Clinical Research Assistant-Recruitment Temple UniversityClinical Research Assistant-RecruitmentPhiladelphia, Pennsylvania$49,000The Clinical Research Assistant works under the direct supervision of the Principal Investigator and/or other Research Coordinators and will assist with specific research tasks associated with clinical research projects or clinical trials. The Temple University's Lewis Katz School of Medicine's TMS-Pulm/Critical Care/SleepMed Department is searching for a Clinical Research Assistant-Recruitment to join our team!
Clinical Research Postdoctoral Fellow - Mitochondrial Myopathy Children's Hospital of PhiladelphiaClinical Research Postdoctoral Fellow - Mitochondrial MyopathyPhiladelphia, PAThis role would provide opportunity for data collection, conduct independent scholarly research and develop new methods and protocols, participate in project planning, recording and evaluation of data, learn to conduct statistical analyses under supervision of a biostatistician, acquire manuscript and grant writing skills, participate in seminars, lectures, poster sessions and presentation at meetings, supervise junior lab members, and multidisciplinary team coordination. We are seeking motivated individuals to make an academic contribution to the Mitochondrial Myopathy Clinical Research program, which focuses on validation of objective outcome measures in Mitochondrial Myopathy for natural history studies and clinical trials in its clinical research effort, and human subjects in translational research efforts.
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.
Director (Principal Scientist), Clinical Research, Respiratory Merck & Co IncDirector (Principal Scientist), Clinical Research, Respiratoryupper gwynedd, PA$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 Cardiovascular and Respiratory therapeutic area.
Clinical Research Regulatory Specialist - Profound Autism Research Study and Orphan Disease Center Children's Hospital of PhiladelphiaClinical Research Regulatory Specialist - Profound Autism Research Study and Orphan Disease CenterPhiladelphia, PA$76,100–$97,000 / yearThis position is responsible to assist with the preparation, review, and submission of all protocols, amendments, informed consent documents, annual This position is responsible for assisting with the preparation, review, and submission of all protocols, amendments, informed consent documents, annual reviews and safety reports to the IRB for a large-scale longitudinal research project spanning multiple departments, including Developmental Behavioral Pediatrics, Neurology, Genetics, and the Center for Autism Research at Children's Hospital of Philadelphia. This ideal candidate must be knowledgeable on, have full understanding of, and promote good clinical practices (GCP) and will be held accountable for adherence to all policies and procedures surrounding these processes and for maintaining up to date knowledge on these policies from IRB, FDA, ICH, GCP, or other sources.
Clinical Trial Supply (CTS) Study Manager CSL Behring LLCClinical Trial Supply (CTS) Study ManagerKing of Prussia, PAWe use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
Clinical Research Coordinator C (OBGYN - Pregnancy and Perinatal Research Center) University of PennsylvaniaClinical Research Coordinator C (OBGYN - Pregnancy and Perinatal Research Center)Philadelphia, PA$63,085–$67,046 / yearThe essential functions of the position include, but are not limited to: Serve as a senior clinical research coordinator for the NIH Environmental influences on Child Health Outcomes (ECHO) Program, independently managing complex protocol activities and participant follow-up with minimal supervision. Long-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility.
Associate Scientist, Clinical Services (Onsite) Merck & Co IncAssociate Scientist, Clinical Services (Onsite)West Point, PA$71,900–$113,200 / yearOur company a global healthcare leader, is currently seeking an entry-level Veterinary Associate to join our collaborative, dynamic, and inclusive Laboratory Animal Science Team at the West Point location. Collaborate effectively as a team player with principal investigators, scientific staff, veterinarians, veterinary technicians, IACUC members, facility managers, and animal care technicians.
Registered Nurse Clinical Research Coordinator Cardiology Consultants of PhiladelphiaRegistered Nurse Clinical Research CoordinatorPhiladelphia, PAPart timeClinical Research, Cardiology Practice, Cath Lab, EP Lab, Telemetry Floor; Intensive Care Unit; Cardiac Care Unit; Emergency Room, etc.). Perform cardiovascular patient assessments and collect data for research studies that involve new cardiac devices and drugs in office and hospital settings.
