NewStaff - Registered Nurse (RN) - Clinical Liaison - $72K-98K per year GentivaStaff - Registered Nurse (RN) - Clinical Liaison - $72K-98K per yearChadds Ford, PA$72,000–$98,000 / yearWith more than 550 locations and thousands of compassionate clinicians across 38 states, our place is by the side of those who need us – from helping people recover from illness, injury, or surgery in the comfort of their homes to guiding patients and their families through the physical, emotional, and spiritual effects of a serious illness or terminal diagnosis. Our nationwide reach is powered by a family of trusted brands that include: Hospice care: Gentiva Hospice, Emerald Coast Hospice Care, Heartland Hospice, Hospice Plus, New Century Hospice, Regency SouthernCare, SouthernCare Hospice Services, SouthernCare New Beacon.
NewClinical 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.
NewRegistered Nurse (RN) - Clinical Liaison - $72K-98K per year GentivaRegistered Nurse (RN) - Clinical Liaison - $72K-98K per yearThornton, PA$72,000–$98,000 / yearWith more than 550 locations and thousands of compassionate clinicians across 38 states, our place is by the side of those who need us – from helping people recover from illness, injury, or surgery in the comfort of their homes to guiding patients and their families through the physical, emotional, and spiritual effects of a serious illness or terminal diagnosis. Our nationwide reach is powered by a family of trusted brands that include: Hospice care: Gentiva Hospice, Emerald Coast Hospice Care, Heartland Hospice, Hospice Plus, New Century Hospice, Regency SouthernCare, SouthernCare Hospice Services, SouthernCare New Beacon.
NewClinical Research Assistant I - Division of Emergency Medicine Part Time Children's Hospital of PhiladelphiaClinical Research Assistant I - Division of Emergency Medicine Part TimeKing of Prussia, PA$21.05–$26.35 / hourUnder the supervision of the Program Manager and the Associate Director of Research Operations, the research assistant responsibilities include coordinating clinical research activities within the scope of specific research protocols under the guidance of the study PI and Program Manager. The Division of Emergency Medicine (DoEM) is seeking a part-time clinical research assistant who will join a highly productive research team focused on conducting a variety of research projects at our King of Prussia location.
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 Director, Clinical Research, Hematology Merck & Co IncClinical Director, Clinical Research, HematologyPA$255,800–$402,700 / yearThe Clinical Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies. The Clinical Director (Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area, specifically in our Hematology Section.
Senior Clinical Director, Clinical Research, Hematology Merck & Co IncSenior Clinical Director, Clinical Research, HematologyPA$282,200–$444,200 / yearThe Senior Clinical Director (Senior Principal Scientist) has primary responsibility for planning and directing clinical research activities involving new or marketed medicines in the Oncology therapeutic area, specifically in our Hematology Section. The Senior Director is responsible for maintaining a strong scientific fund of knowledge by: Maintaining awareness of scientific developments within his/her area of expertise, in terms of new scientific findings, research methodologies.
NewClinical 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.
NewClinical Scientist Integrated Resources, IncClinical ScientistCollegeville, PennsylvaniaContractorD. Degree in science or health-related field preferred, will consider highly motivated and experienced MA or MS• 10+ years of pharmaceutical/CRO experience preferredTECHNICAL SKILLS:• Has extensive knowledge of the clinical research process and Good Clinical Practices from previous employment experience in the clinical research field• Has demonstrated ability and level of experience with integrating and summarizing medical/scientific concepts in protocols and other clinical documents• Has independently authored clinical study documents• Has experience with participating in and informally leading an operational team• Applies knowledge of internal/external business challenges to facilitate process improvements• Has ability to proactively resolve issues and work independently with minimal supervision• Has working knowledge of statistics, data analysis, and data interpretation• Has exceptional written and oral communication and cross-functional collaborative skills• Is proficient in MS Word, Excel, and PowerPointJob LocationI'm interested Clinical ScientistA 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.
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.
Executive Director, Product Development Team Leader, Clinical Research, Hematology - Lymphoma Merck & Co IncExecutive Director, Product Development Team Leader, Clinical Research, Hematology - LymphomaPA$310,900–$489,400 / yearWorking closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects, and assist the Associate Vice President and/or Vice President in ensuring that appropriate Corporate personnel are informed of the progress of studies of our company and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to their areas of responsibility. Leading internal governance presentations to senior management and committees, communicating progress and key changes in product development strategy between stage gates, ensuring early alignment with line management, and facilitating issue escalation and cross-functional collaboration as needed for governance approval.
