Open-Rank Professor of Practice, Non-Tenure Track, Clinical Mental Health Counseling Saint Joseph's UniversityOpen-Rank Professor of Practice, Non-Tenure Track, Clinical Mental Health CounselingPA$68,000–$72,000 / yearNotice to Out of State Applicants: Saint Joseph's University may only consider applicants from Pennsylvania, New Jersey, New York (not including New York City zip codes), and Delaware (Delaware residents for positions with over 50% work time on a SJU campus). This is an exciting opportunity for someone who is strongly interested in building and fostering community connections; active involvement in CACREP accreditation; service to the university, department, and program; and committed to counselor identity and academic quality in the preparation of counselors.
Clinical Rescue Nurse Coordinator, Per Diem - Resuscitation and ECMO Program (6a-6p or 6p-6a) Temple HealthClinical Rescue Nurse Coordinator, Per Diem - Resuscitation and ECMO Program (6a-6p or 6p-6a)Philadelphia, 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. As the chief clinical training site for the Lewis Katz School of Medicine at Temple University, the hospital provides a dynamic environment for high-quality care, teaching, and cutting edge research.
ABA Clinical Associate / Lindens Children's Program /2nd shift BancroftABA Clinical Associate / Lindens Children's Program /2nd shiftMount Laurel, New JerseyFull timeRequirements: High School diploma or GED, valid Driver’s License, six months related work experience, or, a Bachelor’s degree in Psychology, Social Work, or a related field or currently enrolled in a related college program are required. Outstanding Benefits: We offer competitive salaries, tuition assistance up to $5,250 each year, tuition loan repayment assistance, discounted tuition at local colleges and universities, retirement savings programs, generous paid time off, medical and dental insurance, and more.
Clinical Director/Hygienist: Tamaqua, PA Temple UniversityClinical Director/Hygienist: Tamaqua, PAPhiladelphia, Pennsylvania$80,000–$90,000Other responsibilities will include working closely with the Faculty Director, other providers and staff to resolve any issues regarding patient treatment plans, scheduling, or anything involving clinical/office operations; managing inventory, equipment, and supplies; reviewing patient flow and all steps in the care process, and ensuring that patients receive quality care in a timely and respectful manner; community engagement and school-based oral health program development to expand access for underserved populations; and public speaking, advocacy, and program leadership focused on improving rural oral health outcomes. Once clinical operations begin, the Clinical Director will be responsible for systems management, including scheduling optimization, tele-dentistry implementation, and process improvement initiatives as well as strategic planning and service expansion to meet high patient demand while maintaining quality of care.
Clinical Veterinarian (Onsite - King Of Prussia, PA) Pharmavise CorporationClinical Veterinarian (Onsite - King Of Prussia, PA)King Of Prussia, PennsylvaniaThis role provides veterinary oversight across research programs, leads and supports a team of veterinary technicians and animal care staff, and serves as a key scientific and welfare advisor to study directors. The position requires hands-on clinical expertise, strong leadership capability, and the ability to operate effectively in a fast-paced, regulated laboratory environment.
Coordinator, Clinical Analysis & Appeals Temple HealthCoordinator, Clinical Analysis & AppealsPhiladelphia, 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. As the chief clinical training site for the Lewis Katz School of Medicine at Temple University, the hospital provides a dynamic environment for high-quality care, teaching, and cutting edge research.
Associate Director, Clinical Operations Harmony Biosciences Holdings IncAssociate Director, Clinical OperationsPlymouth Meeting, PAPrepares and/or reviews study-related and essential clinical study start-up documents (e.g., Clinical protocols, Informed consent forms, Investigator Brochures, Pharmacy Manual, Monitoring Plan, Laboratory Manual, Patient Diary, Clinical Site Procedures Manual, Pharmacy Manual, Case Report Form (CRFs), CRF Completion Guidelines and other relevant study plans and charters). Responsibilities include but are not limited to: Responsible for the oversight of trial-level operations for existing and/or future clinical studies, including but not limited to protocol concept design, CRO and vendor selection, CRO oversight, investigator meetings, etc.
