations to design experiments applicable to diverse product applications.
Clinical Study Administrator GTTClinical Study AdministratorWilmington, DEThis position serves as a key administrative contact for investigators, clinical research associates, and external partners while maintaining study documentation, electronic trial master files (eTMF), and regulatory documentation to ensure inspection readiness and compliance with ICH-GCP guidelines. The organization collaborates with international teams, investigators, and regulatory authorities to support high-quality clinical studies and deliver impactful therapies to patients worldwide.
Research Lab Manager- Biobank NemoursResearch Lab Manager- BiobankWilmington, DEFull timeAssists laboratory management to maintain the lab websites and social media presence, including regular updates and enhancements and assures that the labs technology remains current, evaluating programs and platforms and monitoring appropriateness and use. We deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships.
Adapted Care Clinical Coordinator NemoursAdapted Care Clinical CoordinatorWilmington, DEFull timeWe deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships. Create programs and maintain education tools and resources; Develop plan to address ongoing training that reflect changes in best practice and population culture, SIM opportunities, etc.
Sr. Clinical Trials Manager Agilent Technologies IncSr. Clinical Trials ManagerDEMonitor and review study budget and data management activities, such as PRF development, training, and facilitating query resolution with proper documentation • Support monitoring efforts by setting quality and compliance goals by overseeing and approving study monitoring plans, may review, suggest edits and approve monitoring trip reports • Contribute to contract review and negotiations with outside vendors and study sites or laboratories • Mentor CTMs and CRAs • Demonstrate an ability to influence others to achieve positive results and collaboration through diplomacy and respect for others, appropriate prioritization and facilitation of the decision-making process Qualifications Qualifications: • Bachelors degree or higher, or equivalent credentials • Knowledge of GCP, ICH guidelines, and other clinical regulatory requirements • Strong interpersonal skills (verbal and written), organizational, and prioritization skills, able to communicate at multiple levels of an organization and with sponsors/clients. Primary Responsibilities (all levels): • Manage, design and implement all clinical operational aspects of IVD clinical trials from inception through close-out • Serve as main point of contact for internal and external study stakeholders; effectively communicating, collaborating, managing escalation of issues, where necessary, as well as participating and leading internal and external study meetings • Identify, evaluate, and oversee qualification and contracting for study investigators, study sites, CRO and/or vendor management for the study, where applicable • Develop or assist in the development of study-related plans and documents including protocols, informed consent forms, monitoring plans, case report forms, training plans and engagement materials • Ensure trial master file (TMF/eTMF) is established, current, and maintained per ICH E6.
Endowed Chair of Pediatric Sickle Cell Disease Research NemoursEndowed Chair of Pediatric Sickle Cell Disease ResearchWilmington, DEFull timeWe deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships. The Endowed Chair in SCD Research will report to and assist the Division Chief in resource planning, promotion of research and scholarly activity, and exploration of innovative funding opportunities for SCD research.
Vice Chair of Pediatric Anesthesiology Research and Program Development NemoursVice Chair of Pediatric Anesthesiology Research and Program DevelopmentWilmington, DEFull timeWe deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships. Job Summary: The Department of Anesthesiology and Perioperative Medicine at Nemours Children's Hospital, Wilmington, DE, is seeking a highly motivated and dynamic leader to serve as the Vice Chair for Research and Programmatic Development in Pediatric Anesthesiology.
Research Scientist- Remote Community Health Center IncResearch Scientist- RemoteDERemoteThe system delivers primary care to more than 150,000 patients in Connecticut, and extends access to specialty care for more than 2.5 million individuals across the U.S. It is a national accrediting body for organizations training advanced practice providers, and offers accredited education and training for Medical Assistants in multiple states. As an incubator for new ideas in areas including social justice, the environment, and social determinants of health, the MWHS is addressing challenges faced by providers caring for underserved communities, creating innovative and impactful initiatives led by nationally and internationally recognized experts.
