NewService Line Coordinator Moorestown Surgery Center Cooper University Health CareService Line Coordinator Moorestown Surgery CenterMoorestown, NJAssumes responsibility and accountability for the coordination and implementation of patient care services within the Operating Room at the direction of the Clinical Director and Clinical Director: Coordinates the daily activities of the assigned specialty service(s) in the Operating Room. Successful completion of an appropriate training program for Surgical Technology in the Army, Navy, Air Force, Marine Corps, or Coast Guard of the United States or in the United Dates Public Health Service Commissioned Corps; OR.
Admin Coordinator PRN CNI Cooper University Health CareAdmin Coordinator PRN CNICamden, NJThis position supports the Cooper Neurological Institute (CNI) and requires the incumbent to register and schedule patients for outpatient office appointments, procedures, and/or surgeries and assists with tasks related to patient care and appointments e.g. This position works in collaboration with all CNI team members, as well as other Cooper departments, including but not limited to, nursing, health care access, patient access center, lab testing, radiology, and OR.
Facility Dog Program Coordinator Children's Hospital of PhiladelphiaFacility Dog Program CoordinatorPhiladelphia, PAClinical Excellence: Provides expert child life services to patients and family members, including developmentally appropriate therapeutic activities, education, procedural preparation, coping facilitation, and support as it relates to their illness and medical treatment with facility dog, as appropriate. Assess, develop, and/or deliver educational trainings for healthcare professionals across the enterprise for matters including but not limited to evidence-based practices related to animal-assisted therapies, developmental care, language and preparation, coping facilitation and pain management techniques.
Senior Treatment Coordinator - Fletcher House Volunteers of America Delaware ValleySenior Treatment Coordinator - Fletcher HouseCamden, New JerseySCOPE OF DUTIES: Ensure the provision of direct services to all clients entering the program: •Quality assurance of initial assessments and its relationship to the development of service plans for all residents. Responsible for the coordination of providing direct supervision to case management staff and ensuring clients receive appropriate services based on assessed need.
Senior Treatment Coordinator -FVPP Volunteers of America Delaware ValleySenior Treatment Coordinator -FVPPCamden, New JerseySCOPE OF DUTIES: Ensure the provision of direct services to all clients entering the program: •Quality assurance of initial assessments and its relationship to the development of service plans for all residents. Responsible for the coordination of providing direct supervision to case management staff and ensuring clients receive appropriate services based on assessed need.
Clinical Trial Manager Impulse Dynamics Germany GmbHClinical Trial ManagerMarlton, NJ$95,000–$115,000 / yearFor Associate CTM: Minimum of 2 years of progressive experience in clinical operations, clinical trial management, or project management within the pharmaceutical, biotechnology, medical device, or contract research organization (CRO) industries. Lead study startup processes, including but not limited to conduct of the clinical trial Investigator meeting together with clinical and medical leadership, site selection, and finalization of site clinical trial site agreements and budgets.
Clinical Appeals Coord Blue Cross and Blue Shield AssociationClinical Appeals CoordPhiladelphia, PAExperience supporting external review, independent review organization cases, peer review coordination, expedited appeals, complex medical necessity appeals, pharmacy appeals, behavioral health appeals, or benefit appeals preferred. This role applies clinical nursing judgment, utilization management knowledge, benefit interpretation, medical policy, and evidence-based review criteria to ensure appeals are reviewed accurately, thoroughly, and within applicable regulatory, accreditation, and contractual timeframes.
Global Director, Clinical Project Management SystimmuneGlobal Director, Clinical Project ManagementPrinceton, NJ$180,000–$230,000 / yearIt specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development.
NewAssociate Director - Clinical Trial Management Business Partnering & Category Strategy Teva Pharmaceutical Industries LtdAssociate Director - Clinical Trial Management Business Partnering & Category StrategyWest Chester, PAAdditional benefits include, but are not limited to, Employee Assistance Program, Employee Stock Purchase Plan, Tuition Assistance, Flexible Spending Accounts, Health Savings Account, Life Style Spending Account, Volunteer Time Off, Paid Parental Leave, if eligible, Family Building Benefits, Virtual Physical Therapy, Accident, Critical Illness and Hospital Indemnity Insurances, Identity Theft Protection, Legal Plan, Voluntary Life Insurance and Long Term Disability and more. Reporting to the Director - Clinical Development Business Partnering & Category Strategy, this role is responsible for assigned Clinical Trial Management categories, with primary focus on Full-Service Outsourcing (FSO), Functional Service Provider (FSP), and related clinical operations services.
Senior Director, Clinical Operations Theradex OncologySenior Director, Clinical OperationsPrinceton, New Jersey$180,000–$220,000 / yearFull timeWe're seeking a Senior Director, Clinical Operations to lead Clinical Project Managers and Clinical Research Associates teams, drive strategic decisions, manage departmental budgets while ensuring profitability and compliance. Strategic Planning & Resource Management Optimize resource allocation and proactively identify skill gaps to maximize team effectiveness across multiple trials.