NewClinical Outsourcing Lead Integrated Resources, IncClinical Outsourcing LeadCollegeville, PennsylvaniaFull timeJob DescriptionTechnical Skill RequirementsFinance / clinical budgetingDemonstrates clear understanding of activity based costs along study path; additionally, Director Level (P05) demonstrates expertise in strategic cost relationships and links (program, asset, portfolio, etc.) for planning and forecasting, negotiation, and higher level presentationUnderstands components of clinical & per subject costing & use of industry benchmarkingOperational expertise in study scheduling and placementKnowledge of clinical study outsourcing; Director Level (P05) requires expert knowledge in clinical trial development outsourcingUnderstanding of operational impact to timelines, budget, and quality desired, and required for Director Level (P05)Negotiating and contracting skillsKnowledge and experience of contracting with external service providersApplication of contracting strategies at enterprise levelsInternal and external influencing abilities for expectation and timeline management; for Director Level (P05), proven experience requiredIdentifies and leads efforts to examine multiple solutions or innovative options in solving highly complex problems directly impacting a Global Business Unit/Global Operating Unit or Sub Business Unit/Sub Operating UnitQualificationsQualificationsBA or BS degree and/or recognized amount of work experience (preferably in a related discipline).An advanced degree (MBA, JD, etc.), prior management responsibilities, and/or substantial work experience is preferential for the Director Level (P05).Clinical trials Sponsor experience, CRO operational and/or BD experience, or other trial related experience, including significant experience negotiating and drafting clinical trial-related agreements is required. Excellent oral/written communication skills and proficiency with MS Office applications (Word/PPT/Excel) required: experience with ACW, ClearTrial, Grants Manager and / or other industry cost and planning tools preferred.
NewClinical Dictionary Analyst Integrated Resources, IncClinical Dictionary AnalystMalvern, PennsylvaniaFull timeUndertake coding and review of verbatim terms when necessary to successfully meet project timelinesEnsure coders adhere to establish processes/proceduresCommunicate progress and issues related to coding assignments to Head, Dictionary Group and DML/CDM (as appropriate)Assist in identifying and implementing new dictionaries and software improvements (ds Navigator, eDM, etc.)Assist in development and maintenance of Dictionary SOPs and Working InstructionsAssist Coders in writing and resolving dictionary queriesUndertake sample based Q.C. of synonym additions. Clinical Dictionary Analyst - The Global Dictionary Analyst is responsible for facilitating Dictionary management processes, including maintaining and supporting the development of clinical dictionaries used in clinical data analysis.
Clinical Veterinarian (Sr. or Associate) Temple UniversityClinical Veterinarian (Sr. or Associate)Philadelphia, PAThe Clinical Veterinarian includes the provision of hands-on clinical care for all animals under the care of ULAR, i.e. mice, rats, dogs, cats, sheep, pigs, aquatics, reptiles, etc. and participates as needed with research procedural support to include research related surgical procedures. Experience with rodent surgical models, rodent technical procedures, USDA species technical procedures, and models, i.e. sheep, pig, dog, cat, rodent breeding colonies, genetically altered animals, aquatics procedures, and rodent medicine experience is preferred.
Research Postdoctoral Fellow - DeRaedt Lab Children's Hospital of PhiladelphiaResearch Postdoctoral Fellow - DeRaedt LabPhiladelphia, PAMHCII antigen presentation/myeloid mimicry: Elucidate the role MHCII expression in NF1 HGG tumor cells (see poster ISPNO, Molecular Cancer Therapeutics) Advanced preclinical modeling: Optimizing tumoroid/organoid cultures for NF1 associated high- and low-grade glioma (see poster ISPNO). If you are applying for a Research Post-Doctoral Fellow role, please refer to this link for salary guidelines (copy & paste into your browser): https://www.research.chop.edu/services/hiring-a-postdoctoral-fellow#collapse-accordion-3523-3 .
