Clinical Research Associate (M/W/D) - Region: Stuttgart, Heilbronn, Heidelberg Bristol Myers SquibbClinical Research Associate (M/W/D) - Region: Stuttgart, Heilbronn, HeidelbergHeidelberg, 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 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.
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.
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.
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.
Associate Director Radiopharmaceutical Clinical Applications - Mid-Atlantic (NJ, PA, Washington DC, MD, DE) Lantheus Holdings IncAssociate Director Radiopharmaceutical Clinical Applications - Mid-Atlantic (NJ, PA, Washington DC, MD, DE)Bethany Beach, DERemote$163,000–$245,000 / yearIdentify, develop, and engage in long-term relationships with Key Opinion Leaders (KOLs) and Healthcare Providers (HCPs) in the assigned territory, including Nuclear Medicine Physicians, Radiologists, Radiation Oncologists, Technologists, Safety Officers, Health Physicists, Nursing Staff, and Advanced Practice HCPs at imaging facilities and medical centers. This role involves building and maintaining relationships with Key Opinion Leaders (KOLs) and Healthcare Providers (HCPs), providing advanced clinical and technical expertise, and ensuring the optimal use of our products in the clinical setting.
Associate Director, Clinical R&D QA US Incyte CorpAssociate Director, Clinical R&D QA USWilmington, DEAssist with the maintenance of the clinical Quality Management System including QA support for change control deviations reviewrevision of SOPs with ensuring continuous process improvement Stay abreast of clinical trial requirements ICH GCP and guidelines from other regulatory agencies for the management of clinical trials as appropriate. Be thoroughly familiar with assigned Incyte Compounds and protocol REQUIREMENTS Bachelors degree in a science or healthcare related discipline or similarly conferred degree from a university 5 to 7 years experience in a pharmaceutical or bio-pharmaceutical company in a GCP QA role or Clinical compliance role.
Associate Clinical Editor RELX Group plcAssociate Clinical EditorDelaware, DERemote$71,600–$119,400 / yearIf performed in Colorado, the base pay range is $71,600 - $119,400.If performed in Illinois, the base pay range is $75,200 - $125,500.If performed in Chicago, IL, the base pay range is $78,700 - $131,400.If performed in Maryland, the base pay range is $75,200 - $125,500.If performed in Ohio, the base pay range is $68,000 - $113,400. Responsibilities: Review, update, and revise assigned content based on scheduled and triggered review cycles, as well as customer needs and requests, and current events in health care such as guideline update under the guidance of a Clinical Editor.
Quality Assurance and Research Education Coordinator NemoursQuality Assurance and Research Education CoordinatorWilmington, DEFull timeParticipates in education of new team members as well as ongoing education of teams based on gaps identified through internal audits, sponsor monitoring visits, changes in regulations, departmental/corporate policies and other factors as determined by department leadership. 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.
Pediatric Nurse Practitioner or Physician Assistant, Research NemoursPediatric Nurse Practitioner or Physician Assistant, ResearchWilmington, DEFull timeThe incumbent will coordinate, implement and complete clinical research studies or clinical trials by assisting with IRB submissions, assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent, educating parents/participants, scheduling and conducting study procedures/examinations, collecting and recording study data, maintaining study records, interfacing with study sponsors, participation in sponsor study monitoring visits. 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.
Pediatric Scientist, Autism Research NemoursPediatric Scientist, Autism 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 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.
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 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.
NewPrincipal Carelon Research Biostatistician Elevance HealthPrincipal Carelon Research BiostatisticianWilmington, DE$136,000–$234,600 / yearThis researcher partners with investigators, research sponsors, academic institutions, and cross-functional project teams to design studies, develop statistical methodologies, oversee analytical execution, and communicate scientific findings that advance externally funded clinical research programs. Experience designing clinical research studies, developing sample size calculations, statistical analysis plans, outcome measures, and advanced statistical methodologies including survival analysis, causal inference, and experimental design preferred.
Pediatric Orthopedic Research Scholar - Orthoapedics Residency Program NemoursPediatric Orthopedic Research Scholar - Orthoapedics Residency ProgramWilmington, DEFull timeCollaborate with some of the most recognized and prolific thought leaders in the pediatric orthopedic profession, in an institution known for its scholarship in complex diagnoses such as: osteogenesis imperfecta, scoliosis, cerebral palsy and progressive neuromuscular conditions, skeletal dysplasia's (dwarfism), hip dysplasia, limb deformities, sports medicine, and more. 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.
