NewClinical Dietitian AramarkClinical DietitianPhiladelphia, PAAbout the Hospital: Temple Health - Chestnut Hill Hospital is a 148-bed community-based inpatient and outpatient facility offering diagnostic and treatment services, including emergency care, minimally invasive laparoscopic and robotic-assisted surgery, cardiology, gynecology, oncology, and orthopedics, and two Women's Centers. So, no matter what you're pursuing - a new challenge, a sense of belonging, or just a great place to work - our focus is helping you reach your full potential.
NewClinical Regional Manager Inizio EngageClinical Regional ManagerPhiladelphia, PA$109,000–$202,000 / yearOur passionate, global workforce augments local expertise and diverse mix of skills with data, science, and technology to deliver bespoke engagement solutions that help clients reimagine how they engage with their patients, payers, people, and providers to improve treatment outcomes. Must have at least five (5) years of recent oncology nursing experience and at least five (5) years of general nursing experience that includes, but is not limited to direct patient care, physical assessment, patient education, group in servicing, and proficiency in peripheral IV access.
Senior Clinical Trial Case Manager CSLSenior Clinical Trial Case ManagerKing of Prussia, PAManages case management activities for assigned clinical studies to ensure compliance with national and international regulations, such as GxP guidelines and/or other relevant international and national legislation, regulations, guidance, and company policies and procedures within the area of responsibility. Develops, implements, and oversees pharmacovigilance procedures and processes and ensures the uniform and timely processing and analysis of safety data to comply with regulatory requirements.
Associate Director, Clinical Trial Disclosure & Transparency CSLAssociate Director, Clinical Trial Disclosure & TransparencyKing of Prussia, PAThis role guides global strategy, drives process excellence, and oversees the delivery of clinical trial disclosure activities including registration, results disclosure and layperson summaries while providing support for transparency activities including anonymization and redaction of commercially confidential information (CCI) as required for business continuity and operational needs. The Associate Director Clinical Trial Disclosure and Transparency is a global subject matter expert responsible for ensuring timely, accurate, and compliant clinical trial disclosures across all regions and study types (interventional and observational).
Global Clinical Lead- Hematology CSLGlobal Clinical Lead- HematologyKing of Prussia, PAReporting to the Head, Global Clinical Development the Global Clinical Lead (GCL) will act in a key leadership role in the Clinical Development (CD) group; Providing strategic and tactical Medical & Scientific leadership and guidance for clinical development activities for 5-8 Global Clinical Program Leaders (GCPL). May act as any of the following roles in clinical development: GCPL, Early Clinical Development Lead, Business Development (BD) Contributor, Product Strategy Team (PST) Clinical Representative, Clinical Development Team (CDT) Lead, or a Clinical Study Lead as appropriate for projects as assigned per business need.
Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate) Medpace, Inc.Clinical Research Coordinator to Home-Based CRA (Clinical Research Associate)Philadelphia, PennsylvaniaRemoteOn-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
Clinical Research Coordinator to Home Based CRA (Clinical Research Associate) Medpace Holdings IncClinical Research Coordinator to Home Based CRA (Clinical Research Associate)Philadelphia, PARemoteOn-site and virtual/remote monitoring activities with a risk-based monitoring approach (including centralized data review) through our integrated Clinical Trial Management System to identify site deviations/deficiencies and corrective/preventive actions to bring a site back into compliance and mitigate risks moving forward. When you join Medpace, you become part of an innovative team that brings cutting-edge therapies to market while building a meaningful and rewarding career focused on scientific excellence and improving patient outcomes around the world through continuous learning and cross-functional collaboration.
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.
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.
Director Clinical Applications -Clinical Applications Team Thomas Jefferson UniversityDirector Clinical Applications -Clinical Applications TeamMontgomery County, PAJefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research. Thomas Jefferson University, home of Sidney Kimmel Medical College, Jefferson College of Nursing, and the Kanbar College of Design, Engineering and Commerce, dates back to 1824 and today comprises 10 colleges and three schools offering 200+ undergraduate and graduate programs to more than 8,300 students.
Clinical Trial Manager, Clinical Operations Madrigal Pharmaceuticals IncClinical Trial Manager, Clinical OperationsConshohocken, PA$143,007–$168,465 / yearThe Clinical Trial Manager partners closely with other members within Clinical Operations, cross-functional functional areas, CROs, vendors, and investigational sites to drive successful study execution across multiple phases of clinical development. The role serves as the primary operational lead for assigned studies, mentors Associate Clinical Trial Managers and Clinical Trial Specialists, and contributes to process improvements that enhance operational efficiency while ensuring compliance with ICH-GCP, applicable regulatory requirements, and company SOPs.
Clinical Research Project Manager B University of PennsylvaniaClinical Research Project Manager BPhiladelphia, PA$74,500–$95,000 / yearThe FTDC is seeking a Clinical Research Project Manager B (PM-B) who will be responsible for day-to-day management and oversight of the FTDC's federally funded observational research portfolio focused on young onset neurodegenerative diseases including frontotemporal degeneration (FTD), Alzheimer's disease and related dementias. 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.