Research Postdoctoral Fellow - Magnetic Resonance Spectroscopy Children's Hospital of PhiladelphiaResearch Postdoctoral Fellow - Magnetic Resonance SpectroscopyPhiladelphia, PAIf you are applying for a Research Post-Doctoral Fellow role, please refer to this link for salary guidelines (copy & paste into your browser): https://www.research.chop.edu/services/hiring-a-postdoctoral-fellow#collapse-accordion-3523-3 . As a Program in Advanced Imaging Research (PAIR) member at CHOP, the individual can participate in outreach events and attend lectures and seminars on various diseases and development research, allowing exposure to scientific and clinical leaders in the field.
Research Project Interviewer - On Site - Philadelphia SAGOResearch Project Interviewer - On Site - PhiladelphiaPhiladelphia, PAThe Research Project Interviewer (RPI) plays a critical role in the successful execution of research studies by supporting subject recruitment, informed consent, study visits, investigational product handling, and study documentation. Collaborate effectively with monitors, the Clinical Project Management team, and site staff to support overall study success.
Senior Clinical Research Associate - Psychiatry - East Coast (Remote) Worldwide Clinical Trials Holdings IncSenior Clinical Research Associate - Psychiatry - East Coast (Remote)PARemote$97,000–$193,000 / yearTypically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-related events, managing the site's activities during study maintenance, and closing down research activities at the sites once the study has concluded. As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases.
Appeals and Grievances Clinical Specialist HealthfirstAppeals and Grievances Clinical SpecialistPA$83,100–$120,360 / yearPosition Summary: The Appeals & Grievances (A&G) unit manages Healthfirst member complaints, grievances and appeals that are presented by the member or provider pertaining to the authorization of or delivery of clinical and non-clinical services. Prepare cases 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.
Clinical Research Nurse Tower HealthClinical Research NursePhoenixville, PennsylvaniaFull timeAdditionally, the system provides a wide range of healthcare services, such as Reading Hospital Rehabilitation at Wyomissing, home healthcare via Tower Health at Home, TowerDirect ambulance and emergency response, Tower Health Medical Group, Tower Health Providers (a clinically integrated network), and Tower Health Urgent Care facilities across its service area. Committed to academic medicine and training, Tower Health offers various programs, including residency and fellowship programs, the Drexel University College of Medicine at Tower Health, and the Reading Hospital School of Health Sciences.
Clinical Research Regulatory Coordinator CNI Cooper University Health CareClinical Research Regulatory Coordinator CNICamden, NJThis role supports study startup, maintenance, and closeout by managing submissions to regulatory agencies, maintaining Investigator and staff documentation, and facilitating communication among Investigators, sponsors, and institutional offices. The Clinical Research Regulatory Coordinator ensures regulatory compliance and accurate documentation for all clinical research studies conducted at Cooper University Health Care.
Clinical Research Nurse I Cooper University Health CareClinical Research Nurse ICamden, NJOur extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. Responsible for completing and maintaining all study documents, in compliance with IRB, Cooper Health System, sponsor and FDA requirements.
Clinical Research Nurse I CNI Cooper University Health CareClinical Research Nurse I CNICamden, NJOur extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. Responsible for completing and maintaining all study documents, in compliance with IRB, Cooper Health System, sponsor and FDA requirements.
Clinical Research Coordinator II Cooper University Health CareClinical Research Coordinator IICamden, NJOur extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, and development of study budget.
Oncology Research Pre Post Award Associate Cooper University Health CareOncology Research Pre Post Award AssociateCamden, NJThe role of the Oncology Research Pre-Post Award Associate is to develop the clinical trial agreements, budgets and coverage analyses for industry sponsored clinical trials to bring new clinical trials to our patients and complete research billing review in Epic and facilitate research invoicing for industry sponsored and federally-funded clinical trials and work with the Clinical Research Coordinators and grants management colleagues to support accurate billing and invoicing. Invoice clinical trial sponsors for services provided to patients on clinical trial Maintains clinical billing procedures for research and identifies process improvement initiatives Structure, negotiate, draft, and review Clinical Trial Agreements for MD Anderson Cancer Center at Cooper with industry sponsors for research studiesUtilizes clinical expertise to interpret clinical treatment plans and medical documentation to determine appropriate billing of clinical research charges.
