NewClinical Research Coordinator JouléClinical Research CoordinatorWest Chester, PA$26–$30 / hourProficiency with electronic data capture systems, clinical trial management software, and Microsoft Office (Excel, Word, and PowerPoint) preferred. System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America.
Clinical Specialist JouléClinical SpecialistExton, PAThe ideal candidate will be the go-to expert for device training, therapy education, and enrollment support, ensuring that the trials are conducted with the highest level of clinical integrity. We are looking for a seasoned Registered Respiratory Therapist (RRT) with a strong background in clinical research to join our client's team in a high-impact, mobile role.
NewRespiratory Account Manager JouléRespiratory Account ManagerExton, PARemoteSystem One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. This role involves traveling within the southeastern US and working closely with healthcare professionals to drive treatment outcomes.
Laboratory Manager, Clinical Safety Laboratory QPS Holdings LLCLaboratory Manager, Clinical Safety LaboratoryNewark, DEThe Laboratory Manager will play a key role in the continued development and expansion of the Clinical Safety Laboratory in Groningen, helping shape laboratory operations, workflows, and team capabilities as the lab continues to grow. This opportunity is ideal for an experienced laboratory professional with a hands-on mentality who enjoys building and improving processes while also leading the day-to-day operations within a highly flexible and complex Clinical Safety Laboratory environment.
Clinical Research Coord II Main Line Health SystemClinical Research Coord IIWynnewood, PA$50,793.60–$78,707.20 / yearDaily tasks are conducted on site at the Main Line Health Hospitals and may include the oversight and coordination of a variety of clinical studies, executing study procedures as outlined by the study protocol (and related documents). Just as each of our patients requires a personalized care plan, each of our employees, physicians, and volunteers, bring distinctive talents to Main Line Health.
Clinical Trials Manager NemoursClinical Trials ManagerWilmington, 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. Collaborating with Research partners across multiple Nemours sites and Non-Nemours sites this leadership role will work in conjunction with the enterprise coalition for the Nemours Center for Cancer and Blood Disorders (NCCBD).
NewClinical Research Coordinator Integrated Resources, IncClinical Research CoordinatorMalvern, PennsylvaniaFull timeClient provides medicines for an array of health concerns in several therapeutic areas, including: attention deficit hyperactivity disorder (ADHD), cardiovascular disease, general medicine (acid reflux disease, infectious diseases), mental health (bipolar I disorder, schizophrenia), neurologics (Alzheimer's disease, epilepsy, migraine prevention and treatment), pain management, and women's health. The Temperature Management Coordinator is responsible for day to day the execution management of the Temperature Management & Control for Clinical Supplies clinical supplies during the execution phase of clinical trials consistent with GMP guidelines with a specific focus on Temperature Management & Control of Clinical Supplies.
Clinical Research Technologist II NemoursClinical Research Technologist IIWilmington, 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 Clinical Research Technologist II serves as a bench technologist for the laboratories in the research department performing CAP and/or CLIA licensed clinical diagnostic tests and other regulatory accredited activities such as biorepositories.
Clinical Research Coordinator II- Orthopedics NemoursClinical Research Coordinator II- OrthopedicsWilmington, DEFull timeThe 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.
Senior Clinical Research Associate Alexion Pharmaceuticals IncSenior Clinical Research AssociateWilmington, DECRA works in close collaboration with (Project Management Clinical Operations (PMCO), Study Start-Up (SSU) manager, Clinical Study Assistant (CSA) and other CRAs in Country Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner in the country level. CRA is responsible for the selection, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with Alexion Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.
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.