Clinical Development Trial Lead ICON PlcClinical Development Trial LeadBlue Bell, PAThe Clinical Development Trial Lead (CDTL) Associate leads the cross-functional study team in the development and execution of clinical trials and is accountable both regionally and globally to deliver trial(s) with quality, on time, and within scope and budget. The CDTL Associate leverages project management, regional operational knowledge, clinical trial process leadership and expertise, and scientific expertise to drive actions and coordinate efforts to achieve or exceed these trial deliverables.
Senior Manager/Associate Director, Clinical Pharmacology SystimmuneSenior Manager/Associate Director, Clinical PharmacologyPrinceton, NJ$150,000–$200,000 / yearThe ideal candidate will provide expertise in pharmacokinetics, dose optimization, pharmacometrics, and drug interaction assessment, collaborate with cross-functional teams (Clinical, Research, Regulatory, Biometrics, etc.), and manage clinical pharmacology studies, data analysis, and regulatory filings. Take a lead role in preparing and meticulously reviewing clinical pharmacology sections of study protocols, reports, investigators' brochures and regulatory filings (IND’s, BLA’s, etc.), and responds to regulatory inquiries related to clinical pharmacology.
Associate Director, Oncology Clinical Biomarker Asset Lead, Translational Development Bristol Myers SquibbAssociate Director, Oncology Clinical Biomarker Asset Lead, Translational DevelopmentPrinceton, NJ$214,020–$259,344 / yearBased on eligibility*, additional time off for employees may include unlimited paid sick time, up to 2 paid volunteer days per year, summer hours flexibility, leaves of absence for medical, personal, parental, caregiver, bereavement, and military needs and an annual Global Shutdown between Christmas and New Years Day. Key responsibilities of this role are to act as a lead scientist to implement and deliver on biomarker strategies for clinical programs, develop reports and publications on translational data generated to support asset development and contribute to regulatory submissions.
Mental Health Technician Adams ClinicalMental Health TechnicianPhiladelphia, PA$22–$24 / 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.
Temporary Employee - Non-Exempt University of PennsylvaniaTemporary Employee - Non-ExemptPhiladelphia, PA$7.25–$16 / hourThe focus of the GBM TCE is driven by the needs of clinicians and translational scientists and realized through collaborative work with researchers in the Penn School of Medicine, the Penn School of Engineering, and the Center for Personalized Diagnostics. You will learn how to perform data entry in clinical study databases such as REDCap, VELOS Clinical Trial Management System, patient medical charts, and Excel files, and abstracting data from medical records.
NewSite Operations Specialist Science 37Site Operations SpecialistMorrisville, PAWorking cross-functionally, the Site Operations Specialist provides operational support to Site Operations Managers, Logistics Managers, Medical Record Supervisors, Recruitment Operations Managers, Scheduling Logistics Managers, Clinical Project Managers, and Clinical Research Coordinators. Responsible for maintaining key study trackers, including but not limited toStudy Contacts Lists, Study Question and Answer Logs, Site Budgets Log, clinical site contracts tracker, medical record status, and participant trackers.
Grants Manager A/B University of PennsylvaniaGrants Manager A/BPhiladelphia, PA$65,628–$77,330 / yearHandle all pre-award activities for patient oriented clinical trials federal and non-federal including completion of Prospective Reimbursement Analysis (PRA) with Clinical Research Coordinators(CRCs)/PIs, Research Billing Number (RBN) set-up, advance account paperwork if required, invoicing start-up, tracking initial payments, etc. The GM will monitor and enforce compliance with sponsor guidelines and OMB Uniform Guidance, meet with principal investigators to discuss and advise them on financial issues related to their portfolios, maintain salary grids and support with payroll allocations to ensure faculty and staff are paid correctly, and assist in the preparation of effort reports.
Drug Safety Associate I Integrated Resources, IncDrug Safety Associate IHorsham, PennsylvaniaContractorPRINCIPAL RESPONSIBILITIES: Case processing: 95% Definition: The completion of full case information on the database, including quality review to ensure accuracy and completeness Activities Include: May Triage and classify ICSRs for report type, seriousness, causality, expectedness/labeling and reporting; prioritize ICSR according to regulatory requirements Confirmation of Safety Coordinator case registry data Database searches as necessary Completion of remaining case data entry, including narrative or auto-narrative Completion of risk and quality (label, approval, manual coding and quality review steps). Pharmaceutical industry experience is preferredRequired Skills/Abilities Intermediate Information Technology Skills Data entry experience desired Accountability for delivery of results Decision making skills Problem solving skills Proactive approach/uses own initiative Manages owe work, able to prioritize, plan and organize work assignments and work under strict timelines Ability to follow guidelines, working practices etc.
Associate Director D University of PennsylvaniaAssociate Director DPA$92,592–$96,000 / yearThe Associate Director is a non-attorney (BA required, JD or MA preferred) contracting professional who independently negotiates and executes a portfolio of moderately complex clinical research agreements and serves as the complexity bridge between Senior Contract Administrators and attorney-level contracting staff. 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.
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.