Research Intern NemoursResearch InternWilmington, DEFull timeThe Biomedical Research, Innovation, and Translation in Extracorporeal Therapies (BRITE) Lab at Nemours Children's Hospital is a multidisciplinary team that combines clinical medicine and bioengineering to develop technologies to improve the outcomes for pediatric patients on extracorporeal life support (ECLS). We deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships.
Research Program Director of Environmental Health and Safety NemoursResearch Program Director of Environmental Health and SafetyWilmington, DEFull timeWe deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships. The position provides support and guidance in the development and implementation of institutional and laboratory/protocol-specific procedures and protocols, as well as conducting hazard assessments and responding to emergencies involving hazardous materials.
Research Scientist NemoursResearch ScientistWilmington, DEFull timeResearch activities include designing and fostering collaborative and independent research projects related to neuroscience and neurologic disease, supervision of postdoctoral associates, technicians and students, obtaining and coordinating external funding, and disseminating research in the form of manuscripts and conference presentations. We deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships.
Licensed Clinical Social Worker (LCSW) Gotham Enterprises LtdLicensed Clinical Social Worker (LCSW)Wilmington, DE$115,000–$120,000You will provide virtual sessions, assess client needs, and help clients move through clinical social work, mental health counseling, case-informed care, and client advocacy with care, structure, and realistic goals. · Master's degree in a relevant behavioral health field appropriate for Licensed Clinical Social Worker licensure.
Global Head of R&D & Clinical Development Sourcing Incyte CorpGlobal Head of R&D & Clinical Development SourcingWilmington, DEThis leader partners closely with Clinical Operations R&D Leadership Development Operations Biometrics Regulatory Quality and Finance to ensure the organization secures best in class CROs service providers technology platforms and scientific suppliers that enable speed quality and innovation in the drug development lifecycle. This role oversees a team of category leads and sourcing managers supporting the end to end value chain for preclinical research clinical operations biometrics scientific services and external development partnerships.
Clinical Pharmacy Specialist (General Pediatrics/Solid Organ Transplant) NemoursClinical Pharmacy Specialist (General Pediatrics/Solid Organ Transplant)Wilmington, DEFull timeEssential Functions: Evaluates medication orders for accuracy using sound principles, accounting for pharmacology of the drug, pharmacodynamic and pharmacokinetic variations in drug absorption, distribution, metabolism, and elimination with responsibility for establishing and continually improving the delivery of pharmaceutical care to patients within areas of direct responsibility and assisting others in the department with the same. Provides clinical support for multidisciplinary committees, including the Pharmacy and Therapeutics Committee, through the development of materials to support clinical evaluation of drugs, procedures, and processes including the coordination and reporting of adverse drug reaction reporting, pharmacist interventions and other quality initiatives, within areas of direct responsibility.
Ambulatory Pediatric Clinical Pharmacy Specialist (Hematology/Oncology) NemoursAmbulatory Pediatric Clinical Pharmacy Specialist (Hematology/Oncology)Wilmington, DEFull timeWe deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships. This pharmacist will practice as an integral member of the multidisciplinary care team, partnering closely with physicians, advanced practice providers, nurses, and the pharmacy staff to ensure safe, effective, and evidence ‑ based medication management.
Clinical Fraud Investigator II Elevance Health IncClinical Fraud Investigator IIWilmington, DEMinimum Requirements: Requires an Associate Degree in Nursing and/or current certification as a Certified Professional Coder (AAPC or AHIMA) and minimum of 4 years related experience, including minimum of 1 year experience in a Clinical Fraud and Abuse Investigation area; or any combination of education and experience, which would provide an equivalent background. We are a Fortune 25 company with a longstanding history in the healthcare industry, looking for leaders at all levels of the organization who are passionate about making an impact on our members and the communities we serve.
