Clinical Product Data Steward Dale Workforce SolutionsClinical Product Data StewardWayne, PARemoteThe strongest candidates will have hands-on experience maintaining clinical product master data for a pharmaceutical or biotech organization, particularly data associated with molecules, compounds, formulations, clinical products, and their evolution throughout the development lifecycle. These individuals will be responsible for establishing and maintaining the structures, hierarchies, naming conventions, and relationships associated with pharmaceutical products as they progress through the clinical development lifecycle.
Associate Director, Clinical Study Start-Up Summit TherapeuticsAssociate Director, Clinical Study Start-UpPrinceton, New Jersey$174,000–$204,000 / yearHARMONi: Phase 3 clinical study which was intended to evaluate ivonescimab combined with chemotherapy compared to placebo plus chemotherapy in patients with EGFR-mutated, locally advanced or metastatic non-squamous NSCLC who were previously treated with a 3rd generation EGFR TKI. HARMONi-3: Phase 3 clinical study which is intended to evaluate ivonescimab combined with chemotherapy compared to pembrolizumab combined with chemotherapy in patients with first-line metastatic NSCLC.
NewClinical Business Development Executive (Midwest Territory) PCI Pharma ServicesClinical Business Development Executive (Midwest Territory)Philadelphia, PAUpdate database information with new business opportunities, client data, and communications of all forms Maintain and expand working relationships with existing clients and internal teams to expand sales and ensure client satisfaction. The Clinical Business Development Executive will grow profitable sales with existing customers and develop business with prospective new customers for the Midwest territory.
Clinical Business Development Executive (Midwest Territory) PCI ServicesClinical Business Development Executive (Midwest Territory)Philadelphia, PAUpdate database information with new business opportunities, client data, and communications of all forms Maintain and expand working relationships with existing clients and internal teams to expand sales and ensure client satisfaction. The Clinical Business Development Executive will grow profitable sales with existing customers and develop business with prospective new customers for the Midwest territory.
Executive Director, Clinical Development Physician (Autoimmune) Immunocore Holdings PlcExecutive Director, Clinical Development Physician (Autoimmune)Radnor, PAVacancy NameExecutive Director, Clinical Development Physician (Autoimmune) Vacancy NoVN866 Employment TypeFull Time Location of roleGaithersburg, MD, Radnor, PA, Oxford, UK DepartmentClinical Development Key ResponsibilitiesThe Executive Director, Early-Stage Clinical Development, Autoimmune will drive assigned autoimmune programs from pre-clinical stages to proof of concept. As a key in-house autoimmune disease expert for R&D, this role requires strong strategic leadership, advisory skills, and close collaboration with cross-functional teams whilst providing oversight, guidance, and mentorship to junior physicians working in early-stage clinical trials.
SDTM, Clinical SAS Programmer Karwell TechnologiesSDTM, Clinical SAS ProgrammerNorth Wales, PAJob Description: Looking for SDTM experts having in-depth knowledge of SAS programming(macro's). Create advanced SAS macros, templates, and utilities for efficient data processing.
Clinical Laboratory Technologist - Microbiology LabCorpClinical Laboratory Technologist - MicrobiologyRaritan, NJ$28.50–$39.09 / hourAs we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes.
Clinical Laboratory Technologist Trainee - Toxicology LabCorpClinical Laboratory Technologist Trainee - ToxicologyRaritan, NJ$25.19–$39.09 / hourAs we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes.
NewClinical Laboratory Technologist Trainee - Microbiology LabCorpClinical Laboratory Technologist Trainee - MicrobiologyRaritan, NJ$28.50–$39.09 / hourAs we shape the future of healthcare, we are leveraging advanced technologies, intelligent digital solutions and data-driven innovation across our operations to enhance how work gets done and deliver greater value to customers and patients. Labcorp is a global leader in laboratory services, providing the insights and answers that help healthcare providers, patients, researchers, pharmaceutical companies and health systems make confident decisions and improve outcomes.
Clinical Education Specialist Essity Aktiebolag (publ)Clinical Education SpecialistPhiladelphia, PARemoteCollaborative and Caring Culture | Empowerment & Engaged People | Work with Impact and A Powerful Purpose | Individual Learning & Career Growth | Health & Safety Priority | Sustainable Value Together| Innovation| Sustainable Working Life | Total Reward. The Clinical Resource Manager will be responsible for developing/delivering educational services and value-added resources to support both internal and external customers.