NewClinical Trial Assistant Integrated Resources, IncClinical Trial AssistantMalvern, PennsylvaniaContractorDescription of the Role•Responsible for management of all temperature excursions associated to clinical supplies during the trial execution ensuring prompt resolution and compliance with all SOP, GMP, Quality, and Regulatory guidelines, contributing to successful subject dosing within Pharma R&D for all phases of clinical trials•Act as a single point of contact accountable for the business critical need•Manage and adjust supply dispositions via inventory systems including IVR & IWR•Conduct issue resolution activities for the temperature excursion supply aspects of the clinical trials•Develop strong internal collaboration with GCO, DPD, and Quality stakeholders to ensure TOR resolution and overall customer satisfaction•Interface with Global Trial Managers, Trial Supply Managers, Drug Product Development, and Quality to manage trial supply temperature excursions•Responsible for execution of Temperature Monitoring Coordinator role during trial feasibility and throughout trial execution driving robust temperature management within Pharma R&D for all phases of clinical trials•Review and approval of all Investigational Site Temperature Management Equipment Questionnaire Approvals (TMEQ) for Cold Chain IMP•Act as subject matter experts for temperature management requirements including storage and monitoring capabilities•Customizing protocol specific temperature out-of-range forms based on product attributes•Coordinating quote request and PO setup process to centrally source temperature monitoring devices•Develop strong internal collaboration with GCO stakeholders to ensure customer satisfaction•Partner with Global Trial Managers, Local Trial Managers, Site Managers, Local Medication Coordinators, Clinical Supplies Design Leaders, and Central Business Operations in temperature management and issue resolution•Supports business process improvement initiatives. inventory management functionality)•Experience with the following functions preferred: clinical operations, logistics, quality assurance, clinical supply chain planning, drug product development•Demonstrated knowledge in the following areas:•Clinical Supply Distribution•Clinical Study Execution/GCP•Intermediate to advanced software skills (e.g., Microsoft Excel, SharePoint, PowerPoint)•Experience in a highly matrixed environment (preferred)Critical Competencies:•Very strong data analysis and problem solving experience•Highly organized with strong attention to detail•Extreme sense of urgency for the tasks at hand, including ability to drive resolution with minimal management oversight•Excellent written and verbal communication skills•Task oriented (repetitive process)•Strong quality management skills•Strong strategic thinking skills•Excellent problem solving and decision making skills•Strong cross-functional coordination skillsAdditional InformationFeel free to forward my email to your friends/colleagues who might be available.
NewClinical Dictionary Analyst Integrated Resources, IncClinical Dictionary AnalystMalvern, PennsylvaniaFull timeUndertake coding and review of verbatim terms when necessary to successfully meet project timelinesEnsure coders adhere to establish processes/proceduresCommunicate progress and issues related to coding assignments to Head, Dictionary Group and DML/CDM (as appropriate)Assist in identifying and implementing new dictionaries and software improvements (ds Navigator, eDM, etc.)Assist in development and maintenance of Dictionary SOPs and Working InstructionsAssist Coders in writing and resolving dictionary queriesUndertake sample based Q.C. of synonym additions. Clinical Dictionary Analyst - The Global Dictionary Analyst is responsible for facilitating Dictionary management processes, including maintaining and supporting the development of clinical dictionaries used in clinical data analysis.
NewClinical Dictionary Analystma Integrated Resources, IncClinical Dictionary AnalystmaMalvern, PennsylvaniaContractorUndertake coding and review of verbatim terms when necessary to successfully meet project timelinesEnsure coders adhere to establish processes/proceduresCommunicate progress and issues related to coding assignments to Head, Dictionary Group and DML/CDM (as appropriate)Assist in identifying and implementing new dictionaries and software improvements (ds Navigator, eDM, etc.)Assist in development and maintenance of Dictionary SOPs and Working InstructionsAssist Coders in writing and resolving dictionary queriesUndertake sample based Q.C. of synonym additions. Job DescriptionClinical Dictionary Analyst - The Global Dictionary Analyst is responsible for facilitating Dictionary management processes, including maintaining and supporting the development of clinical dictionaries used in clinical data analysis.
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.
Senior Director Clinical Research Scientist Incyte CorporationSenior Director Clinical Research ScientistWilmington, DelawareContribute to the development of program strategy for assigned compounds/programs including participation in the preparation of clinical development plans Drafting and review of clinical scientific documents such as IND, 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, Incyte’s data protection officer, and your supervisory authority (if applicable).
