Clinical Research Coordinator I (PA/NJ residents only) St. Luke's Health Network, Inc.Clinical Research Coordinator I (PA/NJ residents only)Bethlehem, PAFull timeIndividually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care. Bachelor’s degree required; will accept Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience highly preferred.
NewPractice Pediatric Allergy and Immunologist with UPMC in Pittsburgh, PA UPMC Southwestern PAPractice Pediatric Allergy and Immunologist with UPMC in Pittsburgh, PAAlbany Township, PennsylvaniaMultiple subspecialty areas of focus, with an established multispecialty Asthma Center and Severe Asthma Clinic and a multispecialty research and clinical center caring for patients with inborn errors of immunity in our Pittsburgh Immunogenetics Discovery Center. Serve a large and diverse community of patients in western Pennsylvania and beyond with asthma, allergies, eczema and inborn errors of immunity with well-established sub-specialty and multidisciplinary clinics for severe asthma, eczema, eosinophilic esophagitis, and immunodeficiency.
Research Assistant I - Analytical Chemistry Charles River Laboratories International IncResearch Assistant I - Analytical ChemistryPA$23–$24 / hourFrom individual specialty toxicology and IND enabling studies to tailored packages and total laboratory support, our deeply experienced team can design and execute programs that anticipate challenges and avoid roadblocks for a smooth, efficient journey to market. If you are interested in applying to Charles River Laboratories and need special assistance or an accommodation due to a disability to complete any forms or to otherwise participate in the resume submission process, please contact a member of our Human Resources team by sending an e-mail message to crrecruitment_US@crl.com.
Executive Director, Product Development Team Leader, Clinical Research, Hematology Merck & Co IncExecutive Director, Product Development Team Leader, Clinical Research, HematologyNorth Wales, PA$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.
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.
NewPrin. 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 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 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.
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. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
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.
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.
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.
Clinical Research Nurse Tower HealthClinical Research NursePhoenixville, PennsylvaniaFull timeAdditionally, the system provides a wide range of healthcare services, such as Reading Hospital Rehabilitation at Wyomissing, home healthcare via Tower Health at Home, TowerDirect ambulance and emergency response, Tower Health Medical Group, Tower Health Providers (a clinically integrated network), and Tower Health Urgent Care facilities across its service area. Committed to academic medicine and training, Tower Health offers various programs, including residency and fellowship programs, the Drexel University College of Medicine at Tower Health, and the Reading Hospital School of Health Sciences.
Associate Principal Scientist, Clinical Research Merck & Co IncAssociate Principal Scientist, Clinical ResearchWest Point, PA$142,400–$224,100 / yearTranslational 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. Leads and directs teams through key study planning, development, and execution activities, including program overviews, issue escalation and mitigation, senior management presentations, cross-functional governance meetings, and advisory meeting preparation.
Clinical Research Coordinator I (PA/NJ residents only) St. Luke's University Health NetworkClinical Research Coordinator I (PA/NJ residents only)Bethlehem, PAIndividually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care. EDUCATION: Bachelor's degree required; will accept Associates degree or High School degree with equivalent clinical research experience (3 years) with 1-2 years coordinator and/or data management experience highly preferred.
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.
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.
Clinical Research Nurse Tower Health Medical GroupClinical Research NursePhoenixville, PAAdditionally, the system provides a wide range of healthcare services, such as Reading Hospital Rehabilitation at Wyomissing, home healthcare via Tower Health at Home, TowerDirect ambulance and emergency response, Tower Health Medical Group, Tower Health Providers (a clinically integrated network), and Tower Health Urgent Care facilities across its service area. The role of the Clinical Research Nurse (CRN): Facilitates and coordinates clinical research studies as part of a multidisciplinary team with roles and responsibilities involving regulatory document processing, interactions with sponsors and Contract Research Organizations (CRO) as well as Institutional Review Boards.
NewSr. Clinical Research Associate ICON PlcSr. Clinical Research AssociateBlue Bell, CA$110,520–$138,150 / yearWilling and able to travel up to 50% for on-site monitoring visits across the West region; preference given to candidates residing near major HUB airport to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research Associate II ICON PlcClinical Research Associate IIBlue Bell, PA$91,336–$114,170 / yearWilling and able to travel up to 50% for on-site monitoring visits across the West region; preference given to candidates residing in Los Angeles, Phoenix, Seattle, Denver or Portland, near major HUB airports to support efficient regional travel. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Clinical Research IRT Project Manager ICON PlcClinical Research IRT Project ManagerBlue Bell, PARemotePrior User Acceptance Testing (UAT) experience within IRT systems which includes writing/executing UAT test scripts and completing UAT documentation. Your expertise will be vital in ensuring that IRT systems are developed and deployed effectively to support project timelines and enhance operational efficiency.
