NewEinstein ED Assistant Nurse Manager Nights Jefferson HealthEinstein ED Assistant Nurse Manager NightsHaddonfield, NJJefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. Thomas Jefferson University, home of Sidney Kimmel Medical College, Jefferson College of Nursing, and the Kanbar College of Design, Engineering and Commerce, dates back to 1824 and today comprises 10 colleges and three schools offering 200+ undergraduate and graduate programs to more than 8,300 students.
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.
NewClinical Research Coordinator (Full Time) Tandem Intermediate LLCClinical Research Coordinator (Full Time)Somers Point, NjKnowledge, Skills, and Abilities * - Strong leadership and communication skills * - Exceptional organizational and multitasking abilities * - High attention to detail and commitment to regulatory compliance * - Ability to work independently and collaboratively in a multidisciplinary environment * - Strong time management and operational efficiency skills * - Proficiency with office equipment and study-specific systems * - Ability to maintain strict confidentiality * Required Experience & Qualifications * - Education: Bachelor's degree in a related field * - Experience: Minimum of two (2) years of clinical research or clinical trial management experience * - Preferred Credentials: Medical certification or licensure (e.g., MS, LPN, RN) * - Phlebotomy: Prior experience performing blood draws and handling biological specimens required PI4f8b0e84d8a1-29400-41203296 The CRC serves as the primary owner of study coordination, documentation, data management, and sponsor communication, supporting compliant trial execution from study start-up through close-out.
Clinical Research Coordinator II CenExelClinical Research Coordinator IIMarlton, New JerseyRecently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
NewClinical Research Coordinator I CenExelClinical Research Coordinator IMarlton, New JerseyResponsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
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.
Clinical Research Coordinator II Hassman Research Institute, LLCClinical Research Coordinator IIMarlton, NJ$26.24–$33.51 / hourPart timeRecently acquired by BayPine Capital Partners, our research sites provide unparalleled medical and scientific support in the design and execution of clinical trials. Responsible for coordinating all aspects of clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies.
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 DedicatedNJ$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.
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 CorpDirector, Clinical Research Scientist IAIWilmington, DEContribute to the development of program strategy for assigned compoundsprograms including participation in the preparation of clinical development plans Drafting and review of clinical scientific documents such as IND amendments Investigator Brochures Annual Reports and other Health Authority submissions. By 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.
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.
Senior Director Clinical Research Scientist Incyte CorpSenior Director Clinical Research ScientistWilmington, DEregulatory interactions governance Preferred Qualifications All Levels Experience in clinical pharmacology immunology or oncology Strong scientific curiosity and a proactive question-driven mindset Ability to present complex data clearly and effectively Additional Information Willingness to travel up to 20 as needed reasonable accommodations available Disclaimer The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. By 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.
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.