Senior Manager, Clinical Scientist, Hematology Regeneron Pharmaceuticals IncSenior Manager, Clinical Scientist, HematologyWarren, NJ$150,500–$245,500 / yearIn this role, you will lead the design, execution, and interpretation of clinical studies within a cross-functional matrix environment while collaborating closely with Medical Directors, Clinical Study Teams, and Global Clinical SubTeams to advance early- and late-stage development programs. We are seeking a Senior Manager, Clinical Scientist to join our Clinical Sciences team, supporting rare hematologic conditions and/or immunologic diseases.
Senior Clinical Trial Manager ICON PlcSenior Clinical Trial ManagerBlue Bell, PAClose collaboration with the assigned Local Trial Manager(s) (LTMs), Lead Site Manager (LSM), Site Managers (SMs), Clinical Trial Associates (CTAs), and Site Contract Managers (SCMs) to outline accountabilities/responsibilities and provide support and training, where necessary. The Sr LTM will manage and oversee the following throughout the study: Central IRB and other local vendors (Greenphire, Drug Destruction services, etc.…) including set up of vendor purchase orders, invoice review and approval, and change-orders, as applicable.
2027 Future Talent Program - Diversity and Inclusion in Clinical Trials (DICT) - Intern Merck & Co Inc2027 Future Talent Program - Diversity and Inclusion in Clinical Trials (DICT) - InternNorth Wales, PA$39,908–$111,111 / yearThis internship provides a unique opportunity to contribute to initiatives that help ensure clinical trials reflect the diverse populations impacted by disease and treatment outcomes. During the 12-week internship program, the intern will support one or more high-impact projects focused on identifying and addressing barriers to clinical trial participation among underrepresented populations.
Clinical Trial Supply (CTS) Study Manager CSL Behring LLCClinical Trial Supply (CTS) Study ManagerKing of Prussia, PAWe 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.
Travel Clinical Research Coordinator Care AccessTravel 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 Coordinator C (OBGYN - Pregnancy and Perinatal Research Center) University of PennsylvaniaClinical Research Coordinator C (OBGYN - Pregnancy and Perinatal Research Center)Philadelphia, PA$63,085–$67,046 / yearThe essential functions of the position include, but are not limited to: Serve as a senior clinical research coordinator for the NIH Environmental influences on Child Health Outcomes (ECHO) Program, independently managing complex protocol activities and participant follow-up with minimal supervision. 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 Data Manager SystimmuneClinical Data ManagerPrinceton, NJ$100,000–$170,000 / yearIndependently develop DM documents including but not limited to Data Management Plans (DMP), Case Report Forms (CRFs), CRF Completion Guidelines, Edit Checks, UAT specifications, centralized monitoring plans, data flow and integrity plans, blinding plans, and data review plans. The Clinical Data Manager (CDM) plays a broad role in interfacing with clinical study teams, external partners, and vendors to design, configure, and test clinical database systems, conduct data review, and support company deliverables.
Global Director, Clinical Project Management International Recruiting LLCGlobal Director, Clinical Project ManagementPrinceton, New JerseyIt specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). The company has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development.
Research Clinical Nurse Specialist DrexelResearch Clinical Nurse SpecialistPhiladelphia, PennsylvaniaConducts full CNS and research duties for assigned trials including Regulatory, IRB, and Study Start up and close out activities, staff training, recruitment, and retention of study subjects as noted below: Promptly documents and reports any observed protocol/trial issues to the IRB, Research Administrator and PI. Prepares and submits IRB documents under the direction of the Principal Investigator (PI), Research Administrator and prepares study related regulatory documents; Assists in development of contracts and budgets under direction of PI and Research Administrator.
Clinical Research Coordinator Actalent IncClinical Research CoordinatorPhiladelphia, PA$25–$31.25 / hourWe are seeking a dedicated Clinical Research Coordinator who will play a crucial role in supporting clinical trials by recruiting, screening, and enrolling subjects. We are proud to be an Engineering News-Record (ENR) Top 500 Design Firm for our engineering design services and a ClearlyRated Best of Staffing winner for both client and talent service.
Director, Clinical Data Management, Digital Health Technologies, Hybrid Merck & Co IncDirector, Clinical Data Management, Digital Health Technologies, HybridNorth Wales, PA$173,200–$272,600 / yearRequired Skills: Clinical Data Management, Data Validation, Decision Making, Digital Technology, Good Clinical Data Management Practice (GCDMP), Good Clinical Practice (GCP), People Leadership, Results-Oriented, Strategic Thinking, Support Management, System Improvements, Vendor Management. Experience working with internal (Clinical Sciences, BARDS, Global Clinical Trial Operations (GCTO), our Research & Development Division IT) and external (functional service providers, labs, investigator sites, etc.) stakeholders to deliver products and services supporting a portfolio of clinical trials/programs across multiple therapeutic areas.