Clinical Pharmacist (Outpatient Pharmacy), Casual/PRN NemoursClinical Pharmacist (Outpatient Pharmacy), Casual/PRNWilmington, DEPart timePreviews and interprets medications orders for accuracy using sound principles, accounting for pharmacodynamic and pharmacokinetic variations in drug absorption, distribution, metabolism, and elimination with responsibility for establishing and continually improving the delivery of pharmaceutical care to patients within areas of direct responsibility and assisting others in the department with the same. Provides specialized pharmaceutical services to improve drug usage and therapeutic outcomes including advising physicians and practitioners on issues concerning drug therapy, the inherent toxicity of drugs, drug-drug, drug-food interactions, and side effects, as well as assisting in the prescribing of appropriate doses.
Clinical Nurse Supervisor NemoursClinical Nurse SupervisorWilmington, DEFull timeWe deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships. Initiates cost-effective and appropriate quality care by: Reviewing and adjusting unit assignment of staff in collaboration with Nurse Managers/Charge Nurses to insure adequate coverage of all patient care units in a cost effective manner.
Clinical Pharmacy Specialist - Emergency Department NemoursClinical Pharmacy Specialist - Emergency DepartmentWilmington, DEFull timeNemours is seeking a full‑time Pediatric Emergency Department (ED) Clinical Pharmacy Specialist to join our highly collaborative and mission‑driven team at Nemours Children's Hospital, Wilmington, DE.NCH‑DE is a multi‑specialty, freestanding pediatric hospital and the only ACS‑verified Pediatric Level I Trauma Center in the state of Delaware. We deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships.
Clinical Pharmacist (Evening Shift) NemoursClinical Pharmacist (Evening Shift)Wilmington, DEFull timePreviews and interprets medications orders for accuracy using sound principles, accounting for pharmacodynamic and pharmacokinetic variations in drug absorption, distribution, metabolism, and elimination with responsibility for establishing and continually improving the delivery of pharmaceutical care to patients within areas of direct responsibility and assisting others in the department with the same. Provides specialized pharmaceutical services to improve drug usage and therapeutic outcomes including advising physicians and practitioners on issues concerning drug therapy, the inherent toxicity of drugs, drug-drug, drug-food interactions, and side effects, as well as assisting in the prescribing of appropriate doses.
Clinical Pharmacist (Evenings) NemoursClinical Pharmacist (Evenings)Wilmington, DEFull timePreviews and interprets medications orders for accuracy using sound principles, accounting for pharmacodynamic and pharmacokinetic variations in drug absorption, distribution, metabolism, and elimination with responsibility for establishing and continually improving the delivery of pharmaceutical care to patients within areas of direct responsibility and assisting others in the department with the same. Provides specialized pharmaceutical services to improve drug usage and therapeutic outcomes including advising physicians and practitioners on issues concerning drug therapy, the inherent toxicity of drugs, drug-drug, drug-food interactions, and side effects, as well as assisting in the prescribing of appropriate doses.
General Toxicology Associate Scientist MindlanceGeneral Toxicology Associate ScientistNewark, DEdiet, gavage, intraperitoneal, subcutaneous, etc.) • Body Weight, Food Consumption, holding for eye exams, other measurements and collection of biological samples as needed • Blood (tail vein) and urin collection, clinical observations, and other in-life study functions • Data collection manually and electronically (experience with Provantis Integrated Preclinical Software a plus) • Collecting, recording, documenting and reporting results with a high degree of accuracy and precision in a timely manner • Maintaining study data and related information in study files • Communicating effectively with Study Directors, peers, supervisors, and attending veterinarian • Understanding and following all relevant protocols, SOPs, GLPs, and safety guidelines • Learning and refining new laboratory skills and techniques • Assisting other technicians and completing other tasks as assigned Requirements • B.S. degree in animal science, biology or related science field with 2 years of relevant experience or an equivalent combination of education and work experience • Proficient in Microsoft Word and Excel and ability to learn other software/validated systems • Good communication (written and verbal) and interpersonal skills, an attention to detail, and commitment to quality • Ability to work safely under specific time constraints, prioritize workload, use time productively, and work well independently or in a team setting Physical Demands • Employees must be able to lift, move, manipulate, and/or hold heavy objects up to 50 pounds. Please note: If the employee had visited another animal facility on the same day as work, has had contact with companion-/pet-/wild-rodents, or had contact with snakes/reptiles/birds of prey that are fed rodents, the employee must shower and have a complete change of clothing prior to entering *** Agriscience’s animal vivarium.