Research Associate RD PartnersResearch AssociatePhiladelphia, Pennsylvania£60,752–£75,957Perform release, characterization and stability testing of lentiviral products to support the analytical requirements of the process development and discovery teams, including but not limited to Western Blot, ELISA/Alphalisa, PCR-based methods, flow cytometry, particle analysis, and cell-based viral titration. · Demonstrated competency and experience with characterization of viral vectors using cell-based, molecular (qPCR/ddPCR) and/or traditional biochemical methods.
Associate Research Scientist RD PartnersAssociate Research ScientistLawrenceville, New Jersey£65,977–£82,472Experimental techniques could include, but are not limited to, the following: Processing human tissue and blood, Cell-based assays, Flow cytometry, ELISAs/MSD assays, RNA extraction and cDNA synthesis, Gene expression array cards. The qualified candidate will process human samples, maintain the laboratory's biobank (including sample storage and retrieval), and perform a range of experimental procedures under the guidance of senior scientists.
Oncology Research Coord I Cooper University Health CareOncology Research Coord ICamden, NJ1.7 Develop, schedule, and oversee subject visits and any necessary testing and appointment coverage according to protocol and in accordance with Good Clinical Practice ("GCP") (e.g., scheduling subject visits within the appropriate window, ensuring all tests and assessments at each visit are performed, reporting adverse events and ensuring review and appropriate follow-up by investigator, documenting in EPIC any patient-reported symptoms and forwarding to the appropriate clinical team, monitoring patient care and treatment side effects in concert with investigators, detailed documentation of study activities). 1.5 Active in planning and implementation of patient recruitment into studies; reviewing medical records of upcoming new and return patient clinic visits and discussing with investigators, reaching out to potential referring physicians, approaching potential subjects in the office or speaking to them by phone, asking pre-screening eligibility questions, etc., and document in the electronic medical record system, EPIC.
Oncology Research Nurse Nav I PRN Cooper University Health CareOncology Research Nurse Nav I PRNCamden, NJ5.3 Provides education within the Cooper network and outside the institution as needed.5.4 Provides educational programs and lectures for oncology fellows, surgical residents, medical students, and nurses.5.5 Assists with onboarding and training of new research staff and other CCI faculty. Identifies areas in which the patient/family lack knowledge, then provides supportive information/teaching, incorporating the patient's cultural/spiritual beliefs.2.5 Facilitates patient participation and control in clinical decision-making while providing emotional and informational support to the patient and family.
Associate Director, Clinical R&D QA US Incyte CorpAssociate Director, Clinical R&D QA USWilmington, DEAssist with the maintenance of the clinical Quality Management System including QA support for change control deviations reviewrevision of SOPs with ensuring continuous process improvement Stay abreast of clinical trial requirements ICH GCP and guidelines from other regulatory agencies for the management of clinical trials as appropriate. Be thoroughly familiar with assigned Incyte Compounds and protocol REQUIREMENTS Bachelors degree in a science or healthcare related discipline or similarly conferred degree from a university 5 to 7 years experience in a pharmaceutical or bio-pharmaceutical company in a GCP QA role or Clinical compliance role.
Associate Clinical Consultant (Salt Lake City, UT) - Johnson & Johnson MedTech – Heart Recovery 6942-ABIOMED Legal EntityAssociate Clinical Consultant (Salt Lake City, UT) - Johnson & Johnson MedTech – Heart RecoveryCherry Hill, New JerseyBusiness Behavior, Customer Centricity, Customer Effort Score, Execution Focus, Goal Attainment, Innovation, Market Expansion, Market Research, Medicines and Device Development and Regulation, Product Knowledge, Sales Engineering, Solutions Selling, Sustainable Procurement, Vendor Selection Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Business Development Manager, ADME, DMPK, Toxicology Preclinical Research Services (Copy) RPM ReSearchBusiness Development Manager, ADME, DMPK, Toxicology Preclinical Research Services (Copy)Philadelphia, PennsylvaniaResponsibilities: • Identify opportunities to coordinate client contact with Government agencies, biotech/pharmaceutical companies (both prospective and current clients of Company), to market and ensure customer satisfaction with Company services. Overview: Rapidly Growing mid-size Preclinical Contract Research Organization (CRO) is expanding its West Coast Territory with another Director of BD to support continued growth.