NewClinical Outsourcing Lead Integrated Resources, IncClinical Outsourcing LeadCollegeville, PennsylvaniaFull timeJob DescriptionTechnical Skill RequirementsFinance / clinical budgetingDemonstrates clear understanding of activity based costs along study path; additionally, Director Level (P05) demonstrates expertise in strategic cost relationships and links (program, asset, portfolio, etc.) for planning and forecasting, negotiation, and higher level presentationUnderstands components of clinical & per subject costing & use of industry benchmarkingOperational expertise in study scheduling and placementKnowledge of clinical study outsourcing; Director Level (P05) requires expert knowledge in clinical trial development outsourcingUnderstanding of operational impact to timelines, budget, and quality desired, and required for Director Level (P05)Negotiating and contracting skillsKnowledge and experience of contracting with external service providersApplication of contracting strategies at enterprise levelsInternal and external influencing abilities for expectation and timeline management; for Director Level (P05), proven experience requiredIdentifies and leads efforts to examine multiple solutions or innovative options in solving highly complex problems directly impacting a Global Business Unit/Global Operating Unit or Sub Business Unit/Sub Operating UnitQualificationsQualificationsBA or BS degree and/or recognized amount of work experience (preferably in a related discipline).An advanced degree (MBA, JD, etc.), prior management responsibilities, and/or substantial work experience is preferential for the Director Level (P05).Clinical trials Sponsor experience, CRO operational and/or BD experience, or other trial related experience, including significant experience negotiating and drafting clinical trial-related agreements is required. Excellent oral/written communication skills and proficiency with MS Office applications (Word/PPT/Excel) required: experience with ACW, ClearTrial, Grants Manager and / or other industry cost and planning tools preferred.
Senior Scientist, Clinical Research Merck & Co IncSenior Scientist, Clinical ResearchWest Point, PA$117,000–$184,200 / yearCo-authors clinical sections of protocols, clinical investigator brochures, clinical study reports, Worldwide Marketing Application/Common Technical Document (WMA/CTD) subsections, and regulatory agency update and safety reports, as well as clinical development plans, publications, and abstracts. Experience managing Immunology and/or vaccine trials with an ability to think outside of the box, explore novel ways of working and comfortably navigate ambiguity to drive results also a plus.
Associate Business Development Director - Clinical Technology Sales IQVIAAssociate Business Development Director - Clinical Technology SalesWayne, PennsylvaniaThis role focuses on business creation, account expansion, and strategic customer engagement, partnering closely with IQVIA clinical, operational, and technical teams to deliver technology‑enabled solutions for complex clinical trials. Build and maintain strong, long‑term relationships with key sponsor decisionmakers and influencers, developing a deep understanding of customer organizations, business needs, study pipelines, and technology strategies.
Associate Principal Biostatistician Clinical Safety Statistics (CSS) Merck & Co IncAssociate Principal Biostatistician Clinical Safety Statistics (CSS)North Wales, PA$142,400–$224,100 / yearIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. Required Skills: Clinical Development, Clinical Research, Clinical Safety, Clinical Study Design, Drug Development, Preclinical Research, Regulatory Compliance, Regulatory Documents, Regulatory Requirements, Safety Databases, Safety Evaluation, Scientific Modeling, Statistical Graphics, Statistical Research, Statistics, Vaccine Safety, Visual Analytics.
Principal Scientist, Clinical Research - Immunology/Dermatology Merck & Co IncPrincipal Scientist, Clinical Research - Immunology/DermatologyNorth Wales, PA$255,800–$402,700 / yearAssist the Senior Director, Associate Vice-President/Vice-President and Product Development Team Lead in ensuring that appropriate corporate personnel is informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific questions relevant to their areas of responsibility. With a focus on late-stage development, the Clinical Director will manage the entire cycle of clinical development, including determination of appropriate disease indications to pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication.
NewSenior 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.
Account Manager (Clinical Outcomes Assessments) - Mapi Research Trust ICON PlcAccount Manager (Clinical Outcomes Assessments) - Mapi Research TrustBlue Bell, PARemoteWe promote scientific approaches in the PCO field and encourages exchanges between academics, pharmaceutical companies, and international organizations around the world in the service of incorporating the patient's voice into every step of the development process of new treatments. Mapi Research Trust is a non-profit organization facilitating access to information for all stakeholders in the field of Patient Centered Outcomes, particularly for Clinical Outcome Assessments (COAs).
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.
Clinical Research Coordinator NemoursClinical Research CoordinatorWilmington, DEFull timeNemours is seeking a Clinical Research Coordinator to join our Nemours Children's Health team in Wilmington, DE.The Clinical Research Coordinator coordinates, implements and completes clinical research studies and/or clinical trials in the Orthogenetics Department at Nemours Children's Hospital Delaware by assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent/consent forms, educating parents/participants, scheduling and conducting study procedures, collecting and recording study data, maintaining detailed study records, interfacing with study sponsors, participation in sponsor study monitoring visits, prepare for and participate in internal and external research audits, maintain various research databases. We deliver care across six states through two freestanding children's hospitals - Nemours Children's Hospital, Delaware and Nemours Children's Hospital, Florida - along with a network of more than 80 primary, urgent, and specialty care practices and more than 40 hospital partnerships.