Associate Director, Implementation Science AstraZeneca PlcAssociate Director, Implementation ScienceWilmington, DE$150,098.40–$225,147.60 / yearp>The Associate Director, Implementation Science is a strategic role within the US Evidence function, accountable for supporting the design and deployment of practice-change interventions that advance a data-enabled mindset shift, address clinical inertia, and accelerate adoption of evidence-based medicine (EBM) and Guideline-Directed Medication Therapy (GDMT) within assigned therapeutic areas. Reporting to Senior Director within the US Evidence Implementation Science team, the Associate Director is deployed flexibly across therapeutic areas based on portfolio priorities, working under the direction of senior team members to drive transforming-care initiatives that strengthen the clinical and economic value proposition of AstraZeneca's products in alignment with US brand strategy.
Director / Associate Director Companion Diagnostics Lead, Translational Sciences Incyte CorpDirector / Associate Director Companion Diagnostics Lead, Translational SciencesWilmington, DEKey duties include Serve as subject matter expert in CDx development process from concept to commercialization Lead selection and management of diagnostic partners Monitor assay analytical and clinical performance evaluation activities Author CDx related parts across documents Ensure CDx representation in cross-functional teams Serve as alliance and project manager between Incyte and key diagnostic partners Generate and review new project agreements as needed Manage and maintain CDx budget for projects Track and approve milestones for each project Lead Joint project team JPT meetings with alliance partner Supervise validation and implementation of clinical trial assay CTA at testing laboratory Maintain alignment between diagnostics partner and testing laboratory Ensure timelines are met Oversee operational aspects of clinical implementation Ensure compliance with regulatory and ethical guidelines Develop and apply expertise in regulatory requirements for CDx across regions US FDA EU IVDR etc Supervise Incyte review of CDx documentation such as clinical study performance plans CPSP Instructions for Use etc Ensure creation and review of informed consent CPSP and country submissionsresponses are timely and compliant Develop and Maintain Expertise in Delivery of Companion Diagnostics Maintain relationships with key stakeholders Qualifications Minimal acceptable level of education work experience and competency Minimum BS Degree in a scientific discipline with 7 years of experience in the diagnostic andor pharmaceutical industry clinical studies. Job Summary Primary function Associate Director Companion Diagnostics Lead is a leadership role responsible for the development and implementation of clinical diagnostic plans including companion diagnostics CDx requirements within drug development programs.
Associate Quality Systems Specialist Charles River Laboratories International IncAssociate Quality Systems SpecialistNewark, DEIf you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com. Prepare written and signed records of all audits and inspections as required and may sign records as a trainee, countersigned by supervisor/trainer, documenting the performance of audits and inspections and reporting to management.
Associate Director Accugenix Operations Charles River Laboratories International IncAssociate Director Accugenix OperationsNewark, DE$145,000–$155,000 / yearOur Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. Must have a demonstrated track record of accomplishments with strategy and leadership in operational areas, technical knowledge of business process, implementation of cross-functional projects and TOC/Lean Manufacturing or process improvement techniques.