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.
Data Analytics Manager (Clinical) Incyte CorpData Analytics Manager (Clinical)Chadds Ford, PAThrough 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. 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.
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.
NewClinical Data Managers/Analyst Integrated Resources, IncClinical Data Managers/AnalystMalvern, PennsylvaniaContractorClinical Data Managers/AnalystA Few Words About Us Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. Looking for Clinical Data Managers/Analyst in Malvern, PAClient -Johnson and JohnsonPlease share the updated resume at sweta(at)irionline.com
Clinical Manager Nursing Support Services Penn MedicineClinical Manager Nursing Support ServicesWest Chester, PAPenn Medicine is dedicated to our tripartite mission of providing the highest level of care to patients, conducting innovative research, and educating future leaders in the field of medicine. Responsible for Management and Nursing Leadership of Nursing Office (Staffing Coordinator, Nursing Supervisors and Med-Surg/Tele Select Float Pool (SFP).
RN Clinical Care Manager in West Chester Penn MedicineRN Clinical Care Manager in West ChesterWest Chester, PATriages patient telephone calls and provides consultation regarding ongoing symptom management resulting from treatment and disease, analysis of intervention regarding diagnostic work-up, assessing and managing acute emergencies, managing family concerns as needed, liaison activities with affiliated physicians, nurses, pharmacists and emergency rooms. Creates, uses, and maintains patient-specific care management tracking system that identifies/ reports on patients who will benefit from care management services, the subsequent patient progress, and associated interventions.
NewClinical Research Coordinator RN Registered Nurse (Full Time/Days) Penn MedicineClinical Research Coordinator RN Registered Nurse (Full Time/Days)Lancaster, PAQualified individuals must have the ability with or without reasonable accommodation to perform the following duties: Plans and coordinates assigned research studies, serves as principle liaison for the project, interfaces with research subjects and collects research data, oversees administrative support, develops appropriate tools needed to conduct the research, and maintains record keeping systems and procedures. Position Summary: Plans, initiates, coordinates, implements, and oversees clinical trials within the LGHealth Research Institute under the direction of the clinical Principal Investigator PI who is responsible for the overall conduct and management of the clinical trial.
Clinical Sales Specialist, Electrophysiology - LAAO (Philadelphia/Wilmington) Abbott LaboratoriesClinical Sales Specialist, Electrophysiology - LAAO (Philadelphia/Wilmington)Wilmington, DE$61,300–$122,700 / yearIn this role, the Clinical Specialist with train interventional cardiologists, catheter lab staff and ancillary personnel on the use of Structural Heart products and provide technical support to physicians during procedures. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.
Executive Director, Oncology Translational Medicine, Clinical Pharmacology Modeling And Simulation GSK, Plc.Executive Director, Oncology Translational Medicine, Clinical Pharmacology Modeling And SimulationUpper Providence, PAinput on development of efficient and effective modeling and simulation strategies, including population PK, exposure-response analysis, and physiologically based PK (PBPK) to support clinical trial design, justification of dosing regimen, and provide supportive evidence of efficacy and safety for regulatory submissions. Animal Models, Artificial Intelligence (AI), Clinical Pharmacology, Drug Design, Drug Discovery Process, Drug Discovery Research, In Vitro Models, Medication Safety, Molecular Modeling, Oncology, Pharmacodynamics, Pharmacokinetics, Pharmacometrics, Pharmacovigilance, Target Validation.
Manager, Clinical Data Management Immunocore Holdings PlcManager, Clinical Data ManagementRadnor, PA$107,250–$178,750 / yearVacancy NameManager, Clinical Data Management Vacancy NoVN822 Employment TypeFull Time Location of roleRadnor, PA DepartmentClinical Operations Key ResponsibilitiesThe Manager Clinical Data Management will be responsible for performing/overseeing outsourced (and in-house) Data Management activities as the Lead Clinical Data Manager, to support Immunocore clinical trials worldwide. US Salary Range: $107,250 to $178,750 About the CompanyImmunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseases and autoimmune disease.