Senior Clinical Project Manager ICON PlcSenior Clinical Project ManagerBlue Bell, PARemoteExtensive experience in project management, with a proven track record of leading successful projects in the pharmaceutical or biotech industry; experience in oncology, nuclear medicine, radiopharmaceuticals, or radioligand therapies is strongly preferred. As a Senior Clinical Project Manager at ICON, you will be responsible for leading and manage projects, ensuring successful execution and delivery of project objectives, including those supporting radiopharmaceutical and radioligand-based clinical programs.
NewSenior Clinical Project Manager (Hem/Onc) ICON PlcSenior Clinical Project Manager (Hem/Onc)Blue Bell, PARemoteAs a Senior Clinical Project Manager at ICON, you will be responsible for full-scope project management, ensuring successful execution and delivery of project objectives, including those supporting radiopharmaceutical and radioligand-based clinical programs. Staying abreast of industry trends and emerging technologies, including advancements in precision medicine, radiopharmaceuticals, and targeted oncology therapies, to integrate best practices into project management strategies.
Clinical Research Coordinator B University of PennsylvaniaClinical Research Coordinator BPA$53,418–$58,059 / yearLong-Term Care Insurance: In partnership with Genworth Financial, Penn offers faculty and staff (and your eligible family members) long-term care insurance to help you cover some of the costs of long-term care services received at home, in the community or in a nursing facility. In addition to the duties listed above for the CRC A, the CRC B will be responsible for creating invoices, independently preparing and submitting IRB documents, training and delegating tasks to other coordinators, and cleaning/submitting large data sets to study databases.
Senior Clinical Trial Manager ICON PlcSenior Clinical Trial ManagerBlue Bell, PAClose collaboration with the assigned Local Trial Manager(s) (LTMs), Lead Site Manager (LSM), Site Managers (SMs), Clinical Trial Associates (CTAs), and Site Contract Managers (SCMs) to outline accountabilities/responsibilities and provide support and training, where necessary. The Sr LTM will manage and oversee the following throughout the study: Central IRB and other local vendors (Greenphire, Drug Destruction services, etc.…) including set up of vendor purchase orders, invoice review and approval, and change-orders, as applicable.
Clinical Scientist Integrated Resources, IncClinical ScientistCollegeville, PennsylvaniaContractorCoordinating and leading the investigation process on all manufacturing and laboratory incidents related to all deviations including biomanufacturing process and equipment deviations and deviations for all analytical assays. A 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.
Senior Principal Scientist, Clinical Research, Thoracic Malignancies Merck & Co IncSenior Principal Scientist, Clinical Research, Thoracic MalignanciesNorth 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.
Clinical Trial Research Monitor II Fox ChaseClinical Trial Research Monitor IIPhiladelphia, PATemple 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. To support this mission, Temple Health is continuously recruiting top talent to join its diverse, 10,000 strong workforce that fosters a healthy, safe and productive environment for its patients, visitors, students and colleagues alike.
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.
Clinical Research Associate 1 Allen SpoldenClinical Research Associate 1Philadelphia, PennsylvaniaConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.
NewSenior Clinical Research Associate IRESenior Clinical Research AssociatePhiladelphia, PennsylvaniaPerform remote and on-site monitoring/co-monitoring visits (Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits and Close-Out Visits) to ensure data integrity and subject safety in the client's trials. CRA role will support the client's Oncology clinical trials to ensure data integrity, subject safety, and inspection readiness at the clinical investigative sites.
Clinical Research Associate II Allen SpoldenClinical Research Associate IIPhiladelphia, PennsylvaniaConduct ongoing study monitoring, including frequent periodic site visits, protocol adherence checks, material handling procedures, inspection of study files, and related monitoring functions. Initiate studies performing initiation site visits, arrange for shipment of clinical supplies, case report forms, and other necessary materials.