Biostatistician - Research NemoursBiostatistician - ResearchWilmington, DERemoteFull timeThis includes, but is not limited to, assistance with designing clinical research studies, writing statistical sections of research proposals, calculating sample size and power, managing, analyzing and interpreting clinical data and databases, and authoring statistical analysis results for clinical study reports and manuscripts. Applicants must reside in one of the following states: Alabama, Colorado, Delaware, the District of Columbia, Florida, Georgia, Illinois, Maryland, Missouri, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Tennessee, Texas, and Virginia.
Principal Carelon Research Biostatistician Elevance Health IncPrincipal Carelon Research BiostatisticianWilmington, DE$136,000–$234,600 / yearThis researcher partners with investigators, research sponsors, academic institutions, and cross-functional project teams to design studies, develop statistical methodologies, oversee analytical execution, and communicate scientific findings that advance externally funded clinical research programs. Experience designing clinical research studies, developing sample size calculations, statistical analysis plans, outcome measures, and advanced statistical methodologies including survival analysis, causal inference, and experimental design preferred.
Research Technologist, Senior NemoursResearch Technologist, SeniorWilmington, 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 Senior Research Technologist leads, oversees, and independently sets up and performs experiments and procedures in support of laboratory goals and grant commitments (e.g., assays, cell/tissue culture, animal studies, equipment planning and ordering, etc.).
Pediatric Orthopedic Research Scholar - Pediatric Orthopedic Residency Program NemoursPediatric Orthopedic Research Scholar - Pediatric Orthopedic Residency ProgramWilmington, 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. We are seeking a physician who has completed all orthopaedic training and desires further post-graduate training in pediatric orthopaedics related research, for a one-year Pediatric Orthopedic Research Scholar position at Nemours Children's Health in Wilmington, DE.
Clinical Quality Program Manager Elevance HealthClinical Quality Program ManagerWilmington, DelawareWe 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. The Clinical Quality Program Manager is responsible for serving as a liaison with and overseeing the quality improvement activities/projects/programs for one or more states within a major line of business.
Intern-Research PHD NemoursIntern-Research PHDWilmington, 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. duPont Trust, our $1.7B nonprofit system is dedicated to improving children's health through clinical care, research, education, advocacy, and prevention.
Clinical Pharmacy Specialist (Hematology/Oncology, BBMT)) NemoursClinical Pharmacy Specialist (Hematology/Oncology, BBMT))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.
Clinical Affairs Specialist (M/F/D) (Limited To 15 Months) Getinge GroupClinical Affairs Specialist (M/F/D) (Limited To 15 Months)Rastatt, DEWith a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. Independently manage Investigator-Initiated Studies (IISs): review applications, evaluate proposals, presentation in IIS committee, draft contracts and negotiation and ensure successful execution through to study close-out.
Global Head of R&D & Clinical Development Sourcing Incyte CorporationGlobal Head of R&D & Clinical Development SourcingWilmington, DelawareThis 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.
Echocardiography Operational & Clinical Specialist, Cardiology NemoursEchocardiography Operational & Clinical Specialist, CardiologyWilmington, DEFull timeJefferson) relationships, supports interdepartmental relationships within Nemours, maintains the educational and CME structure of the lab, establishes and maintains a cadence of communication and process improvements with cardiology counterparts at Nemours-Florida, participates in procedural billing audits, and continuous improvement with other members of the operational teams (internal and external), and works hand in hand with the Epic and Enterprise Imaging Informatics teams to manage and optimize the technical components of the performance, transfer, and reporting of an Nemours and non-Nemours echocardiograms. Together, this team maintains ICAEL lab accreditation for all services provided, coordinates equipment purchasing and budgeting within each budget cycle, coordinates equipment maintenance and repair with biomed/vendors, supports growth and outreach initiatives throughout the Delaware Valley service area.
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.