Clinical Research Program Manager University of PennsylvaniaClinical Research Program ManagerPA$75,804–$81,441 / yearThe Program manager will work closely with major internal (PI, data coordinators, researcher, laboratory technician, students, Institutional Review Board (IRB), etc.) and external (pharmaceutical collaborators, non-profit partners, external collaborators, oversight boards, CROs, Subcontractors, etc.) stakeholders to ensure regulatory compliance, completion of project milestones, and completion of all reporting requirements, and correct allocation of resources. Strong organizational skills; experience conducting studies in one or more of the above content areas preferred; excellent verbal and written communication skills essential to enable working with multiple members of research team; must be highly skilled in MS Word and Excel applications, understand medical records/patient charts organization and terminology.
Pathology- Chief of Clinical Pathology & Medical Director of Clinical Laboratories Temple University, Office of Physician & Faculty RecruitmentPathology- Chief of Clinical Pathology & Medical Director of Clinical LaboratoriesPhiladelphia, PennsylvaniaSummary of Position: The Department of Pathology & Laboratory Medicine at the Lewis Katz School of Medicine at Temple University invites applications for an accomplished leader to serve as Chief of Clinical Pathology for Temple University Health System (TUHS) and Medical Director of Clinical Laboratories for Temple University Hospital – Health Sciences Campus and TUH – Jeanes Campus . Please address your application to: Yuri Persidsky, MD, PhD, Professor and Chairperson, Department of Pathology and Laboratory Medicine, C/O Bill Mawhinney, Senior Recruiter, Physician/Faculty Recruitment & Retention, Lewis Katz School of Medicine at Temple University, Email: William.
Clinical Research Project Manager A/B University of PennsylvaniaClinical Research Project Manager A/BPA$63,085–$89,789 / yearWith mentoring from the Principal Investigator and Associate Director, the Clinical Research Project Manager A/B will take a leadership role in developing study protocols, managing the detailed operations of projects, coordinating activities in single center and/or multi-center studies, assisting with quality control, and assisting with grant applications when applicable. 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.
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 Project Manager A University of PennsylvaniaClinical Research Project Manager APhiladelphia, PA$63,085–$75,000 / yearAs part of the Department of Medicine, the DOM Clinical Trials Unit supports a diverse group of investigators, involving work on a wide spectrum of clinical trials ranging from phase I to IV, investigator and industry initiated, different disease states and varying complexities. The person will work closely with the Director of Clinical Research Operations to support a diverse group of investigators and coordinators, involving work on a wide spectrum of clinical trials ranging from phase I-IV, investigator/industry-initiated, different disease states and varying complexities.
Clinical Research Project Manager B (Department of Obstetrics and Gynecology) University of PennsylvaniaClinical Research Project Manager B (Department of Obstetrics and Gynecology)Philadelphia, PA$75,804–$89,789 / yearThe Gynecologic Oncology research program has seen substantial growth in the volume and complexity of Phase 1-3 clinical trials, This role will provide essential high-level oversight and coordination of our expanding trial portfolio, including study activation, regulatory compliance, sponsor/CRO interactions, cross-functional team management, and process improvement initiatives. The PM will oversee patient education for complex trials assuring that study activities and procedures are explained to patients and family members in lay terms and utilizing teach back methods to confirm patients and families understand what is required to participate in the study.
Clinical Research Monitor II Temple University Health SystemClinical Research Monitor IIPhiladelphia, PA404810'',''true'',''404810'',''false'',''Submission for the position: Clinical Research Monitor II - (Job Number: 263138)'',''false'',''404810'',''false'',''true'',''Clinical Research Monitor II'',''263138'',''!*!The OCR Clinical Research Monitor II, completes, revises and reviews the requirements necessary to attaining and maintaining compliance with the FDA and other regulatory bodies for clinical trial research both from a documentation and process level. '',''Pennsylvania-Philadelphia'',''Pennsylvania-Philadelphia'',''Research & Science'',''Research & Science'',''Full-time'',''Full-time'',''Day Job'',''Day Job'',''Regular'',''Regular'',''false'',''404810'',''404810'',''true'',''404810'',''false'',''Submission for the position: Clinical Research Monitor II - (Job Number: 263138)'',''false'',''404810'',''false'',''true''.
Clinical Research Project Manager Thomas Jefferson UniversityClinical Research Project ManagerPhiladelphia, Pennsylvania5501 Old York Road, Philadelphia, Pennsylvania, United States of America Nationally ranked, Jefferson, which is principally located in the greater Philadelphia region, Lehigh Valley and Northeastern Pennsylvania and southern New Jersey, is reimagining health care and higher education to create unparalleled value. Jefferson is more than 65,000 people strong, dedicated to providing the highest-quality, compassionate clinical care for patients; making our communities healthier and stronger; preparing tomorrow's professional leaders for 21st-century careers; and creating new knowledge through basic/programmatic, clinical and applied research.