Per Diem Lead Dosing Session Monitor Adams ClinicalPer Diem Lead Dosing Session MonitorPhiladelphia, PennsylvaniaWe are seeking a P er Diem Lead Dosing Monitor/Therapist for exciting clinical trials focused on psychedelic research for individuals with depression, anxiety, and other mood disorders at one or moreofour researchsitelocations. Guided by our core values— Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration —we create an environment where meaningful work drives meaningful change.
Pulmonary Intensivist Sleep Physician Temple University Health SystemPulmonary Intensivist Sleep PhysicianPhiladelphia, PAPennsylvania-Philadelphia'',''Pennsylvania-Philadelphia'',''Research Faculty'',''Research Faculty'',''Full-time'',''Full-time'',''Day Job'',''Day Job'',''Regular'',''Regular'',''false'',''406979'',''406979'',''true'',''406979'',''false'',''Submission for the position: Pulmonary Intensivist Sleep Physician - (Job Number: 264316)'',''false'',''406979'',''false'',''true''. Temple Health consists of Temple University Hospital (TUH), Fox Chase Cancer Center, TUH-Jeanes Campus, TUH-Episcopal Campus, TUH-Northeastern Campus, Temple Physicians, Inc., and Temple Transport Team.
Clinical Informaticist Virtua Health IncClinical InformaticistNJ$93,152–$149,438 / yearSummary: The Clinical Informaticist collaborates with organizational leaders and system end users, across the continuum of care to support the successful clinical transformation, IT governance, adoption, and interoperability of clinical systems. The Clinical Informaticist, with guidance from Senior and Lead Clinical Informaticists, engages in IT projects and optimizations by utilizing process improvement and change management methodologies to carry out operational readiness strategies.
Senior Director, Quantitative Pharmacology Sun Pharmaceutical Industries LtdSenior Director, Quantitative PharmacologyPrinceton, NJ$215,500–$239,500 / yearThe Quantitative Pharmacology group is responsible for the oversight over drug development aspects related to clinical pharmacology and pharmacometrics of clinical development candidates, working in close collaboration with nonclinical and clinical functional areas. Development and execution of model-based analyses including translational PK/PD approaches, population pharmacokinetic models, exposure-response models, clinical trial design simulations, and quantitative systems pharmacology (QSP) modeling.
Interventional Study Scientist Medical Director GSK plcInterventional Study Scientist Medical DirectorCollegeville, PA$187,275–$312,125 / yearAs a member of Medical Affairs organisation, you'll collaborate with cross-functional teams to shape clinical practice, engage with healthcare professionals, and deliver on our promise to help people do more, feel better, and live longer. Please note that if you are a US Licensed Healthcare Professional or Healthcare Professional as defined by the laws of the state issuing your license, GSK may be required to capture and report expenses GSK incurs, on your behalf, in the event you are afforded an interview for employment.
2027 Future Talent Program - Clinical and Regulatory Strategic Communications - Intern Merck & Co Inc2027 Future Talent Program - Clinical and Regulatory Strategic Communications - InternNorth Wales, PA$39,908–$111,111 / yearClinical Regulatory & Strategic Communications (CRSC) is a multidisciplinary organization that plays a critical role in supporting the development of new medicines by creating key clinical and regulatory documents, communicating clinical trial results, and ensuring information is shared responsibly and transparently with regulatory agencies, healthcare professionals, trial participants, and the public. Seeking a highly motivated individual who is pursuing an education in the life sciences, medicine, pharmacology/pharmacy, quality, operations, data science, or a related field, and who is interested in writing, communicating about medicine and science, and supporting the quality, compliance and operational excellence activities that enable clinical research.
Quality Specialist I Logistics Parexel International CorpQuality Specialist I LogisticsQuakertown, PAWith 22,000+ employees worldwide, we partner with biopharmaceutical companies and research sites to design and deliver patient-focused clinical trials that broaden access and make research a care option for anyone, anywhere. With diverse teams and continuous learning opportunities, the Quality Specialist I can explore career paths and expand skills across clinical research and supply chain operations.
2026 Future Talent Program - Clinical Safety Risk Management - Intern Merck & Co Inc2026 Future Talent Program - Clinical Safety Risk Management - InternNorth Wales, PAThrough this experience, the intern may assist with organizing and analyzing safety-related information, supporting documentation or training materials, identifying opportunities to simplify team processes, and exploring how digital tools-including AI-enabled approaches-can help improve the way work is performed. Clinical Safety and Risk Management (CSRM) is an international, diverse team dedicated to advancing the safe use of our products through proactive safety surveillance, effective risk management, and transparent communication across all phases of the product lifecycle.
Clinical Genetic Intake Coordinator Temple University Health SystemClinical Genetic Intake CoordinatorPhiladelphia, PAThe Clinical Genetic Intake Coordinator is responsible for the registration and scheduling of patients to the Department of Clinical Genetics, ensuring that all required patient information is collected and entered into our research database as well as into our EPIC EMR system at the time of appointment scheduling. Clerical duties include, but are not limited to, chart creation, medical record collection, data entry, insurance verification, and delivery of excellent customer service via phone to patients and referring providers.
Clinical Coordinator - Episcopal Campus - Pool Temple University Health SystemClinical Coordinator - Episcopal Campus - PoolPhiladelphia, PAAssists the Directors of Nursing and Nurse Managers in continuous staff development, human resource management, and in promoting quality care. Directs and collaborates with appropriate department managers to facilitate and expedite patient movement.