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.
Sr Global Product Manager, MCT Clinical Systems PhilipsSr Global Product Manager, MCT Clinical SystemsMalvern, PA$130,000–$209,000 / yearAs our Senior Product Manager within Philips Ambulatory & Monitoring Diagnostics (AM&D) Service Solutions team, you will collaborate in defining the Mobile Cardiac Telemetry (MCT) clinical systems product strategy for that aligns to the AM&D portfolio vision and global market alignment. The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.
Sr Global Product Manager, Clinical Systems PhilipsSr Global Product Manager, Clinical SystemsMalvern, PA$130,000–$209,000 / yearAs our Senior Product Manager within Philips Ambulatory & Monitoring Diagnostics (AM&D) Service Solutions team, you will collaborate in defining the clinical systems product strategy that aligns to the AM&D portfolio vision and global market alignment. The actual base pay offered may vary within the posted ranges depending on multiple factors including job-related knowledge/skills, experience, business needs, geographical location, and internal equity.
Senior Manager, Clinical Data Standards Immunocore Holdings PlcSenior Manager, Clinical Data StandardsRadnor, PA$121,500–$202,500 / year121,500-$202,500 About the CompanyImmunocore (NASDAQ: IMCR) is a pioneering, commercial-stage T cell receptor biotechnology company whose purpose is to develop and commercialize a new generation of transformative medicines which address unmet patient needs in oncology, infectious diseases and autoimmune disease. Our ImmTAX molecules underpin a new generation of precision engineered drugs that harness the immune system to treat a broad spectrum of diseases with high unmet medical need, including oncology, infectious diseases and autoimmune diseases.
NewRN Clinical Manager Strong Force StaffingRN Clinical ManagerElkton, MarylandJoin our clients compassionate team in Elkton, MD, as a Certified Nursing Assistant (CNA) for hospice care. We are eager to facilitate your application and help you land a fulfilling leadership role with our clients compassionate team.
NewSenior Program Manager – Veeva Vault Clinical (Life Sciences R&D) IconmaSenior Program Manager – Veeva Vault Clinical (Life Sciences R&D)Wilmington, DELife Sciences R&D GxP experienced Global Program Manager (for client’s program scope) with experience in successfully program managing a Veeva Vault Clinical (CTMS, Site Connect preferred else eTMF) implementation. Our Client, an IT Services and Consultant company, is looking for a Senior Program Manager – Veeva Vault Clinical (Life Sciences R&D) for their Wilmington, DE/ Hybrid location.
Senior Manager, Clinical Supply Chain Program Lead Immunocore Holdings PlcSenior Manager, Clinical Supply Chain Program LeadRadnor, PARegulatory Sciences Clinical Sciences Commercial as necessary • Monitors and is responsible for communicating the spend versus budget for clinical supply program activities and materials leads Clinical Supply Chain and Finance review meetings and flags variances • Reviews changes to contracts with vendors and Contracts Manager if necessary • May manage the procurement of IMP and ancillary materials as it relates to programs • Manages and reviews inventory levels at manufacturing facilities to ensure supplies are adequate according to the demand • Provides support to ensure compliance with internal Quality Management system including writing and reviewing SOPs • When required contributes to and reviews documents for submissions to regulators or ethics committees • Contributes to and reviews supply and technical agreements ensuring Quality oversight • Initiates Quality Events where appropriate and investigate and perform root cause analysis and execution of associated CAPAs • May deputize for the Senior Director Clinical Supply Chain when absent as required • Supports the selection of suppliers and assist with the preparation of documentation associated with the assessment evaluation and management of CMOs distribution depots and other contractors involved with clinical supplies • Drives forward procedural change to improve compliance with SOPs regulations. KEY RESPONSIBILITIES • Sets up the clinical supply chain strategy and strategic direction of supply for clinical programs • Leads Clinical Supply Chain Managers Specialists responsible for the production packaging labelling and distribution of drug supplies for clinical studies providing direction around study supply strategies ensuring plans are appropriately aligned with business needs • Ensures the supply chain strategy maximizes efficiency of supply consistently balancing cost and risk • Aggregates the demand for Clinical program supply and ensures it is included in the Immunocore CMC and External Manufacturing supply planning process • Produces and implements a Clinical Supply Chain Program Strategy document documenting the supply chain program strategy • Implements continuous improvement aimed at scalability and applicability across programs • Supports requests for supply for external sponsor studies compassionate use and access programs collaborating with and seeking expert input from cross functional subject matter experts e.g.
