Clinical Trial Research Monitor II Temple University Health SystemClinical Trial Research Monitor IIPhiladelphia, PAThe 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. Other applicable certification, related training, or education programs may be considered in lieu of those listed below (i.e. Regulatory Affairs).
NewPsychiatrist - Principal Investigator, Clinical Research (1099/Part-Time) Hawthorne HealthPsychiatrist - Principal Investigator, Clinical Research (1099/Part-Time)Lindenwold, New JerseyAbout Us Hawthorne Health is a leading community site network and home research visit solution provider, with 20+ sites and more than 2,000 research experienced healthcare professionals across the U.S. Hawthorne leverages convenient, trusted, healthcare locations, identified patient data, and intelligent technology to accelerate patient access, improve retention, and reduce study costs. The Principal Investigator will lead sponsor-initiated psychiatric clinical trials, including studies focused on conditions such as anxiety and depression , while working alongside an experienced team of Sub-Investigators, Clinical Research Coordinators, and centralized clinical operations professionals.
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.
Clinical Pharmacist – Emergency Department - Per Diem Capital HealthClinical Pharmacist – Emergency Department - Per DiemPennington, New JerseyOccasional physical demands include: Climbing (e.g., stairs or ladders), Carry objects, Push/Pull, Twisting, Bending, Reaching forward, Reaching overhead, Squat/kneel/crawl, Wrist position deviation, Pinching/fine motor activities, Talk or Hear. Demonstrates teamwork within Pharmacy Department and participate in group approach to patient care by providing support to peers and other practice areas as needed in addition to daily assignments.
Clinical Pharmacist - Emergency Department - Per Diem Capital HealthClinical Pharmacist - Emergency Department - Per DiemPennington, NJOccasional physical demands include: Climbing (e.g., stairs or ladders), Carry objects, Push/Pull, Twisting, Bending, Reaching forward, Reaching overhead, Squat/kneel/crawl, Wrist position deviation, Pinching/fine motor activities, Talk or Hear. Demonstrates teamwork within Pharmacy Department and participate in group approach to patient care by providing support to peers and other practice areas as needed in addition to daily assignments.
Clinical Research Coordinator - Autism Research The Children's Hospital of PhiladelphiaClinical Research Coordinator - Autism ResearchPhiladelphia, PennsylvaniaAs part of the hospital’s Omics and Big Data efforts and the Lurie Autism Center, the Children’s Hospital of Philadelphia is hiring a research team member to support activities of the institutional-wide biobank in the Lurie Autism Center. Under moderate supervision from study PI or other research study management staff, coordinates all clinical research activities within the scope of clinical research protocols.
Clinical Research Coordinator A/B University of PennsylvaniaClinical Research Coordinator A/BPhiladelphia, PA$46,500–$56,274.86 / yearCoordinate the administration of the investigational product and study related medications including obtaining orders, scheduling administration dates, administration of investigational and study related medications (as applicable), monitoring subjects for post-administration adverse events or reactions. 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 Manager, Clinical Scientist Gan & Lee PharmaceuticalsSenior Manager, Clinical ScientistNJFull timeExperiences in metabolic diseases (Diabetes, Obesity, NASH, NAFLD, etc.), Endocrinology (CKD, CRF, etc.), and Nutrition and Weight Management related drug development are a plus. The position will work with Gan & Lee clinical program lead(s) to provide the scientific and clinical leadership and inputs in meeting the development objectives for the program.
Clinical Research Associate II/III - US Optimapharm ddClinical Research Associate II/III - USPhiladelphia, PARemoteWith operations in 40+ countries and 2x the patient reach of the average mid-sized CRO, we enable accelerated regulatory pathways, faster study start-up, and access to diverse patient populations worldwide. As we expand our US Clinical Operations team, we're searching for a CRA II/III who is motivated by quality, driven by purpose, and eager to contribute to innovative clinical research that changes lives.
Senior Clinical Data Manager (Remote - US) MMSSenior Clinical Data Manager (Remote - US)Philadelphia, PARemoteProvides oversight and resolves all issues in data management study processing activities including CRF tracking and data entry, integration of external electronic data (e.g., lab data) with clinical database, data validation and review, query processing and resolution, adverse event and medication coding, SAE reconciliation, database lock and database QC audits. Oversees and develops data management study documentation including Case Report Forms, CRF Completion Guidelines, Database Design via annotated CRFs, Validation specifications (edit checks), and Data Management Plan.