Mental Health Technician Adams ClinicalMental Health TechnicianPhiladelphia, PA$22–$25 / hourThis position supports ongoing clinical trials by providing direct care, supervision, and engagement with research participants under the guidance of the In-patient Unit Manager, Clinical Research Coordinators, and the Principal Investigator. Guided by our core values—Scientific Rigor, Operational Excellence, Commitment to Sponsors and Participants, and Authentic Collaboration—we create an environment where meaningful work drives meaningful change.
Medical Director, Clinical Development Organon & CoMedical Director, Clinical DevelopmentPlymouth Meeting, PARemote$204,100–$347,300 / yearRepresent clinical development on study teams, collaborating closely with clinical operations and team members in identifying clinical study issues, barriers to execution, and developing sound strategic solutions with partners of the study team to ensure timely resolution. Work closely with Operations and vendor to identify and/or vet sites for clinical trial participation Design patient-centered clinical protocols that support strategic objectives, are feasibly conducted, and support efficient recruitment to meet program timelines.
Clinical Lead Eagleville HospitalClinical LeadPALeads the team in assuring that the program schedule meets the needs of the patients and is followed daily to ensure effective treatment. Evaluates staffing needs and works with nurse managers to ensure adequate staffing for acuity and programming.
NewClinical Coordinator Pool, Rotating Shifts, Capacity Management Ctr, Women And Families Campus Temple University Health SystemClinical Coordinator Pool, Rotating Shifts, Capacity Management Ctr, Women And Families CampusPhiladelphia, PATo be considered for this position, candidates must have a minimum of 1 year experience in the Emergency Department or Intensive Care Units (after orientation training), and have experience participating in or running rapid response/ code teams. Assists the Directors of Nursing and Nurse Managers in continuous staff development, human resource management, and in promoting quality care.
Evidence Generation Manager ZSEvidence Generation ManagerPrinceton, New Jerseynbsp: This role will work directly within the Medical & Evidence Generation space, partnering closely with stakeholders across Drug Development, Clinical Operations, Real-World Evidence (RWE), Medical Affairs, Payers, Providers, and Biopharmaceutical organizations to design and execute high-impact strategic and operational initiatives that accelerate evidence generation and improve healthcare outcomes. • Drive strategic business development activities, including identifying opportunities, building executive relationships, developing proposals, and expanding client partnerships across R&D, Clinical Development, Medical Affairs, and Evidence Generation.
Senior Medical Director, Oncology Clinical Development - Sarcoma GSK plcSenior Medical Director, Oncology Clinical Development - SarcomaCollegeville, PA$284,250–$473,750 / yearClinical Data Interpretation, Clinical Pharmacology, Clinical Trial Designs, Clinical Trials Monitoring, Digital Fluency, Drug Development, Drug Regulatory Affairs, Evidence Based Decision Making, Executive Presence, Hematology and Oncology, Learning Agility, Matrix Leadership, Real World Evidence (RWE), Scientific Presentations, Strategic Direction. Operating within the clinical strategy defined by the Clinical Development Lead (CDL), the Senior Medical Director partners closely with the Senior Scientist and cross-functional teams to guide the integration of physician expertise into study execution and programme-level decision-making.
NewTrauma Clinical Nurse Coordinator, Full Time, 7A-3:30P Temple University Health SystemTrauma Clinical Nurse Coordinator, Full Time, 7A-3:30PPhiladelphia, PACollaborates with the Trauma Director and Trauma Program Manager on clinical components of the Trauma Program. 5 years experience in trauma, critical care or emergency department Required.
Senior Manager, R&D Procurement - Clinical Labs and Diagnostics GSK plcSenior Manager, R&D Procurement - Clinical Labs and DiagnosticsCollegeville, PA$113,850–$189,750 / yearAs a Senior R&D Procurement Manager in Clinical Services, you will be accountable for a category of outsourced services needed for GSK's clinical trials: Negotiate contracts with suppliers that secure favorable terms for procurement of goods and services contracts in line with the agreed business requirements. This role will provide YOU the opportunity to lead key activities to progress YOUR career, these responsibilities include some of the following: Accountability for end-to-end management of the Medicines Specialty Labs and Companion Diagnostics categories.
Clinical Care Technician - Oncology Unit - Part Time Night RWJ Barnabas Health Medical IncClinical Care Technician - Oncology Unit - Part Time NightSomerville, NJ$21.04–$26.19 / hourAs a Clinical Care Technician (CCT), a typical day may include: Assisting patients with activities of daily living and providing nursing care to patients including taking vital signs, EKGS, performing phlebotomy, assisting with bedside care, i.e. bathing, mouth care, skin care. As a Clinical Care Technician (CCT), you will be a vital part of our collaborative nursing team, supporting Registered Nurses in providing hands-on care and helping create a safe, welcoming environment for patients.
Clinical Product Data Management Lead Dale Workforce SolutionsClinical Product Data Management LeadWayne, PARemoteWe are seeking an experienced Clinical Product Data Management Lead to provide leadership, guidance, and oversight for a newly forming clinical product data management team. The strongest candidates will have direct experience managing clinical product master data within a large pharmaceutical or biotech organization and understand the evolution of product data from molecule/compound development through commercialization.