FSP Associate Scientist- Cell Culture (on-site) Thermo Fisher ScientificFSP Associate Scientist- Cell Culture (on-site)Wilmington, DelawareQualifications (Minimal acceptable level of education, work experience, and competency): BS degree within chemical engineering, biochemical engineering biology, molecular biology, biochemistry or cell biology and 1+ years of experience in an appropriate subject area or working towards relevant qualification. Essential Functions of the Job (Key responsibilities): Completes experiments for generating stable CHO cell lines expressing therapeutic antibodies, which include preparation DNA for transfection, conduct experiment in transfection, screening of transfected cells, as well as routine cell culture work.
Associate Director, International Regulatory Affairs Incyte CorporationAssociate Director, International Regulatory AffairsWilmington, DelawareThe Associate Director, International Regulatory Affairs works in collaboration with International Regulatory Affairs Lead to develop regulatory strategies with multi-functional teams and partners and ensures that International Regulatory Requirements for assigned products are complete. Provide appropriate regulatory strategies to support submission of marketing and life-cycle applications (may also include support of clinical trial applications/expanded access programs) in International Markets Provides regulatory support to inter-departmental project teams.
FSP Associate Scientist- Purification Process Sciences Thermo Fisher ScientificFSP Associate Scientist- Purification Process SciencesWilmington, DelawareWithin our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Associate Scientist- Cell culture Thermo Fisher ScientificAssociate Scientist- Cell cultureWilmington, DelawareWithin our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Associate Director, Marketing - Life Cycle Management/HCP Marketing AstraZeneca PlcAssociate Director, Marketing - Life Cycle Management/HCP MarketingWilmington, DEOversee the launch readiness and launch for future indications and LCM activities, including coordination across the cross functional team, ensuring dynamic strategic and tactical plan are built and aligned across the organization. Join us as Associate Director, Marketing in Wilmington, DE for the respiratory team, where you will play a pivotal role in channeling our scientific capabilities to make a positive impact on changing patients' lives.
Associate Director HCP Marketing, ATTR AstraZeneca PlcAssociate Director HCP Marketing, ATTRWilmington, DE$175,000–$205,000 / yearIn addition, our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles), to receive a retirement contribution (hourly roles), and commission payment eligibility (sales roles). Join us as a Marketing Associate Director, supporting our ATTR portfolio where your work directly shapes how we engage HCPs and advance understanding of a rare, serious form of amyloidosis caused by abnormal transthyretin proteins.
Toxicology Associate Scientist Net2SourceToxicology Associate ScientistNewark, DE$23–$25 / hourPlease note: If the employee had visited another animal facility on the same day as work, has had contact with companion-/pet-/wild-rodents, or had contact with snakes/reptiles/birds of prey that are fed rodents, the employee must shower and have a complete change of clothing prior to entering animal vivarium. • The employee will work regularly with live animals requiring the use of appropriate PPE to prevent exposure to allergens, biohazards, and/or test material hazards.
Inbound/Outbound Queue Associate - Behavioral Health CVS Health CorpInbound/Outbound Queue Associate - Behavioral HealthWork At Home-Delaware, DERemote$17–$31.30 / hourThis is a fully remote position and the following are some required Work from Home criteria which includes but is not limited to maintaining your own internet with approved speed requirements, secure workspace free from distractions, and successful completion of the training program. Strong customer service skills to coordinate service delivery including attention to customers, sensitivity to issues, proactive identification and resolution of issues to promote positive outcomes for members.
Associate Manager, Regulatory & Scientific Affairs International Flavors & Fragrances IncAssociate Manager, Regulatory & Scientific AffairsWilmington, DEli>Prepare, review, and submit regulatory dossiers and filings, including Generally Recognized as Safe (GRAS) notices, New Dietary Ingredient Notifications (NDINs), Product License Applications (PLAs), Master Files, and Chemistry, Manufacturing, and Controls (CMC) documentation. This role is part of global regulatory focus teams and partners closely with R&D, Quality, Commercial, Marketing, and Legal stakeholders to ensure regulatory compliance while enabling product development, manufacturing, and commercialization.
