Clinical Specialist/Licensed Clinical Specialist - PACT Program Cumberland County Guidance CenterClinical Specialist/Licensed Clinical Specialist - PACT ProgramBridgeton, NJFull timeKey ResponsibilitiesProvide individual and group counseling servicesComplete psychosocial assessments and crisis evaluationsDevelop and implement individualized treatment and recovery plansCoordinate care with medical, clinical, and community providersSupport medication monitoring, treatment adherence, and wellness planningEngage family members and natural supports in the recovery processConnect individuals with housing, benefits, healthcare, and community resourcesAssist clients in developing independent living and community integration skillsParticipate in community-based interventions and transportation as neededMaintain timely and accurate clinical documentationParticipate in the program's on-call rotation scheduleRequired QualificationsClinical Specialist (Non-Licensed)Master's Degree in Social Work, Psychology, Counseling, or a related Human Services fieldMinimum two years of post-bachelor's experience working with individuals living with severe and persistent mental illnessKnowledge of behavioral health systems and community resourcesValid New Jersey driver's license with acceptable driving historyLicensed Clinical SpecialistMaster's Degree in Social Work, Psychology, Counseling, or a related Human Services fieldCurrent New Jersey LSW or LAC licenseMinimum two years of post-bachelor's mental health experienceExperience working with individuals living with severe and persistent mental illnessKnowledge of behavioral health systems and community resourcesValid New Jersey driver's license with acceptable driving historyPreferred QualificationsLCSW, LPC, or other advanced clinical licensureExperience providing individual and group therapyCommunity mental health experienceCrisis intervention experienceExperience working within PACT programsExperience collaborating within multidisciplinary treatment teamsBilingual English/SpanishReady to Make a Lasting Impact? Compensation Based on Licensure:Clinical Specialist (Non-Licensed Master's Level): $45,000Licensed Clinical Specialist (LSW/LAC): $55,000Comprehensive Benefits PackageMedical InsuranceDental InsuranceVision InsuranceLife InsurancePaid Time Off (PTO)Employee DiscountsProfessional Development OpportunitiesClinical Training and Licensure SupportWhat You'll DoAs a Clinical Specialist, you'll work closely with psychiatrists, nurses, case managers, peer specialists, and community providers to support individuals receiving PACT services.
Clinical Research Coordinator I CenExelClinical Research Coordinator IMarlton, New JerseyResponsible for assisting with coordinating clinical trials with the strictest adherence to ICH (International Conference on Harmonization), GCP (Good Clinical Practices), protocol, and company guidelines, regulations, and policies. We focus on quality people, teamwork, and highly experienced clinical research managers with a history of success.
Adjunct Faculty, Early Childhood Education Clinical Field Supervisors - Department of Early Childhood, Elementary Education & Clinical Foundations Rowan UniversityAdjunct Faculty, Early Childhood Education Clinical Field Supervisors - Department of Early Childhood, Elementary Education & Clinical FoundationsGlassboro, NJIn compliance with The State of New Jersey''''s Pay Transparency Act, and in accordance with the current MOA, Rowan University adjuncts are provided with a minimum of $2,225 per credit for all courses taught, with a maximum teaching load of 8 credits per semester and 12 credits in an academic year. The fastest-growing public research institution in the Northeast and among the country's top 10 fastest-growing, Rowan offers a thriving multidisciplinary environment with a strong emphasis on practical research in health care, engineering, science and business, while ensuring excellence in undergraduate education.
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.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedNJ$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.
NewClinical Research Technologist Nemours FoundationClinical Research TechnologistWilmington, DEResponsibilities include: Receives biospecimens from the LHC collection sites into the ALA-ACRC biorepository housed at Nemours Biobank and Molecular Analysis Program (BMAP), which includes tracking incoming shipments, accepting shipments, cataloging shipment biospecimens, completing paperwork and computer entry related to acquisition. This individual will manage receipt and storage of biospecimens from the (LHC) American Lung Association Airways Clinical Research Center network (ALA-ACRC) sites and other ALA-ACRC studies as required.
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 Supplies Manager (Remote Based) Syneos HealthClinical Trial Supplies Manager (Remote Based)DelawareRemoteKnowledge of IRT system set-up, functionality, and proficiency with excel modeling - support IRT user acceptance testing, develops IRT supply strategy, and oversees ongoing supply activities in the system. Over the past 5 years, we have worked with 94% of all Novel FDA Approved Drugs, 95% of EMA Authorized Products and over 200 Studies across 73,000 Sites and 675,000+ Trial patients.
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.
Clinical Research Associate - Full-Service Syneos Health IncClinical Research Associate - Full-ServiceDETogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health IncExperienced Clinical Research Associate - Sponsor DedicatedDETogether we share insights, use the latest technologies and apply advanced business practices to speed our customers' delivery of important therapies to patients. Selecting us as an employer secures a career in which you're guaranteed to: Collaborate with passionate problem solvers Partner with the most diverse team of experts in the industry.
