Clinical Specialist JouléClinical SpecialistExton, PAThe ideal candidate will be the go-to expert for device training, therapy education, and enrollment support, ensuring that the trials are conducted with the highest level of clinical integrity. We are looking for a seasoned Registered Respiratory Therapist (RRT) with a strong background in clinical research to join our client's team in a high-impact, mobile role.
Clinical Nurse II Ambulatory Radiation Oncology - Relocation Offered! MedStar HealthClinical Nurse II Ambulatory Radiation Oncology - Relocation Offered!Bel Air, MD$35.68–$64.71 / hourIndividualizes patients plan of care focusing on short and long-range goals and effectively uses a variety of teaching resources to meet the learning needs of patients and families. RN - Registered Nurse - State Licensure and/or Compact State Licensure Current license as a Registered Nurse in the state or jurisdiction of the facility seeking employment Upon Hire required and.
Manager, Pre‑Clinical & Clinical Compliance Johnson & JohnsonManager, Pre‑Clinical & Clinical ComplianceWest Chester, MassachusettsIn the role as Clinical and Pre-Clinical QA Compliance Manager, GCP Quality activities include GCP Clinical and GLP Preclinical audits will include the following: Preparation prior to the audit, connecting with the clinical research team identified and providing advanced notice including securing availability to conduct the audit. For the DePuy Synthes organization, the Clinical and Pre-Clinical QA Compliance Manager main job responsibilities include conducting internal and external GCP Clinical Quality Assurance (QA) audits which include system, program and clinical site investigator sites as well as GLP Preclinical Quality Assurance Supplier Audits.
Manager, Pre‑Clinical & Clinical Compliance 6149-DePuy Synthes Products Legal EntityManager, Pre‑Clinical & Clinical ComplianceWest Chester, MassachusettsIn the role as Clinical and Pre-Clinical QA Compliance Manager, GCP Quality activities include GCP Clinical and GLP Preclinical audits will include the following: Preparation prior to the audit, connecting with the clinical research team identified and providing advanced notice including securing availability to conduct the audit. For the DePuy Synthes organization, the Clinical and Pre-Clinical QA Compliance Manager main job responsibilities include conducting internal and external GCP Clinical Quality Assurance (QA) audits which include system, program and clinical site investigator sites as well as GLP Preclinical Quality Assurance Supplier Audits.
Clinical Research Coord II Main Line Health SystemClinical Research Coord IIWynnewood, PA$50,793.60–$78,707.20 / yearDaily tasks are conducted on site at the Main Line Health Hospitals and may include the oversight and coordination of a variety of clinical studies, executing study procedures as outlined by the study protocol (and related documents). Just as each of our patients requires a personalized care plan, each of our employees, physicians, and volunteers, bring distinctive talents to Main Line Health.
Clinical Trials Manager Nemours FoundationClinical Trials ManagerWilmington, DECollaborating with Research partners across multiple Nemours sites and Non-Nemours sites this leadership role will work in conjunction with the enterprise coalition for the Nemours Center for Cancer and Blood Disorders (NCCBD). The incumbent supervises and coordinates the responsibilities of research nurses and staff conducting studies and oversees the management of all clinical research projects conducted at Nemours Children's Hospital- Delaware.
Director, Clinical Research Christiana Care Health SystemDirector, Clinical ResearchWilmington, DE$121,180.80–$193,897.60 / yearServes as the Research Institutes liaison with ChristianaCare's Center for Strategic Information Management (CSIM) and responsible for ensuring the Research Institutes data processes, procedures, and permissions are met pre and post EPIC implementation. PRINCIPAL DUTIES AND RESPONSIBILITIES: Responsible for oversight of the Research Institutes portfolio of research projects and related programs ensuring that all research is scientifically rigorous, clinically relevant, ethically sound and meet all institutional, state and federal rules, policies, and regulations.
Clinical Research Coordinator NemoursClinical Research CoordinatorWilmington, DEFull timeParticipates in the design and completion of study protocols; including but not limited to regulatory support and maintenance, the conduct of parental permission/assent process for assigned studies; enrolls study participants; schedules study visits with study participants in accordance with study protocols; develops strategies to assure compliance of study participants with protocol requirements. This position will also support projects and assumes responsibility for the day-to-day operation of program activities, including the regulatory functions, project management, administrative tasks, study conduct, chart review, study enrollment, basic data analysis, RedCap, interpretation of results and reporting of research studies and experiments.
Clinical Research Coordinator II- Orthopedics Nemours FoundationClinical Research Coordinator II- OrthopedicsWilmington, DEThe Clinical Research Coordinator II coordinates, implements and completes clinical research studies and/or clinical trials in the Orthopedics Department at Nemours Children's Hospital Delaware by assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent/consent forms, educating parents/participants, scheduling and conducting study procedures, collecting and recording study data, maintaining detailed study records, interfacing with study sponsors, participation in sponsor study monitoring visits, prepare for and participate in internal and external research audits, maintain various research databases. Coordinates IRB submissions for assigned studies, maintains regulatory documents during conduct of study; develops and utilizes study participant and family teaching tools for study purposes; interfaces with representatives of sponsoring agencies.