Part-Time Research Assistant Entomology Pennsylvania State UniversityPart-Time Research Assistant EntomologyLehigh County, PAPenn State Extension Lehigh County is seeking applicants for a part-time research assistant position to support research on the biological control of spotted-wing drosophila (SWD), Drosophila suzukii, in Pennsylvania small fruit production systems. Pursuant to the Jeanne Clery Disclosure of Campus Security Policy and Campus Crime Statistics Act and the Pennsylvania Act of 1988, Penn State publishes a combined Annual Security and Annual Fire Safety Report (ASR).
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).
FSP Senior Research Scientist-Dissolution Method Development Thermo Fisher Scientific IncFSP Senior Research Scientist-Dissolution Method DevelopmentCollegeville, PAWithin our Analytical Services team, we have a functional service provider solution, which is an outstanding partnership that allows our customers to use the experience of our staff, while allowing you, the employee, to gain direct experience working onsite at a pharmaceutical/ biopharmaceutical company, all while maintaining full-time benefits. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services.
Research Technician IV ICON PlcResearch Technician IVBlue Bell, PA$68,616–$85,770 / yearResearchers in this group express, purify and crystalize ESKAPEE pathogen proteins of interest and utilize sophisticated techniques such as X-ray Crystallography and mass spectroscopy to model small molecule drug-protein interactions. Performs microbiological and molecular biological studies on various bacterial pathogens of military relevance under biosafety level 2 and 3 conditions, including genetic/genotypic analysis of these pathogens.
Non-Interventional Study Research Manager ICON PlcNon-Interventional Study Research ManagerBlue Bell, PAAs a Non-Interventional Study Research Manager at ICON, you will manage clinical trial operations activities, supporting your team and stakeholders to deliver high-quality outcomes across our clinical programs. ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
Research Finance Coordinator II St. Luke's University Health NetworkResearch Finance Coordinator IIAllentown, PALuke''s and affiliated providers with billing coverage analysis template development, assist in the preparation of clinical trial cost analyses for new trials based on non-billable expenses and personnel resource time and effort, identifying the research charges to be utilized in budget development based on set institutional research floor rates, preparation and tracking of invoices, tracking revenue and expenses in the department's financial database, as well as creating and maintaining study folders and financial binders for all active clinical trials. Individually and together, our employees are dedicated to satisfying the mission of our organization which is an unwavering commitment to excellence as we care for the sick and injured; educate physicians, nurses and other health care providers; and improve access to care in the communities we serve, regardless of a patient's ability to pay for health care.
Principal Scientist (Director) - Outcomes Research Merck & Co IncPrincipal Scientist (Director) - Outcomes ResearchNorth Wales, PA$190,800–$300,300 / yearPrimary Responsibilities: This position has primary responsibility for planning/managing a comprehensive program of real-world evidence and non-interventional research activities for in-line and pipeline products for lung cancers to meet the value evidence needs of clinicians, payers, policymakers, health technology assessment (HTA)/reimbursement agencies, and health systems globally. The following skills and knowledge are needed to be successful in this role: Decision making: Identifying and understanding problems and opportunities by gathering, analyzing and interpreting quantitative and qualitative information; choosing the best course of action by establishing clear decision criteria, generating and evaluating alternatives, and making timely decisions; taking action that is consistent with available facts and constraints and optimizes probable consequences.
Director, Global Real-World Evidence & Health Outcomes Research Scientist, Hematology-Oncology GSK plcDirector, Global Real-World Evidence & Health Outcomes Research Scientist, Hematology-OncologyCollegeville, PA$185,250–$308,750 / yearThe role of Director, Global Real-World Evidence & Health Outcomes Research Scientist Hematology-Oncology ensures that each medicine GSK brings to market is supported by scientifically credible, high quality evidence that drives competitiveness and strong evidence-based product positioning, value propositions, and value-based pricing. Develop and maintain a good working knowledge of real-world data resources, existing partnerships and public initiatives and become the point person for select sources to advise on their suitability to address given research questions.
Associate Director, Outcomes Research Merck & Co IncAssociate Director, Outcomes ResearchNorth Wales, PA$156,900–$247,000 / yearUnder the guidance of a senior leader, an Associate Principal Scientist/Associate Director, has primary responsibility for planning/managing real world and economic evidence activities for in-line and pipeline products to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient reported outcomes assessments, systematic reviews and meta-analyses, and economic modelling.