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 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. Locations: This role requires associates to be in-office 1-2 days per week, fostering collaboration and connectivity, while providing flexibility to support productivity and work-life balance.
NewEchocardiography 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.
Clinical Director Behavior Analyst BCBA Success On The SpectrumClinical Director Behavior Analyst BCBALancaster, Pennsylvania$105,000–$115,000Quarterly, you will analyze the progress of clients company-wide and lead in-service trainings based on your staffs’ weaknesses. We also encourage high parent involvement and allow parents to watch their child’s therapy live from our viewing room!
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.
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.
Clinical Services Supervisor Penn MedicineClinical Services SupervisorRadnor, PASummary: The Clinical Services Supervisor will be responsible for supporting the day-to-day operational needs of the outpatient practice including staffing coverage, office and medical supply inventory management, physician room assignments, and provider schedules. The Clinical Services Supervisor will provide direct oversight to the ancillary staff and support planned and unplanned vacancies to ensure optimal workflow is preserved in the clinic.
Clinical Services Associate Penn MedicineClinical Services AssociateExton, PAAccountabilities: Patient Care Accountabilities: Promptly rooms patients, using EMR to alert provider that patient is ready: reviews past medical, surgical, family, smoking history, allergies, medications; notes corrections in EMR, notes medication refills needed for the physician to review, initiates self-management goal setting where appropriate, obtains patient's vital signs and documents in EMR, prepares chart for patient visit, understands insurance restrictions for lab work, referral needs, precertification requirements, etc. Specimen management: obtain specimens for testing if applicable (including performing phlebotomy and anterior nares nasal swab collections), performs laboratory and screening tests, records results in EMR and reconciles with logs where appropriate, documents and reports findings to providers, performs all quality controls as per Point of Care Testing guidelines, prepares specimens for transport as necessary.
Clinical Services Associate - Cancer Center VF Penn MedicineClinical Services Associate - Cancer Center VFPAResponsibilities: Patient Care Accountabilities: Promptly rooms patients, using EMR to alert provider that patient is ready: reviews past medical, surgical, family, smoking history, allergies, medications; notes corrections in EMR, notes medication refills needed for the physician to review, initiates self-management goal setting where appropriate, obtains patient's vital signs and documents in EMR, prepares chart for patient visit, understands insurance restrictions for lab work, referral needs, precertification requirements, etc. Specimen management: obtain specimens for testing if applicable (including performing phlebotomy and anterior nares nasal swab collections), performs laboratory and screening tests, records results in EMR and reconciles with logs where appropriate, documents and reports findings to providers, performs all quality controls as per Point of Care Testing guidelines, prepares specimens for transport as necessary.
Clinical Account Manager - Southeast Pennsylvania Ceribell, IncClinical Account Manager - Southeast PennsylvaniaLancaster, PA$100,000–$180,000 / yearThe Ceribell System is a novel, point-of-care electroencephalography ("EEG") platform specifically designed to address the unmet needs of patients in the acute care setting, and is being used in hundreds of community hospitals, large academic facilities and major IDN's across the country. 3-5 years of recent critical care sales experience OR 5 years of medical device or pharma sales experience OR RN's with industry experience in supporting sales teams.