Research Assistant Part Time Cooper University Health CareResearch Assistant Part TimeCamden, NJWorking knowledge of general principles in genetics and molecular biology, as well as accurate and timely record keeping, careful organization, and demonstrated interest in working in a laboratory setting is needed to excel in this role• Have prior experience in a biological research laboratory and experience working with rodents in a wet lab setting • Ability to analyze research results using statistical software• Demonstrated computer skills and proficiency with MS Office suite or similar spreadsheet, database, word processing and presentation software• Ability to work in a collaborative, team-oriented environment, and strong communication skills are required• Ability to work early mornings, evenings, and weekends to administer study protocols, as necessary. Assists the Principal Investigator and other members of the research team with preparation of IRB protocols, consent forms, continuing reviews, amendments, and maintenance of study budget.
Associate Clinical Director K3 Neuro ICU Cooper University Health CareAssociate Clinical Director K3 Neuro ICUCamden, NJActing as a liaison between nursing and medical staff, serving as a problem-solver and mediator for positive change; develops and maintains effective intra and interdepartmental relationships. Our nurses provide expert neurological care in both settings to ensure seamless continuity of care for our patients across a wide range of neurological diagnoses.
Associate Clinical Consultant (Albuquerque, NM) - Johnson & Johnson MedTech – Heart Recovery 6942-ABIOMED Legal EntityAssociate Clinical Consultant (Albuquerque, NM) - Johnson & Johnson MedTech – Heart RecoveryCherry Hill, New JerseyBusiness Behavior, Customer Centricity, Customer Effort Score, Goal Attainment, Innovation, Market Expansion, Market Research, Medicines and Device Development and Regulation, Problem Solving, Product Knowledge, Sales Engineering, Solutions Selling, Sustainable Procurement, Vendor Selection Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity.
Clinical Documentation Educator, Remote CPC and/or CCS P Required Cooper University Health CareClinical Documentation Educator, Remote CPC and/or CCS P RequiredCamden, NJRemoteReporting to the Manager of the Clinical Documentation Team the Clinical Documentation Educator, through diverse assignments, supports and participates in educational activities to improve of the quality, completeness and accuracy of clinical documentation for Cooper University Physicians (CUP.). Well-versed in using, referring to and researching CMS and other federal and local clinical documentation and compliance guidelines, CPT, ICD-9-CM and HCPCS codes, Evaluation and Management Documentation Guidelines and PATH guidelines.
Associate Director/Director, Clinical Supply Savara IncAssociate Director/Director, Clinical SupplyPennsylvania, PARemote$140,000–$200,000 / yearReporting to the Executive Director, Logistics & Supply Chain, the Associate Director/Director, Clinical Supply will be instrumental in ensuring the availability of supply to patients currently receiving Molgramostim treatment in our clinical trial and expanded access programs. With guidance from the Executive Director, Logistics & Supply Chain, maintains the overall labeling, packaging, and distribution strategy for all investigational programs.
Clinical Coord Program LPN PRN Cooper University Health CareClinical Coord Program LPN PRNCamden, NJCommunicates with providers, inpatient clinical directors, and other multidisciplinary team members status updates on RPM program enrollment as needed 4. Reviews patient agreement with patient and ensures signed, and scanned into patient EPIC electronic health record5. Roles and responsibilities could include digital platform enrollment and alert monitoring, telephonic patient outreach and education, coordination and escalation of care, and communication and collaboration with the providers and multidisciplinary team.
Scientific Writer and Research Analyst (Posting Title) American Association for Cancer ResearchScientific Writer and Research Analyst (Posting Title)Philadelphia, PennsylvaniaFull timeIn this role, the candidate will contribute to the preparation of high-impact scientific documents—such as cancer progress reports, white papers, and scholarly articles—that highlight advances in blood cancer and communicate their significance to diverse audiences, including basic and clinical scientists, clinicians, policymakers, patient advocates, and the public. Overview: We are seeking a highly skilled and motivated Scientific Research Analyst with deep expertise in one or more major subtypes of blood cancer and other related syndromes (leukemia, lymphoma, multiple myeloma, MDS, CHIP).
