Research / Sr. Research Investigator, Quantitative Pharmacology Incyte CorpResearch / Sr. Research Investigator, Quantitative PharmacologyWilmington, DEBy 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 Incytes data protection officer and your supervisory authority if applicable. Through the discovery development and commercialization of proprietary therapeutics Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology Oncology and Inflammation and Autoimmunity Headquartered in Wilmington Delaware Incyte has operations in North America Europe and Asia.
Research Regulatory Coordinator, Full Time, Virtua Health IncResearch Regulatory Coordinator, Full Time,Voorhees, NJ$26–$39.11 / hourConducts administrative and regulatory activities related to support the conduct of clinical trials and daily operation of the clinical research program assisting with study implementation, study close-out, follow-up, and the facilitation of communication between study sites, principal investigators, sub-investigators, clinical research team and IRB. Prepares and processes all regulatory documentation to support the Clinical Research Program in managing IRB documents and protocols for the IRB, central IRB, external IRBs and all applicable regulatory review committees including new submissions, continuing reviews, amendments, adverse events, and reportable events.
Clinical Research Coordinator II- Orthopedics Nemours FoundationClinical Research Coordinator II- OrthopedicsWilmington, DEThe Clinical Research Coordinator II coordinates, implements and completes clinical research studies and/or clinical trials in the Orthopedics 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. Coordinates IRB submissions for assigned studies, maintains regulatory documents during conduct of study; develops and utilizes study participant and family teaching tools for study purposes; interfaces with representatives of sponsoring agencies.
Clinical Research Associate (M/W/D) - Region: Stuttgart, Heilbronn, Heidelberg Bristol Myers SquibbClinical Research Associate (M/W/D) - Region: Stuttgart, Heilbronn, HeidelbergStuttgart, DERemoteEach of us is empowered to apply our individual talents and unique perspectives in a supportive culture, promoting global participation in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues. Working knowledge of ICH/GCP Guidelines and applicable local laws and regulations (that govern clinical trials, with the ability to apply regulatory requirements to ensure compliance in clinical research activities (Analytical thinking/critical thinking skills.
Clinical Research Technologist II- Biobank Nemours FoundationClinical Research Technologist II- BiobankWilmington, DEEssential Functions: Responsible for processing various biological specimens (blood and body fluid, tissue, bone marrow, etc.) and utilizing databases for specimen tracking and storage, following laboratory protocols and SOP's. This individual will conduct routine specimen processing and shipping for both internally and externally funded projects of interest to the laboratory, including plasma/serum processing, mononuclear cell extraction, tissue culture, specimen data entry, and accessioning.
Quality Assurance And Research Education Coordinator Nemours FoundationQuality Assurance And Research Education CoordinatorWilmington, DEThe Research Quality Assurance and Education Coordinator supports compliance with research protocols, federal and state regulations, ICH:GCP guidelines, and institutional policies. This position conducts QA monitoring, provides education, and promotes high-quality research practices across Nemours Biomedical Research.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedNewark, DE$71,900–$189,000 / yearEnsure 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.
Pediatric Scientist, Autism Research Nemours FoundationPediatric Scientist, Autism ResearchWilmington, DEThe Research Scientist will join a multidisciplinary team that includes faculty from psychology, developmental medicine, psychiatry, neurology, social work, nursing, and applied behavior analysis, as well as colleagues who are autistic and/or caregivers. Provide clinical services as a minor part of this role, which might include autism diagnostic services, individual/group therapy, and/or supervising trainees, e.g., externs, residents, and/or fellows who rotate through the center.
Research Scientist - Invitro QPS Holdings LLCResearch Scientist - InvitroNewark, DEQPS' 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. As the Principal Investigator, incumbent will fill the role of Technical Leader, and be responsible for completing portions of/entire, projects, and providing quality and timely results, as well as collaborating and communicating with Clients, QPS management, and external resources.
Clinical Research Associate - Full-Service Syneos Health IncClinical Research Associate - Full-ServiceDETogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health IncExperienced Clinical Research Associate - Sponsor DedicatedDETogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Biostatistician- Research Nemours FoundationBiostatistician- ResearchWilmington, DEThis hybrid role focuses on collaboration with researchers in the Delaware Valley region, working alongside clinical investigators, physicians, and scientists in multidisciplinary research environments. The Biostatistician will play a pivotal role in advancing scientific discovery and improving health outcomes for children through support of diverse clinical studies.
Endowed Chair Of Pediatric Sickle Cell Disease Research Nemours FoundationEndowed Chair Of Pediatric Sickle Cell Disease ResearchWilmington, DEThe 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. Collaborate with the multidisciplinary SCD clinical team to ensure superb clinical care and regularly participate in the administrative activities of the Division and the department, as appropriate.
Director, Clinical Research Scientist IAI Incyte CorporationDirector, Clinical Research Scientist IAIWilmington, 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). Overview: Incyte is a biopharmaceutical company focused on the discovery development and commercialization of novel medicines to meet serious unmet medical needs in oncology and inflammation and autoimmunity.
Senior Research Scientist IRESenior Research ScientistWilmington, DelawareCharacterize purified proteins and antibodies using a broad range of biochemical and biophysical techniques, including analytical SEC/HPLC, SDS-PAGE, intact-mass analysis where applicable, DSF/thermal shift assays, BLI, SPR, and other analytical assays. PhD in Biochemistry, Biophysics, Protein Chemistry, Molecular Biology, Structural Biology, or a related field with at least 2 years of relevant experience, or a Master's degree with at least 5 years of relevant experience in drug discovery, biotechnology, pharmaceutical research, or an academic laboratory.
Research Accountant University of DelawareResearch AccountantNewark, DEUnder the general direction of the Assistant Director, Research Accounting and Billing, the Research Accountant manages and administers the post-award administration of assigned externally funded sponsored programs and other restricted funds to ensure compliance with governing federal, state, sponsor, UD requirements and generally accepted accounting principles. Context of Job: The Research Office manages approximately $307 million in annual research expenditures associated with over 2,300 sponsored research projects and is responsible for central research administration of all sponsored contracts and grants awarded to the University of Delaware (UD).
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.
Director, Clinical Research Christiana Care Health SystemDirector, Clinical ResearchWilmington, DE$121,180.80–$193,897.60 / yearServes as the Research Institutes liaison with ChristianaCare's Center for Strategic Information Management (CSIM) and responsible for ensuring the Research Institutes data processes, procedures, and permissions are met pre and post EPIC implementation. PRINCIPAL DUTIES AND RESPONSIBILITIES: Responsible for oversight of the Research Institutes portfolio of research projects and related programs ensuring that all research is scientifically rigorous, clinically relevant, ethically sound and meet all institutional, state and federal rules, policies, and regulations.
NewSenior Research Scientist ICON PlcSenior Research ScientistWilmington, DECharacterize purified proteins and antibodies using a broad range of biochemical and biophysical techniques, including analytical SEC/HPLC, SDS-PAGE, intact-mass analysis where applicable, DSF/thermal shift assays, BLI, SPR, and other analytical assays. PhD in Biochemistry, Biophysics, Protein Chemistry, Molecular Biology, Structural Biology, or a related field with at least 2 years of relevant experience, or a Master's degree with at least 5 years of relevant experience in drug discovery, biotechnology, pharmaceutical research, or an academic laboratory.