Associate Director, Clinical Data Management Genmab ASAssociate Director, Clinical Data ManagementPrinceton, NJFor 25 years, its hard-working, innovative and collaborative team has invented next-generation antibody technology platforms and harnessed translational, quantitative and data sciences, resulting in a proprietary pipeline including bispecific T-cell engagers, antibody-drug conjugates, next-generation immune checkpoint modulators and effector function-enhanced antibodies. As Associate Director, Data Management, the employee may be involved in: General/Trial specific: Give input to the clinical development plans through the Development Operations representatives of the CDT ensuring that data management input/knowledge that could impact the setup and conduct of trials is proactively considered and discussed upon development of the operational strategy of the trials.
Clinical Case Manager III for Adult OP Services Belmont Behavioral Health SystemClinical Case Manager III for Adult OP ServicesPhiladelphia, PennsylvaniaLead the flow of information between levels of care by collaborating with the admissions department, clinical and financial departments, and the patient and their family/guardian throughout program to provide a smooth transition at discharge. Perform concurrent review with network providers; monitor medical record documentation using knowledge of established guidelines to promote compliance and further ensure quality for retrospective review by external review entities.
NewClinical Nurse Educator (per diem) - East Coast IQVIA Holdings IncClinical Nurse Educator (per diem) - East CoastPhiladelphia, PA$40–$45 / hourIndividuals are typically required to have completed/up to date: Measles, Mumps & Rubella vaccine, Varicella (chicken pox) vaccine, Negative Tuberculosis (TB) Test, Tetanus, Diphtheria & Pertussis (Tdap) vaccine, Hepatitis B vaccine, Influenza vaccine (seasonal), and COVID-19 vaccine primary series (heavily enforced by most facilities, some require booster(s)). Our MedTech Clinical Nurse Educators experience a unique opportunity to employ their clinical nursing expertise in a new way outside patient care, while continuing to collaborate with healthcare professionals and advocate for the well-being of patients through medical device technology.
NewClinical Medical Assistant – Patient Assessments The IMA GroupClinical Medical Assistant – Patient AssessmentsPhiladelphia, PennsylvaniaOur Payer Services Division meets the evaluation and screening needs of Carriers, TPAs, Public Entities and Employers and includes behavioral health and physical medicine specialty services, working with a wide range of organizations within the workers' compensation, disability, liability, and auto markets. Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.
Clinical Program Director (RN Required) HealogicsClinical Program Director (RN Required)Darby, PennsylvaniaWorks directly with the hospital and Healogics marketing departments to ensure that the wound care program has established strategic marketing plans and works with the same group and the hospital physician liaison to plan, coordinate, and execute activities directed toward increasing patient referrals to the Wound Care Center (WCC)®(s). As needed, serves as case manager to a group of wound care patients, to include specific assessments and direct patient care according to protocols and procedures, clinical competence in procedural skills, treatments, and patient/caregiver education related to wound care management.
NewClinic Manager/LICENSED Clinical Supervisor -Outpatient Mental Health Ellie Mental HealthClinic Manager/LICENSED Clinical Supervisor -Outpatient Mental HealthNorth Wales, Pennsylvania$75,000–$100,000 / yearEssential Duties: · Maintain billable hours expectations · Participate in the Ellie clinic manager meetings which includes reviewing clinic KPIs and clinic accounts receivable (client & insurance) · Triage clinic staff’s administrative questions and concerns by connecting them to appropriate tools and resources · Troubleshoot issues with Clinic Director and Biller in relation to systems such as Valant, Teams, Outlook, credentialing and Billing · Collaborate with clinic director to support clinic in positive culture building (celebrations, anniversaries, community activities/events, team building activities, etc.) · Monitor clinic capacity and practice patterns in support of the clinic director in hiring to meet FTE staffing requirements (office space and client waitlist) · Partner with clinic director to monitor clinic staffing (Caseloads, hiring, office space and waitlists) · Increase avg appointments per patient by working on strategies with staff · Coordinate with clinic director to support the hiring process; this includes screening, interviewing, and onboarding processes · Coordinate office supply orders for clinic (ordering and monitoring) · Co-facilitate clinic meetings and facilitate consultation groups, supervision and including documentation via Valant · Collaborate with clinic director to maintain organizational policies and procedures · Audit documentation for clinic in Valant to ensure compliance and compliance. · Serve as back-up for CD when they are out of the office · Additional duties as assigned Qualifications: · Master’s degree or higher in a mental health discipline · Active clinical license in state of PA (LCSW, LPC and LMFT) for a minimum of 4.5 years and experience as a clinical supervisor.