Associate Principal Scientist (Associate Director) - Outcomes Research - Hematology Merck & Co IncAssociate Principal Scientist (Associate Director) - Outcomes Research - HematologyNorth Wales, PA$156,900–$247,000 / yearPrimary Responsibilities: This position has primary responsibility for planning/managing of real-world evidence and non-interventional research activities for in-line and pipeline products in hematology to meet the value evidence needs of clinicians, payers, policymakers, health technology assessment (HTA)/reimbursement agencies, and health systems globally. In collaboration with internal teams and external partners, design non-interventional and data synthesis studies, author study protocols, develop measurement questionnaires, case report forms, data analysis plans, final study reports, scientific presentations, and publications.
Finite Element (FEA) Research Engineer Globus Medical IncFinite Element (FEA) Research EngineerPAEssential Functions: Develops advanced computational protocols and finite element models in collaboration with surgeons and researchers; specifically, plans and executes general and patient-specific spinal simulations to identify pros/cons in clinical treatments to optimize surgical outcomes in musculoskeletal fields. Position Summary: The Finite Element (FEA) Research Engineer will be responsible for leading computational simulation efforts, including the development, validation, and execution of FEA models for spine (and/or trauma and joint reconstruction) to address unmet clinical needs.
Postdoctoral Research Associate in the Department of Biostatistics & Health Data Science Lehigh UniversityPostdoctoral Research Associate in the Department of Biostatistics & Health Data ScienceBethlehem, PAShe is an Assistant Professor jointly appointed in Civil & Environmental Engineering and Population Health at Lehigh University, where her work includes sustained engagement with water, sanitation, and hygiene (WASH) challenges in humanitarian and development contexts, which serve as important contexts for broader questions about environmental transmission, system resilience, and the real-world performance of public health interventions. Areas of expertise include bioinformatics, computational biology, artificial intelligence, network science, Bayesian methods, spatiotemporal methods, visualization, evolutionary game theory, infectious disease modeling, and assistive and accessibility technologies, with a shared commitment to improving health outcomes through data-driven discovery.
Postdoctoral Research Associate in Evolutionary Cell Biology Lehigh UniversityPostdoctoral Research Associate in Evolutionary Cell BiologyBethlehem, PAThe incoming postdoctoral researcher will lead experimental projects on the evolutionary mechanisms of chromosome segregation in mammals, using mouse oocytes, preimplantation embryos, hybrid mouse models, and/or tissue culture cells. Qualifications: Doctoral degree (or near completion) in cell biology, molecular biology, genetics, developmental biology, or evolutionary biology, or a closely related field, completed by the start of the appointment.
Project Manager, Research Translation Acceleration Lehigh UniversityProject Manager, Research Translation AccelerationBethlehem, PA$83,910–$102,080 / yearAs Project Manager for Research Translation Acceleration, you''ll drive the operations of a nationally recognized NSF-funded ART grant, helping Lehigh shape how research moves from the lab into the hands of people who need it most. Serve as the primary liaison for internal departments, external mentors, and peer NSF ART-funded institutions, while managing the logistics for seminars, workshops, and major conferences.
Research Project Manager Lehigh UniversityResearch Project ManagerBethlehem, PA$67,270–$81,830 / yearWork closely with PIs and project teams to plan, organize, and execute internally/externally funded projects; continuously develop, refine, and maintain project plans, management processes, and tools to improve efficiency, communication, sustainability, and steady progress. If you bring deep experience in grant management, a collaborative instinct, and the organizational discipline to keep complex initiatives on track, this role puts you at the center of meaningful, funded research at one of the nation''s leading research universities.
Postdoctoral Research Associate in Evolutionary Genomics & Molecular Evolution Lehigh UniversityPostdoctoral Research Associate in Evolutionary Genomics & Molecular EvolutionBethlehem, PAThe ideal candidate will also be willing to perform fieldwork to collect marine organisms, including but not limited to day-long or extended (seven - thirty day) research cruises, and field trips to remote stations. Additional skills that are helpful but no required include FACS, fieldwork, protein purification, fluorescence and expansion microscopy, rearing animals in aquaria, and invertebrate transgenics.
Coordinator, Research Translation Lehigh UniversityCoordinator, Research TranslationBethlehem, PA$19,840–$23,810 / yearJoin Lehigh University''s Office of Vice Provost for Research as an ART Coordinator supporting our groundbreaking NSF Accelerating Research Translation (ART) initiative and Research Translation Accelerator (RTA). You''ll coordinate day-to-day activities across multiple workstreams, ensuring seamless execution of meetings, events, communications, stakeholder engagement, and project documentation that align with our program goals.