Clinical Research Coordinator III Cooper University Health CareClinical Research Coordinator IIICAMDEN, NJOur extraordinary professionals are continuously discovering clinical innovations and enhanced access to the most up-to-date facilities, equipment, technologies and research protocols. In lieu of a nursing degree/License the following will be acceptable: 5 yrs of clinical research experience and up-to-date Clinical Research Certification.
Senior Principal Scientist, Clinical Research, Thoracic Malignancies Merck & Co IncSenior Principal Scientist, Clinical Research, Thoracic MalignanciesNorth Wales, PA$282,200–$444,200 / yearMonitoring and managing the conduct of ongoing or new clinical trials for investigational or marketed Oncology drugs; Analyzing and summarizing the clinical findings from studies to support decisions regarding safety and efficacy as well as new drug applications, clinical study reports, or publication; and. Assist the Senior/Executive Director in ensuring that appropriate corporate personnel are informed of the progress of studies of our Company's and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility.
Clinical Research Coordinator I - Rheumatology Children's Hospital of PhiladelphiaClinical Research Coordinator I - RheumatologyPhiladelphia, PA$53,000–$66,300 / yearThe clinical research coordinator will provide regulatory support for divisional Investigational Drug Application (IND) and Investigational Device Exemption (IDE) studies, day-to-day study management and facilitation of clinical trials, recruitment of patients into clinical research studies, and on-boarding support for team members. Ledby Clinical Research Director, Pamela Weiss, MD, MSCE, the Rheumatology Research Core is seeking an experienced Clinical Research Coordinator to work alongside a team of research support staff.
Clinical Research Coordinator II - Neuro-Oncology and Neurofibromatosis Children's Hospital of PhiladelphiaClinical Research Coordinator II - Neuro-Oncology and NeurofibromatosisPhiladelphia, PA$58,300–$72,900 / yearOur group aims to grow novel clinical trials within the Children's Hospital of Philadelphia, but we are also active members of neuro-oncology clinical research consortia, such as NFCTC and PNOC, and collaborate broadly with institutions through the US and internationally. Dr. Cassie Kline is the Director of Clinical Research for Neuro-Oncology, and also serves as the Director of Data Quality and Integration of the Pediatric Neuro-Oncology Consortium (PNOC).
Clinical Research Coordinator II - Pulmonary and Sleep medicine Children's Hospital of PhiladelphiaClinical Research Coordinator II - Pulmonary and Sleep medicinePhiladelphia, PA$58,300–$72,900 / yearUnder minimal supervision, this role substantially coordinates all clinical research activities within the scope of clinical research protocols. Develop informed consent document and/or draft or edit IRB protocols or related documents such as study administration manuals.
Clinical Research Assistant I - The Center for Injury Research and Prevention (CIRP) Children's Hospital of PhiladelphiaClinical Research Assistant I - The Center for Injury Research and Prevention (CIRP)Philadelphia, PA$21.05–$26.35 / hourThe Research Assistant will support an interdisciplinary research team working primarily on a large, NIH-funded randomized controlled trial studying how teens learn to drive and testing novel interventions to improve driver safety. Depending on study needs, the individual in this position may work 1-3 days per week conducting offsite study visits at CHOP Primary Care Sites or other approved community locations.
Senior Clinical Research Associate ICON PlcSenior Clinical Research AssociateBlue Bell, PARemoteAs a Clinical Research Associate at ICON, you will play a pivotal role in designing and analyzing clinical trials, interpreting complex medical data, and contributing to the advancement of innovative treatments and therapies. Minimum of 1 year independent monitoring to be considered for a Clinical Research Associate II and a minimum of 3 years independent monitoring to be considered for a Senior Clinical Research Associate.
Clinical Research Coordinator - Sr. Thomas Jefferson UniversityClinical Research Coordinator - Sr.Philadelphia, PennsylvaniaJefferson 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 Research Coordinator Sr. Thomas Jefferson UniversityClinical Research Coordinator Sr.Philadelphia, PennsylvaniaWorks independently or with minimal supervision to oversee the day-to-day activities of a clinical trial in accordance with Good Clinical Research Practice (GCP).Runs portions of clinical trials from startup to closeout, including protocol coordination (screening, recruiting, enrolling, consenting), feasibility planning, data management, biological specimen management, preparation for monitoring visits, and regulatory and/or IRB document preparation. 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.