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.
Director, Clinical Quality Assurance Braeburn IncDirector, Clinical Quality AssurancePlymouth Meeting, PARemoteSkills: • Established GCP QA professional • Robust understanding of quality management systems and GxP to ensure compliance with regulatory requirements • Excellent critical data analysis, written, and oral communication skills • Strong experience in QA Audits of Clinical sites and Third-party organizations • Demonstrated ability to successfully interact with regulatory health authorities at inspections as well as lead all preparation, hosting, and follow-up activities • Ability to lead and influence cross functional employees to ensure compliance, and able to enhance team performance through strong collaboration skills • Robust knowledge of successful delivery of a clinical study, e.g., ICH-GCP, study management, site management, monitoring, SOPs, training, etc. Education/Experience: • BA/BS in related field with at least 10 years of Quality Assurance experience in pharmaceutical GCP operations or related quality technical role in the medical space • Deep knowledge of international guidelines ICH-GCP as well as relevant local regulations • Significant experience with QA review of Clinical Protocols, CAPA reports, SOPs, change control processes, deviation/investigation reports, computer systems validation, QA agreements, audit reports • Experience utilizing QMS metrics, KPIs, and QTLs to assess risks to clinical research and drug development processes • Demonstrated expertise in leading organizational and planning activities.
Medical Director, Rheumatology - Clinical Development KaztronixMedical Director, Rheumatology - Clinical DevelopmentChesterbrook, PAThis physician leader will play a critical role in advancing therapeutic programs from early development through late-stage clinical studies by providing strategic medical leadership, scientific expertise, and cross-functional collaboration. The position requires deep knowledge of rheumatologic and autoimmune diseases, strong clinical judgment, and experience contributing to drug development programs in biotechnology or pharmaceutical settings.
Executive Director, Clinical Scientist Madrigal Pharmaceuticals IncExecutive Director, Clinical ScientistConshohocken, PA$288,000–$352,000 / yearProviding strategic and scientific leadership across clinical programs, driving study design, execution, and cross-functional alignment to advance assets through development and toward regulatory milestone, the Executive Director, Clinical Scientist will: Contribute to the design and development of clinical trial protocols, including scientific rationale, study objectives, endpoints, and eligibility criteria. Please 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.
NewClinical Operations Administrative Support PSI CRO AGClinical Operations Administrative SupportKing of Prussia, PAAs a Clinical Operations Administrative Support (COAS) you will provide administrative and operational support to clinical trial project teams, helping ensure studies are conducted efficiently, documentation is maintained accurately, and clinical sites receive the support they need throughout the trial lifecycle. College or university science degree or an equivalent combination of education, training and experience that presents the required knowledge, skills and abilities is considered sufficient.
Clinical Advisor - Oncology & Rare Disease Products (BCOP) CVS Health CorpClinical Advisor - Oncology & Rare Disease Products (BCOP)PARemote$135,575–$228,800 / yearDevelop cost management and population health programs such as formulary and coverage strategies, prior authorization programs, care management programs, patient and provider engagement programs, value-based arrangements, and more to promote the delivery of high-quality, safe, and effective programs which optimize health outcomes, improves the provider and member experience, and reduces costs for clients and members. This position will be responsible for driving growth in Specialty by 1) building innovative products that secure our position as the market leader in payor focused Specialty solutions and 2) creating disruptive and holistic solutions to address oncology, rare disease, and other high-cost therapies to ensure best in class management of cost and quality of care.
NewClinical Dictionary Analystma Integrated Resources, IncClinical Dictionary AnalystmaMalvern, PennsylvaniaContractorUndertake coding and review of verbatim terms when necessary to successfully meet project timelinesEnsure coders adhere to establish processes/proceduresCommunicate progress and issues related to coding assignments to Head, Dictionary Group and DML/CDM (as appropriate)Assist in identifying and implementing new dictionaries and software improvements (ds Navigator, eDM, etc.)Assist in development and maintenance of Dictionary SOPs and Working InstructionsAssist Coders in writing and resolving dictionary queriesUndertake sample based Q.C. of synonym additions. Job DescriptionClinical Dictionary Analyst - The Global Dictionary Analyst is responsible for facilitating Dictionary management processes, including maintaining and supporting the development of clinical dictionaries used in clinical data analysis.