Senior Clinical Trial Manager ICON PlcSenior Clinical Trial ManagerBlue Bell, PAAs a Senior Clinical Trial Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programs. What You Will Do: Your focus will be on coordinating clinical trial management delivery, resolving issues, and developing team capability.
Scientific AVP, Clinical Research, Oncology Early Development Merck & Co IncScientific AVP, Clinical Research, Oncology Early DevelopmentPA$342,800–$539,600 / yearExternal outreach and leadership: Stays abreast of professional information, industry trends, and emerging technology through conferences, medical literature, and other available training, to augment expertise in drug development and the pharmaceutical industry. The successful candidate will collaborate and partner with cross-functional subject matter experts across our company and site footprint and be accountable for advancement of programs from candidate stage to clinical proof of concept milestones.
Manager, Clinical Vendor Mgmt 1 ICON PlcManager, Clinical Vendor Mgmt 1Blue Bell, PARequired qualifications and experience: Bachelor's degree in business, supply chain management, or a related field is preferred, with extensive experience in procurement or supply chain management. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Site Manager II ICON PlcClinical Site Manager IIBlue Bell, TXICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Clinical Research Nurse II/Sonographer ICON PlcClinical Research Nurse II/SonographerBlue Bell, WAICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
NewSenior Clinical Research Associate ICON PlcSenior Clinical Research AssociateBlue Bell, PARemoteAs a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.
Clinical Data Coordinator Madrigal Pharmaceuticals IncClinical Data CoordinatorConshohocken, PA$73,200–$89,500 / yearPlease know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process. Madrigal is a biopharmaceutical company focused on delivering novel therapeutics for metabolic dysfunction-associated steatohepatitis (MASH), a serious liver disease that can progress to cirrhosis, liver failure, need for liver transplantation and premature mortality.
Senior Principal Scientist, Clinical Research, Breast Cancer Merck & Co IncSenior Principal Scientist, Clinical Research, Breast CancerNorth Wales, PA$282,200–$444,200 / yearMonitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed Oncology drugs; Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and. Assist the Senior/Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our Company's and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.
Prin. Scientist, Clinical Research Merck & Co IncPrin. Scientist, Clinical ResearchWest Point, PA$190,800–$300,300 / yearInterface broadly with key functions including Discovery Sciences, Preclinical Pharmacology, Pharmaceutical Sciences, Toxicology, Translational Biomarkers, Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs, and late-stage Clinical Research throughout research sites around the world. Contributing to the identification of novel targets by partnering with discovery research teams to bring a clinical perspective into the earliest stages of target identification and validation, and executing clinical studies to evaluate the relevance of potential targets to human disease in order to justify investment in clinical development programs.
Senior Manager, Clinical Operations ICON PlcSenior Manager, Clinical OperationsBlue Bell, PARequired qualifications and experience: Bachelor's degree in project management, business, or a related field is preferred, with significant experience in project management and team leadership. Key responsibilities include: Developing and managing detailed project plans, including timelines, budgets, and resource allocation to ensure successful project delivery.
Clinical Research Nurse II/Mid-Wife ICON PlcClinical Research Nurse II/Mid-WifeBlue Bell, WAMinimum of 2-3 years of clinical nursing experience, preferably in a research or academic healthcare setting, with demonstrated knowledge of clinical trial operations, GCP guidelines, and regulatory requirements governing human subjects research. Proficiency in electronic medical record (EMR) systems, data management tools, and Microsoft Office applications, with a high level of attention to detail and accuracy in documenting patient information and study data.
Senior Principal Scientist, Clinical Research, Immunology Merck & Co IncSenior Principal Scientist, Clinical Research, ImmunologyNorth Wales, PA$282,200–$444,200 / yearWork closely with a cross-functional group of experts in commercialization, regulatory affairs, statistics, and manufacturing to manage clinical development projects; and assist the Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. Required Skills: Clinical Development, Clinical Medicine, Clinical Research Management, Clinical Studies, Clinical Trial Development, Clinical Trials, Dermatology, Drug Development, Gastroenterology, Inflammatory Bowel Diseases, Pharmaceutical Industry, Regulatory Compliance, Rheumatology.
Senior Medical Director, Clinical Development - Neurodegeneration GSK plcSenior Medical Director, Clinical Development - NeurodegenerationCollegeville, PA$284,625–$474,375 / yearGSK is seeking a highly skilled Senior Medical Director, Clinical Development, Neurodegeneration to provide clinical and scientific leadership for potential new, established and emerging indications for assets in clinical development with a strong focus on neurodegenerative disease including Alzheimer's Dementia (AD). Key Responsibilities: Lead the clinical development strategy from a drug or program including accountability for the clinical components of the Target Medicine Profile (TMP) and leadership of the clinical matrix team (CMT).