Clinical Sales Manager Intuitive Surgical IncClinical Sales ManagerWilmington, DEU.S. Export Controls Disclaimer: In accordance with the U.S. Export Administration Regulations (15 CFR §743.13(b)), some roles at Intuitive Surgical may be subject to U.S. export controls for prospective employees who are nationals from countries currently on embargo or sanctions status. Certain information you provide as part of the application will be used for purposes of determining whether Intuitive Surgical will need to (i) obtain an export license from the U.S. Government on your behalf (note: the government's licensing process can take 3 to 6+ months) or (ii) implement a Technology Control Plan ("TCP") (note: typically adds 2 weeks to the hiring process).
Clinical Services Coordinator Penn Medicine Radnor Penn MedicineClinical Services Coordinator Penn Medicine RadnorRadnor, PAMedical Assistant Accountabilities: Promptly rooms patients, using EMR to alert provider that patient is ready: reviews past medical, surgical, family, smoking history, allergies, medications; notes corrections in EMR, notes medication refills needed for the physician to review, initiates self-management goal setting where appropriate, obtains patient's vital signs and documents in EMR, prepares chart for patient visit, understands insurance restrictions for lab work, referral needs, precertification requirements, etc. Specimen management: obtain specimens for testing if applicable, performs laboratory and screening tests, records results in EMR and reconciles with logs where appropriate, documents and reports findings to providers, performs all quality controls as per Point of Care Testing guidelines, prepares specimens for transport as necessary.
Executive Director, Clinical Development - Hematology Oncology Incyte CorpExecutive Director, Clinical Development - Hematology OncologyWilmington, DEWe are looking for a Senior Director Oncology Drug Development to lead the design and execution of clinical development strategies for oncology programs across Phase I-III for Incytes oncology products. Oversees the development of key clinical and scientific documents including protocols informed consent forms clinical study reports CSRs investigator materials regulatory documents publications and development plans.
Ophthalmic Technician II - Ophth Clinical Support Radnor Penn MedicineOphthalmic Technician II - Ophth Clinical Support RadnorRadnor, PACompletes preliminary ocular exam including visual acuities, color vision, lensometry, cover tests, motility tests, stereopsis tests, external examination, pupil evaluation, slit lamp biomicroscopy, intraocular pressures, refractometry,, pachymetry, vital signs, Administer eye medications according to protocol. The Ophthalmic Technician is accountable for the provision of direct care to patients, who range in age from infancy to the elderly, and demonstrates care within the competency domains of Continuous Quality Improvement, Person and family centered care, Professionalism, Safety, Teamwork, and Technology.
Clinical Practice Leader ICU Penn MedicineClinical Practice Leader ICUWest Chester, PAA strong CPL must be able to: (a) communicate effectively toward negotiating multiple perspectives within the organization and driving change; (b) demonstrate clinical judgment and establish clinical credibility with nursing and interprofessional colleagues within his/her specialty area; (c) exhibit self-direction in maintaining professional knowledge and competence within his/her specialty area; (d) apply critical thinking and analytic skills to design and implement change initiatives; (e) build rapport with and provide mentorship to clinical nurses; and (f) partner effectively with nurse manager colleagues to advance professional nursing practice. Leveraging advanced education and training, CPLs are accountable for leading nursing practice by supporting nurses to care for patients at the bedside, driving practice changes at the unit, service line, and systems levels, and ensuring the use of best practices and evidence-based care to achieve the best possible patient outcomes.
Clinical Cosmetologist Penn MedicineClinical CosmetologistLancaster, PAAnswers telephone, relays messages, screens calls, schedules patient appointments, and greets and directs patients, salespeople, and visitors. Penn Medicine is dedicated to our tripartite mission of providing the highest level of care to patients, conducting innovative research, and educating future leaders in the field of medicine.
NewLicensed Clinical Manager | SUD and Mental Health Kolmac Integrated Behavioral HealthLicensed Clinical Manager | SUD and Mental HealthNorth East, MD$70,000–$85,000 / yearThis is a high-impact leadership role for someone who wants to shape clinical quality, develop counselors, and directly influence patient outcomes — with real authority to make it happen. As Clinical Manager, you'll own the daily administration and clinical quality of CCG's services, partnering closely with the Executive Director to drive both team performance and patient outcomes.