Director, Clinical Scientist Madrigal Pharmaceuticals IncDirector, Clinical ScientistConshohocken, PA$215,000–$264,000 / yearProviding strategic and scientific leadership across clinical programs, driving study design, execution, and cross-functional alignment to advance assets through development and toward regulatory milestone, the Director, Clinical Scientist will: Contribute to the design and development of clinical trial protocols, including scientific rationale, study objectives, endpoints, and eligibility criteria. Please 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.
Clinical Practice Specialist MA Float Pool Cooper University Health CareClinical Practice Specialist MA Float PoolCamden, NJMay be involved in both the clinical and administrative areas including assisting providers with patient care, and handling clerical, environmental, and organizational tasks. Our extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols.
NewClinical Care Reviewer Integrated Resources, IncClinical Care ReviewerPhiladelphia, PennsylvaniaFull timeUsing clinical knowledge and nursing experience, the nurse reviews provider requests for inpatient and outpatient services, working closely with members and providers to collect all information necessary to perform a thorough medical necessity review. The nurse will use his/her professional judgment to evaluate the request to ensure that appropriate services are approved and recognize care coordination opportunities and refer those cases as needed.
Research Technician III Children's Hospital of PhiladelphiaResearch Technician IIIPhiladelphia, PA$48,200–$60,200 / yearDr Tasian's translational laboratory in the Division of Oncology and Center for Childhood Cancer Research focuses upon the development of new treatments for high-risk childhood leukemias with an emphasis upon small molecule inhibitor therapies and cellular (CAR T cell) immunotherapies. Dr Tasian is seeking a motivated, dynamic, and hard-working Research Technician to join her laboratory to assist with preclinical animal model studies and with correlative biology studies for childhood leukemia clinical trials using primary patient samples.
Senior Director, Clinical Scientist Madrigal Pharmaceuticals IncSenior Director, Clinical ScientistConshohocken, PA$260,000–$318,000 / yearProviding strategic and scientific leadership across clinical programs, driving study design, execution, and cross-functional alignment to advance assets through development and toward regulatory milestone, the Senior Director, Clinical Scientist will: Contribute to the design and development of clinical trial protocols, including scientific rationale, study objectives, endpoints, and eligibility criteria. Please 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.
Clinical Nurse Manager Kelemen 8 South Cooper University Health CareClinical Nurse Manager Kelemen 8 SouthCamden, NJShort Description The Clinical Nurse Manager will provide the knowledge, skill, and expertise necessary to successfully support the day to day operations of the clinical unit. Experience Required A minimum of 2 years of clinical nursing experience in an acute care setting, with 1 year of demonstrated leadership abilities.
NewClinical Scientist Integrated Resources, IncClinical ScientistCollegeville, PennsylvaniaContractorD. Degree in science or health-related field preferred, will consider highly motivated and experienced MA or MS• 10+ years of pharmaceutical/CRO experience preferredTECHNICAL SKILLS:• Has extensive knowledge of the clinical research process and Good Clinical Practices from previous employment experience in the clinical research field• Has demonstrated ability and level of experience with integrating and summarizing medical/scientific concepts in protocols and other clinical documents• Has independently authored clinical study documents• Has experience with participating in and informally leading an operational team• Applies knowledge of internal/external business challenges to facilitate process improvements• Has ability to proactively resolve issues and work independently with minimal supervision• Has working knowledge of statistics, data analysis, and data interpretation• Has exceptional written and oral communication and cross-functional collaborative skills• Is proficient in MS Word, Excel, and PowerPointJob LocationI'm interested Clinical ScientistA 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.
Research Study Assistant (Non-therapeutic trails) Temple HealthResearch Study Assistant (Non-therapeutic trails)Philadelphia, 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.