Clinical Sales Specialist, Electrophysiology - LAAO (Philadelphia/Wilmington) Abbott LaboratoriesClinical Sales Specialist, Electrophysiology - LAAO (Philadelphia/Wilmington)Wilmington, DE$61,300–$122,700 / yearIn this role, the Clinical Specialist with train interventional cardiologists, catheter lab staff and ancillary personnel on the use of Structural Heart products and provide technical support to physicians during procedures. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines.
Clinical Trial Supply (CTS) Study Manager CSL PlasmaClinical Trial Supply (CTS) Study ManagerEmea, DelawareWe 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.
NewClinical Research Assistant Nemours FoundationClinical Research AssistantWilmington, DEThe job includes but is not limited to: screening patients for study eligibility, scheduling research visits/follow up, tracking/auditing consent forms and study related documents, preparation for both internal and external audits, collecting data and submitting to appropriate organizations, processing/packaging of lab specimens, maintaining inventory of research supplies, creating electronic research charts, scheduling site monitor visits and meeting rooms as needed and assisting in the implementation of new laboratory protocols and processes. The Clinical Research Assistant will be required to complete Human Subjects Protection (HSP) training, CITI training (including Good Clinical Practice (GCP), as well as become a member of the Children's Oncology Group (COG) research base.
Clinical Manager University Health Services IncClinical ManagerCHESTER, PAOperating acute care hospitals, behavioral health facilities, outpatient facilities and ambulatory care access points, an insurance offering, a physician network and various related services located all over the U.S. States, Washington, D.C., Puerto Rico and the United Kingdom. The Clinical Manager primary responsibilities include coordinating all clinical services occuring during the evening or weekend shift, supervision of clinical staff working on shift as well as providing crisis intervention and completion of documentation as assigned.
Director of Clinical Management & Intake Enlyte Group LLCDirector of Clinical Management & Intakeegg harbor, NJ$133,100–$150,000 / yearThe Director drives operational excellence, champions AI and automation initiatives, participates in business development efforts, and partners with claims leadership, medical providers, clients, and internal stakeholders to ensure high-quality, cost-effective clinical management services and positive outcomes for injured workers. This leader oversees teams of Nurse Case Managers, Clinical Support Coordinators, Intake Representatives, and administrative support staff, and holds ownership of departmental budgets, workforce planning, succession planning, and key performance metrics including referral turnaround time, clinical outcomes, network utilization, and client satisfaction.
Bilingual (Spanish/English) Clinical Research Coordinator Nemours FoundationBilingual (Spanish/English) Clinical Research CoordinatorWilmington, DEEssential CRC duties include coordinating IRB submissions, maintaining an up-to-date study regulatory binder, reviewing documentation for study recruitment and completion, monitoring participant status in relevant databases, organizing participant payments, maintaining regular contact with research coordinators across the trial sites, attending meetings with the Principal Investigator and Co-Investigators for the study, and helping to ensure that the study runs smoothly by problem-solving any issues with screening, recruitment, or data collection as they arise. Research projects span a variety of medical conditions (e.g., cancer, sickle cell disease, diabetes, pain, asthma, food allergy, disordered eating) and other health-related challenges (transition from pediatric to adult healthcare, behavioral interventions to improve coping with disease and treatment demands).
Manager of Clinical Appeals and Grievances HealthfirstManager of Clinical Appeals and GrievancesDE$103,400–$149,430 / yearProvides guidance in the preparation of case preparation for Medical Director Review ensuring that all pertinent information (i.e. case summary, contract information, internal and external responses, diagnosis, and CPT codes and descriptions) has been obtained during investigation and is presented as part of the case. If you have a disability under the Americans with Disability Act or a similar law and want a reasonable accommodation to assist with your job search or application for employment, please contact us by sending an email to careers@Healthfirst.org or calling 212-519-1798.
Clinical Director Boca Recovery CenterClinical DirectorGalloway, NJAs the Clinical Director at Boca Recovery Center, you will oversee and lead our clinical staff, ensuring the delivery of high-quality, evidence-based treatment for clients with substance use disorders and co-occurring mental health conditions. With facilities in Florida, New Jersey, Indiana, and Massachusetts, we implement evidence-based practices within a supportive environment, dedicated to fostering sustainable recovery.
Clinical Affairs Scientist Agilent Technologies IncClinical Affairs ScientistDE$105,280–$197,400 / yearThe candidate will work directly with pharmaceutical partners, R&D scientists, Clinical Trial Managers/ Clinical Research Associates, Quality Assurance, and Regulatory Affairs to assure compliance with internal and external requirements. We are searching for an experienced Clinical Affairs Scientist (CAS) to work within the medical diagnostic field as a key member of the Organization of Chief Medical Officer (OCMO) Global Clinical Affairs team.