Clinical Data Manager ZSClinical Data ManagerPhiladelphia, PennsylvaniaAs a management consulting and technology firm focused on improving life and how we live it, we transform ideas into impact by bringing together data, science, technology and human ingenuity to deliver better outcomes for all. Proven Delivery Leadership: 10+ years of experience leading technology programs in a consulting environment, including direct ownership of scope, staffing, timelines, and delivery outcomes.
Clinical Nutrition Manager II - Healthcare Sodexo SAClinical Nutrition Manager II - HealthcareRED BANK, NJ$89,250–$115,500 / yearSodexo is seeking a Registered Dietitian for a Clinical Nutrition Manager position at Riverview Medical Center, a 475-bed acute care community hospital in Red Bank, NJ. Lead daily clinical nutrition operations for a large account, system, or multiple contracts, overseeing both non-exempt and entry-level professional staff.
NewClinical Trial Manager/Local Delivery Lead GSK plcClinical Trial Manager/Local Delivery LeadPhiladelphia, PA$115,500–$192,500 / yearAgile Thinking, Business Acumen, Clinical Development, Clinical Research, Clinical Research Trials, Clinical Sciences, Clinical Trial Designs, Clinical Trial Development, Clinical Trial Management, Clinical Trial Management Systems (CTMS), Clinical Trial Planning, Clinical Trial Protocols, Clinical Trials, Clinical Trials Operations, Communication, Creativity, Decision Making, Fostering Collaboration, Good Clinical Practice (GCP), Influencing Without Authority, Pharmaceutical Industry, Project Management, Time Management. Leads the local study team consisting of US clinical operations team members, cross functional experts (medical, regulatory, supply logistics, finance, legal, etc.), vendor staff and external clinical site staff involved in study preparation and delivery, providing both matrix leadership and project management of study activities within the United States.
Clinical Research Nurse SkyeliaClinical Research NurseNew JerseyScreen potential study participants and obtain informed consent prior to enrollment in research studies Administer study treatments, collect biological samples, and monitor participants throughout the study. Coordinate and manage patient care in line with protocol requirements, working closely with Principal Investigators and other healthcare professionals.
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.
Clinical Research Coordinator Flourish ResearchClinical Research CoordinatorPhiladelphia, PA$31–$36 / hourFlourish Research is one of the industry’s most progressive and diversified clinical trial organizations, with strong capabilities across cardiology, metabolic disorders, renal, oncology, CNS, pulmonology, and vaccine research. Excellent communication and interpersonal skills to effectively interact with the Principal Investigator, research team, Study Sponsor/CROs, potential subjects, and referral sources.
Senior Manager, Clinical Programming Genmab ASSenior Manager, Clinical ProgrammingPrinceton, 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. Please note that if you are applying for a position in the Netherlands, Genmab's policy for all permanently budgeted hires in NL is initially to offer a fixed-term employment contract for a year, if the employee performs well and if the business conditions do not change, renewal for an indefinite term may be considered after the fixed-term employment contract.
Lead Clinical Data Manager (Remote) IQVIA Holdings IncLead Clinical Data Manager (Remote)Philadelphia, PARemote$86,800–$217,100 / yearYour previous roles/job titles may include Clinical Data Manager, Senior Clinical Data Manager, Lead Data Manager, Principal Data Manager, and/or Data Management Project Manager. IQVIA is seeking experienced Senior Data Team Leads to oversee end-to-end data management delivery for global clinical trials.
Travel Clinical Research Coordinator Care Access Research LLCTravel Clinical Research CoordinatorPhiladelphia, PA$70,000–$100,000 / yearDue to enhanced experience in Care Access' decentralized clinical research process, the Travel Clinical Coordinator will be able to assume a greater study workload, overall study responsibility, and more detailed, Site, Sponsor and CRO interactions, while conveying a positive image of Care Access to the community, Sponsors, CROs, and study participants and their family members. With programs like Future of Medicine, which makes advanced health screenings and research opportunities accessible to communities worldwide, and Difference Makers, which supports local leaders to expand their community health and wellbeing efforts, we put people at the heart of medical progress.
Clinical Research Associate, Sponsor Dedicated IQVIA Holdings IncClinical Research Associate, Sponsor DedicatedCamden, NJ$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.