Principal Investigator/Associate Director, Translational Biomarker Discovery Laboratory Incyte CorpPrincipal Investigator/Associate Director, Translational Biomarker Discovery LaboratoryWilmington, DEQualifications Minimal acceptable level of education work experience and competency • PhD or equivalent in Oncology Molecular Biology Systems Biology Immunology or a related life sciences discipline • 6-10 years of experience in translational research within pharma biotech or a comparable research environment • Strong demonstrable expertise in assay development optimization and implementation • Hands on experience with advanced molecular and cellular technologies and multi omic platforms • Proven ability to integrate biological data across multiple modalities to inform discovery and translational decisions • Experience working with human samples and clinically relevant model systems • Strong scientific communication skills and ability to collaborate effectively in matrixed teams Preferred • Experience supporting biomarker strategies for early clinical programs • Familiarity with oncology andor inflammatoryautoimmune disease biology • Experience interacting with toxicology DMB or CQP functions • Comfort working in a role that combines scientific independence with focused team oversight rather than large scale management Disclaimer The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. The Principal InvestigatorAssociate Director will primarily operate as a senior individual contributor with the potential to oversee a small team of laboratory scientists or matrixed contributors over time while remaining actively involved in experimental design assay execution and cross‑functional program support.
NewAssociate Computer Support Analyst Christiana Care Health SystemAssociate Computer Support AnalystDE$63,107.20–$100,984 / yearIncredible 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! Install, configure, test, maintain, monitor, and troubleshoot end user workstation hardware, telephony, mobile devices, clinical IT devices including nurse call, TV Systems, networked peripheral devices, and networking hardware products.
Associate Director, Market Access Strategy (Respiratory Biologics) AstraZeneca PlcAssociate Director, Market Access Strategy (Respiratory Biologics)Wilmington, DEPartners to recommend pricing and compliant payer contracting approaches aligned with brand P&L, including innovating approaches to evolving market challenges and contributing to the continuous improvement of market access strategies and execution. Partners with Brand teams to shape customer communication strategies and develop promotional assets that reflect access priorities and value messaging including pull through materials and negotiation frameworks.
Inbound/Outbound Queue Associate - Behavioral Health CVS Health CorpInbound/Outbound Queue Associate - Behavioral HealthDERemote$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.
NewAssociate 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, 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. The Translational Medicine (TLM) department of QPS is comprised of three laboratory operations units: Biomarker Analysis (BMA), Gene & Sequence Analysis (GSA), and Immunobioanalysis (IBA).
Associate Actuary Centene Corporation GroupAssociate ActuaryDERemote$87,700–$157,800 / yearCollaborating with cross-functional teams, including Medical Economics, Enterprise Partnerships, Network, and Clinical teams, to gather data, validate assumptions, and support ongoing initiatives. Additional responsibilities will include: Supporting the development and maintenance of financial models for Value-Based Care (VBC) contracts (e.g., assisting with shared savings/risk and capitation analyses in Excel).
Associate Actuary, Strategic Analytics Centene Corporation GroupAssociate Actuary, Strategic AnalyticsDERemote$87,700–$157,800 / yearStrategic 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.
Assistant or Associate Professor of Law, Delaware Law School Widener UniversityAssistant or Associate Professor of Law, Delaware Law SchoolDelawareRemoteThe large corporate community in Delaware and the varieties of legal practice opportunities in neighboring Pennsylvania, New Jersey, and Maryland offer students an unusually rich array of opportunities for experiential learning through internships and externships, a public interest law center, and numerous clinical programs. We are most in need of candidates interested in teaching Legal Methods/Research and Writing courses, complimented by teaching first year or other required or bar tested courses.
Implant 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.
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.
Program Coordinator (Bilingual) NemoursProgram Coordinator (Bilingual)Wilmington, DEFull timeAdditionally, the CRC will coordinate IRB submissions, recruiting study participants, obtaining informed consent, interacting with community-partners, youth, young adults and parents related to research projects, scheduling and conducting study procedures, collecting and recording study data, maintaining study records, assisting with coordinating financial contracts between community partners, participating in data collection and analysis, and the preparation of scientific presentations, manuscripts, reports, and grants. 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.
PSC Coordinator Brigham and Women's HospitalPSC CoordinatorDover, DE$19.81–$28.30 / hourThe framework is comprised of ten competencies (half People-Focused, half Performance-Focused) and are defined by observable and measurable skills and behaviors that contribute to workplace effectiveness and career success. At Mass General Brigham, our competency framework defines what effective leadership "looks like" by specifying which behaviors are most critical for successful performance at each job level.