Clinical Research Associate ICON PlcClinical Research AssociateBlue Bell, PAAs a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Minimum of 9 months onsite monitoring experience as a Clinical Research Associate; level (CRA I, CRA II, or Senior CRA) determined by total years of experience.
Clinical Trial Associate Avalo TherapeuticsClinical Trial AssociateChesterbrook, PAAny resumes submitted without an agreement and/or any resumes sent unsolicited through e-mail accounts of Avalo employees will be considered outside of the appropriate process, do not imply or create any obligation on our part, do not impart any restrictions on Avalo with respect to the hiring of any persons whose resumes are so submitted and are not eligible for placement fees. Avalo Therapeutics is a clinical stage biotechnology company fully dedicated to developing therapeutics targeting the IL-1 pathway for immune-mediated inflammatory diseases.
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.
Senior Director, Translational Medicine & Early Clinical Development Madrigal Pharmaceuticals IncSenior Director, Translational Medicine & Early Clinical DevelopmentConshohocken, PA$259,000–$317,000 / yearPlease know that Madrigal does not conduct interviews via text or in chat rooms; conduct interviews via Skype, RingCentral or solely via telephone; charge candidates an advance fee of any kind (e.g., fees for purchasing equipment); nor does it offer positions of employment without undergoing a thorough recruiting process. The Senior Medical Director, Translational Medicine & Early Clinical Development is a senior physician-scientist responsible for leading early development and mechanistic clinical studies and shaping the translational strategy across Madrigal's metabolic liver and cardiometabolic portfolio.
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.
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 Quality Control Reviewer Integrated Resources, IncClinical Quality Control ReviewerCollegeville, PennsylvaniaContractorIT Life Sciences Allied Healthcare CROCertified MBE |GSA - Schedule 66 I GSA - Schedule 621IDirect:732-429-1921 (Tel) 732-549-2030*241 | (F) 732-549-5549Gold Seal JCAHO Certified for Health Care Staffing"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row) Job DescriptionResponsibilities:Data Quality Review / Quality Control (DQR/QC): - Independently performs DQR/QC on clinical components of assigned documents (eg, clinical study reports, investigator brochures, manuscripts, summary documents, regulatory responses, etc.).Formally documents findings of assigned documents.
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 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.
Sr. Principal Scientist, Clinical Operations Immunology Lead Merck & Co IncSr. Principal Scientist, Clinical Operations Immunology LeadWest Point, PA$210,400–$331,100 / yearIn a competitive external landscape and fast-paced internal environment, the Immunology Clinical Operations Lead position provides both strategic and operational leadership across early immunology programs, ensuring timely, high-quality execution of clinical studies and clinical pharmacology strategies worldwide. Translational Medicine (TMed) drives early clinical development of novel therapeutics by partnering with Discovery Sciences and Late-Stage Clinical Research to translate scientific discoveries into human proof-of-concept and advance the most promising candidates through the pipeline to patients.
NewClinical 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.
Associate Director, Clinical Operations Harmony Biosciences Holdings IncAssociate Director, Clinical OperationsPlymouth Meeting, PAPrepares and/or reviews study-related and essential clinical study start-up documents (e.g., Clinical protocols, Informed consent forms, Investigator Brochures, Pharmacy Manual, Monitoring Plan, Laboratory Manual, Patient Diary, Clinical Site Procedures Manual, Pharmacy Manual, Case Report Form (CRFs), CRF Completion Guidelines and other relevant study plans and charters). Responsibilities include but are not limited to: Responsible for the oversight of trial-level operations for existing and/or future clinical studies, including but not limited to protocol concept design, CRO and vendor selection, CRO oversight, investigator meetings, etc.
Clinical Technology Sales Representitive IQVIA Holdings IncClinical Technology Sales RepresentitiveWayne, PA$89,600–$249,600 / yearThis role focuses on business creation, account expansion, and strategic customer engagement, partnering closely with IQVIA clinical, operational, and technical teams to deliver technology‑enabled solutions for complex clinical trials. Build and maintain strong, long‑term relationships with key sponsor decisionmakers and influencers, developing a deep understanding of customer organizations, business needs, study pipelines, and technology strategies.
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).
SR. CLINICAL DATA MANAGER Calsoft LabsSR. CLINICAL DATA MANAGERKING OF PRUSSIA, PA$96,013 / yearProvide clear verbal or written information and hands-on support to project team members and to CROs related to eCRF and database design, data quality, and reporting of database / data quality status. • Serve as the DM study lead and the primary point of contact for clinical study teams and external partners, (e.g., external data vendors and CROs) for multiple trials within a given TA.
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.