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 Technologist II- Biobank Nemours FoundationClinical Research Technologist II- BiobankWilmington, DEEssential Functions: Responsible for processing various biological specimens (blood and body fluid, tissue, bone marrow, etc.) and utilizing databases for specimen tracking and storage, following laboratory protocols and SOP's. This individual will conduct routine specimen processing and shipping for both internally and externally funded projects of interest to the laboratory, including plasma/serum processing, mononuclear cell extraction, tissue culture, specimen data entry, and accessioning.
Clinical Trial Manager Ocugen IncClinical Trial ManagerMalvern, PAThis includes leading the cross-functional study team, managing vendor and site performance, maintaining budget and timelines, and ensuring high-quality data and regulatory compliance. Serve as the primary point of contact for study vendors (e.g., CROs, central labs, IRT, eCOA) and oversee vendor selection, scope development, contracting, and performance management.
Senior Clinical Research Associate Alexion Pharmaceuticals IncSenior Clinical Research AssociateWilmington, DECRA works in close collaboration with (Project Management Clinical Operations (PMCO), Study Start-Up (SSU) manager, Clinical Study Assistant (CSA) and other CRAs in Country Operations Management (COM) to ensure that study commitments are achieved in a timely and efficient manner in the country level. CRA is responsible for the selection, initiation, monitoring and closure of assigned sites in clinical studies, in compliance with Alexion Procedural Documents, international guidelines such as ICH-GCP, and relevant local regulations and that the sites deliver according to their respective commitment in the individual studies.
Senior Clinical Trial Manager Ocugen IncSenior Clinical Trial ManagerMalvern, PACTM leads complex or high-priority studies with minimal supervision, drives study start-up activities, and maintains strong engagement with investigators and study physicians. This role requires a hands-on, highly organized individual who is comfortable operating in a fast-changing, resource-constrained environment and who can drive execution through vendors, CROs, and internal teams.
Clinical Research Coordinator Nemours FoundationClinical Research CoordinatorWilmington, DEParticipates in the design and completion of study protocols; including but not limited to regulatory support and maintenance, the conduct of parental permission/assent process for assigned studies; enrolls study participants; schedules study visits with study participants in accordance with study protocols; develops strategies to assure compliance of study participants with protocol requirements. This position will also support projects and assumes responsibility for the day-to-day operation of program activities, including the regulatory functions, project management, administrative tasks, study conduct, chart review, study enrollment, basic data analysis, RedCap, interpretation of results and reporting of research studies and experiments.
NewSenior Clinical Trial Manager Incyte CorpSenior Clinical Trial ManagerWilmington, DEJob Summary Primary Function The Sr Clinical Trial Manager provides input to the overall operational trials implementation manages trials timelines budget feasibility country identification and sites selection enhanced patient recruitment functions as the primary liaison for internal stakeholders and vendors leads multidisciplinary departments initiatives and provides support for process changes to increase efficiency in study executions. Through the discovery development and commercialization of proprietary therapeutics Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology Oncology and Inflammation and Autoimmunity Headquartered in Wilmington Delaware Incyte has operations in North America Europe and Asia.
Clinical Dietitian Coordinator Main Line Health SystemClinical Dietitian CoordinatorMalvern, PA$34.96–$54.16 / hourIn addition to clinical responsibilities, the Lead Dietitian devotes approximately 20% of their role to providing administrative and staff support to Clinical Nutrition Manager (CNM), contributing to departmental operations, staff coordination, and quality initiatives. The Lead Dietician functions as an integral member of the multidisciplinary healthcare team, collaborating to develop, coordinate, implement, and assess individualized nutrition care plans that support optimal patient outcomes.
NewDirector, Clinical Operations Asset Lead GSK, Plc.Director, Clinical Operations Asset LeadUpper Providence, PA$189,750–$316,250 / yearWorking in close partnership with clinical, biostatistics, and functional experts, the COAL drives informed decision‑making, provides strategic leadership to Study Delivery Teams, and ensures high‑quality, on‑time delivery-while retaining full accountability for overall asset outcomes. Analytical Thinking, Business Acumen, Change Management, Clinical Research, Clinical Trial Designs, Communication, Decision Making, Fostering Collaboration, Influencing Without Authority, Leadership, Matrix Leadership, Mentorship, People Management, Risk Management, Strategic Thinking.
Clinical Research Coordinator RN Registered Nurse (Full Time/Days) Penn MedicineClinical Research Coordinator RN Registered Nurse (Full Time/Days)Lancaster, PAQualified individuals must have the ability with or without reasonable accommodation to perform the following duties: Plans and coordinates assigned research studies, serves as principle liaison for the project, interfaces with research subjects and collects research data, oversees administrative support, develops appropriate tools needed to conduct the research, and maintains record keeping systems and procedures. Functions as a resource for physicians, other health care providers, and ancillary support staff regarding care of the research participant as it relates to any given clinical research protocol; conducts staff in-services as appropriate.
Senior Clinical Data Manager Ocugen IncSenior Clinical Data ManagerMalvern, PAThis individual will lead data management efforts, oversee quality data collection and management processes, and contribute to critical aspects of clinical trial data handling, including database design, CRF development, data monitoring, and validation for clinical development programs and marketed products. In addition to technical responsibilities, the Senior Clinical Data Manager will provide leadership to junior data management staff and work collaboratively across functional teams, ensuring high-quality and timely deliverables.