Vice President, Clinical Development, Tonlamarsen (TLA) KardiganVice President, Clinical Development, Tonlamarsen (TLA)Princeton, New JerseyThe Vice President owns the Clinical Development Plan, leads the design of the clinical protocol, provides matrix leadership for the cross-functional program team, direct management of the Clinical Development Medical Director(s) and Clinical Scientist(s), and brings deep biotech clinical development experience to a fast-moving late-stage program. Proven leadership in managing a cross-functional, matrixed team to develop and implement a program-wide clinical development plan, including scenario planning, assessment of clinical trial design scenarios for commercial/medical launch strategy and therapeutic adoption, partnership with Biometrics on evidence generation strategy, and partnership with Clinical Operations on operational strategy.
BCBA Clinical Supervisor CORA Services IncBCBA Clinical SupervisorPhiladelphia, PAFull timeMinimum two years of full-time clinical professional experience working with students with Autism and/or Emotional Disturbance, developing Functional Behavioral Assessments and behavior plans, and providing training on behavioral interventions, classroom management, and intervention techniques (e.g., Positive Behavior Intervention Supports, Discrete Trial Training, Picture Exchange Communication System, Social Skills training, and Communication Training). Responsibilities include providing Behavior Analytic services to assigned caseload while supervising specific clinical staff (staff onboarding, quality service delivery, and utilization of services), including managing ongoing staff BACB competency assessments (training & supervision).
Clinical Supervisor ElwynClinical SupervisorElwyn, PennsylvaniaFull timeDIRECT REPORTS: Therapists, Case Managers CONTACTS: Elwyn staff, individuals, families/ guardian/ support system of clientele, visitors, funding sources/agencies/social service agencies, community mental health centers and hospitals, advocacy groups, employers, health maintenance organizations, community resource liaisons, interns EDUCATION/EXPERIENCE/SKILLS REQUIREMENTS: Master's degree in clinical psychology, social work, or related field. Oversees programmatic and administrative issues, including client admissions, service modifications, program planning, and regulations to ensure program compliance and quality of client care; works collaboratively with managed care organizations (MCOs) and county liaisons and provides support to team with outside providers if the need arises regarding continuity of individual's care.
Business Analyst, Clinical Systems SuvodaBusiness Analyst, Clinical SystemsConshohocken, PAResponsibilities: Work on a cross-functional project team responsible for the delivery of Interactive Response Technology (IRT) for randomization and drug supply management; Design the IRT solution to meet the study requirements based on the clinical protocol, the Suvoda proposal/executed work order, and discussions with the client; Consult with clients to best understand their business requirements and act as a trusted advisor for translating these requirements into Suvoda's software; Accurately and completely document all requirements in the specification template(s); Lead the internal team review of the draft specifications; main point of contact for the internal team for all IRT design related questions throughout the build process; Lead the client review of the IRT specifications and supporting documents, making any required updates and obtaining both client and internal approval by the agreed upon milestone date; Responsible for the UAT plan, test scripts, and coordinate all required data setup for client UAT; Primary point of contact for design questions (internally and externally) during the system build process; Lead client UAT of the IRT system, tracking any required fixes or updates; work with the project manager to determine timelines for any system updates required; Support any re-design of the IRT system or implementation of new features in an IRT system during the maintenance period • Identify and assist with the implementation of process improvements for the services department; Assist the product team with the design and development of new features by providing feedback based on client requests and project experience. Travel to client sites to attend meetings and conduct user training sessions; Assist the customer care team with providing support to system users (as required) via the telephone and email; Assist with the training of new staff members on the Suvoda product and processes; Perform continuous risk assessments throughout the project lifecycle to identify new risks and update mitigation strategies accordingly; Perform other related duties as required; Requirements: 2-3 years of experience in a similar role; 1 year of experience in IRT or related field preferred; Bachelor's degree or equivalent experience required; Interpersonal and communication skills; Time management and organizational skills; Analytical and systematic thinking ability; Creative problem solving; Ability to understand technical details and translate them to non-technical users; Attention to detail; Demonstrated strong consultative skills.