Senior Account Manager - Market Research (Remote) M3 USA CorpSenior Account Manager - Market Research (Remote)PARemoteM3 services incorporate all of the most advanced statistical and attitudinal methodologies allowing clients to provide world-class offerings and support services to their end-client customers throughout multiple industry sectors. About the Business Unit: M3 Global Research, part of M3 Inc., provides the most comprehensive and highest quality market research recruitment and support services available to the industry with relationships reaching respondents in more than 70 countries worldwide.
Senior Account Manager - Market Research (Remote) M3 Global Research (US)Senior Account Manager - Market Research (Remote)Fort Washington, PARemoteM3 services incorporate all of the most advanced statistical and attitudinal methodologies allowing clients to provide world-class offerings and support services to their end-client customers throughout multiple industry sectors. M3 Global Research maintains ISO 20252 and 27001 certifications with the highest quality data collection and project management capabilities that cover the spectrum of quantitative and qualitative techniques utilized today.
Postdoctoral Research Associate - Farming Systems Trial Rodale InstitutePostdoctoral Research Associate - Farming Systems TrialKutztown, PennsylvaniaThis position offers an exciting opportunity to integrate field measurements, long-term datasets, and process-based models (DayCent, DNDC, or similar) to evaluate management-driven changes in soil carbon storage, nitrogen cycling, and greenhouse gas emissions. The successful candidate will work at the interface of soil process modeling, carbon cycling, and regenerative organic farming systems, contributing to projects that quantify soil health improvements and carbon–nitrogen dynamics under contrasting management systems.
Postdoctoral Research Associate - Vegetable Systems Trial Rodale InstitutePostdoctoral Research Associate - Vegetable Systems TrialKutztown, PennsylvaniaAs the Vegetable Systems Trial enters a new phase, this position offers the opportunity to straddle these phases by utilizing existing long-term data collected from the Vegetable Systems Trial and other multidisciplinary research projects, as well as engage with new projects that include deeper nutrient and soil testing. The Postdoctoral Research Associate will assist with coordinating field trials, data collection, processing samples, analyzing data, preparing peer-reviewed journal articles, and presenting research findings at regional and national conferences.
CMBS / CRE Research - Associate PA Kroll Bond Rating Agency Inc.CMBS / CRE Research - Associate PAPA$90,000–$110,000 / yearThis role will work closely with the Senior Researcher, as well as modeling, new issue and surveillance teams, to produce high-quality research, data analysis, and publications that inform market participants and support KBRA's ratings process. Summary/Overview: Kroll Bond Rating Agency (KBRA)'s CMBS group is seeking a highly motivated CMBS / CRE Research Associate to support the firm's commercial real estate (CRE) and CMBS platform.
Clinical Trial Associate ICON PlcClinical Trial AssociateBlue Bell, PAAs a SMA II at ICON, you will support the management and monitor of clinical trial sites by ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. Key responsibilities include: Coordinating monitoring activities at clinical trial sites, ensuring adherence to study protocols and timely resolution of site-related issues.
Director, Clinical Science, Cronos IQVIADirector, Clinical Science, CronosBethlehem, PennsylvaniaCronos combines deep clinical and scientific expertise with advanced clinical analytics, proprietary technology platforms and scalable global delivery models to support a broad range of therapeutic areas, partnering flexibly with sponsors, IQVIA CRO teams, and external CROs to reduce variability, prevent measurement risk, and enable more conclusive clinical research outcomes. Cronos is IQVIA’s global clinical outcome assessment and rater services business within the Patient‑Centered Solutions and Connected Technologies (PACT) business, providing scientifically rigorous rater training, certification, monitoring, and data quality oversight to improve endpoint reliability in clinical trials.
Medical Director, Clinical Development Johnson and JohnsonMedical Director, Clinical DevelopmentSpring House, PAFull timeWorks in close partnership with the Compound Development Team (CDTL) and project management, global regulatory affairs, clinical pharmacology, health economics, and the disease area leader to share information. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Director, Clinical Science, Cronos IQVIA Holdings IncDirector, Clinical Science, CronosBethlehem, PACronos combines deep clinical and scientific expertise with advanced clinical analytics, proprietary technology platforms and scalable global delivery models to support a broad range of therapeutic areas, partnering flexibly with sponsors, IQVIA CRO teams, and external CROs to reduce variability, prevent measurement risk, and enable more conclusive clinical research outcomes. Cronos is IQVIA's global clinical outcome assessment and rater services business within the Patient‑Centered Solutions and Connected Technologies (PACT) business, providing scientifically rigorous rater training, certification, monitoring, and data quality oversight to improve endpoint reliability in clinical trials.
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).
Senior CRA ICON PlcSenior CRABlue 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.