NewAssociate Actuary, Strategic Analytics Centene Corporation GroupAssociate Actuary, Strategic AnalyticsDERemote$87,700–$157,800 / yearp>Strategic Impact of the Role: We are seeking an entrepreneurial and innovative Associate Actuary to serve as a key strategic leader evaluating our highest-priority strategic initiatives - specifically, internal Quality and Affordability Initiatives (QAI) and external Value-Based Care (VBC) arrangements. Executive Translation: Act as a strategic communicator, translating highly complex actuarial methodologies and financial impacts into compelling, easily understood narratives for non-technical executive stakeholders.
Associate Scientist I - Bioanalytical dept QPS Holdings LLCAssociate Scientist I - Bioanalytical deptNewark, DEAs an Associate Scientist I, you will be a fully-supervised trainee, responsible for sample preparation by various extraction methods; analysis of drug and metabolites in biological samples to support preclinical and clinical drug development programs under GLP regulations; and recording study results and observations. QPS' Story: Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV Clinical Research services.
Associate Scientist I - TLM QPS Holdings LLCAssociate Scientist I - TLMNewark, DEp>QPS' Story: Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II - IV Clinical Research services. The Translational Medicine (TLM) department of QPS is comprised of three laboratory operations units: Biomarker Analysis (BMA), Gene & Sequence Analysis (GSA), and Immunobioanalysis (IBA).
Molecular Technologist I Charles River Laboratories International IncMolecular Technologist INewark, DE$21–$22 / hourOur Microbial Solutions business group has a comprehensive portfolio of endotoxin testing, microbial detection and microbial identification products and services is unlike any other, and has been purposefully designed to meet the complex and ever-changing needs of the industry. The Molecular Technologist 1 will process customer samples in the microbiology laboratory utilizing the various technology platforms including but not limited to bacterial 16S rDNA and fungal ITS2 sequencing, MALDI-TOF mass spectrometry and ribotyping.
Academic Program Coordinator University of DelawareAcademic Program CoordinatorNewark, DECONTEXT OF THE JOB: Under the limited supervision of the Business Administrator II, Department Chair, and Associate Department Chair in the Department of Kinesiology & Applied Physiology, the Academic Program Coordinator manages the administration of the department's undergraduate programs, serves as liaison with University faculty, sta, students, and o-campus organizations/contacts, and is responsible for the programs, department, and university policy applications. Coordinate undergraduate recruitment, outreach, communication campaigns, social media content, advising publications, admissions events, Convocation, workshops, and alumni relations efforts in partnership with departmental and University stakeholders.
NewImplant Control Coordinator II - Wilmington Christiana Care Health SystemImplant Control Coordinator II - WilmingtonWilmington, DE$22.29–$33.44 / hourIncredible Work/Life benefits including annual membership to care.com, access to backup care services for dependents through Care@Work, retirement planning services, financial coaching, fitness and wellness reimbursement, and great discounts through several vendors for hotels, rental cars, theme parks, shows, sporting events, movie tickets and much more! ChristianaCare is looking for a full-time Implant Control Coordinator II to provide support to the Clinical Supply Chain Manager and Perioperative Materials Supervisor in ensuring that all Periop Material is provided in an efficient and cost-effective manner to the CCHS surgical areas.
Materials Inventory Coordinator II - Surgical Materials Distribution - Wilmington Christiana Care Health SystemMaterials Inventory Coordinator II - Surgical Materials Distribution - WilmingtonWilmington, DE$19.84–$29.76 / hourli>Incredible Work/Life benefits including annual membership to care.com, access to backup care services for dependents through Care@Work, retirement planning services, financial coaching, fitness and wellness reimbursement, and great discounts through several vendors for hotels, rental cars, theme parks, shows, sporting events, movie tickets and much more! The Inventory Coordinator will provide support to the Clinical Supply Chain Manager and Perioperative Materials Supervisor in ensuring that all Periop Material is provided in an efficient and cost-effective manner to the CCHS surgical areas.