Clinical Research Program Manager C University of PennsylvaniaClinical Research Program Manager CPA$91,066–$117,901 / yearLong-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. The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more.
Scientist Clinical Research Cooper University Health CareScientist Clinical ResearchCamden, NJCompiles, writes and submits project results to principal investigator or Director of Surgical Research.• Confers with industrial, governmental or other groups concerning progress or results of research project. Provide methodological leadership for observational studies, registry analyses, comparative effectiveness research, and real-world evidence studies.•
Clinical Research Associate - Part Time Saint Peter's Healthcare System IncClinical Research Associate - Part TimeNew Brunswick, NJMaintain oversight of designated research project study activities including performing the following functions: Subject recruitment, Consenting and Enrollment/Randomization, Perform study procedures/assessments in accordance with clinical trial guidelines, Complete Data Entry into Case Report Forms and Query Resolution, Process/Ship Specimens per trial requirements, Maintain Regulatory files including delegation logs, FDA form 1572, training logs and other trial documents in compliance with federal and local regulations, Process IRB amendments, annual renewals, closures, etc, Attend regular meetings with members of the project at partnering institutions and sponsors to report on study progress. Initiation / implementation of the observational or clinical research projects assigned including: Maintenance of Investigator and Research Staff CVs, Licensure and Training Records, Drafting and updating the Informed Consent Form with CIRB Boilerplate, Completion of Institutional Review Board (IRB) modifications with supporting documentation.
Clinical Research Coordinator III Rutgers The State University of New JerseyClinical Research Coordinator IIINew Brunswick, NJAligned with Rutgers University-New Brunswick and collaborating university wide, RBHS includes eight schools, a behavioral health network, and six centers and institutes that focus on cancer treatment and research, neuroscience, clinical and translational research, advanced biotechnology and medicine, environmental and occupational health, and health care policy and aging research. Among the key duties of this position are the following: Assist with development and implementation of plans to recruit and retain study participants; assist with interviewing, recruitment and enrollment of human subjects for participation in clinical protocol; distribute and explain processes and goals of clinical studies to participants; assist with development of clinical study informational and educational materials; assist with informed consent process.
Associate Principal Scientist, Clinical Research Merck & Co IncAssociate Principal Scientist, Clinical ResearchWest Point, PA$142,400–$224,100 / yearTranslational Medicine (TMed) drives early clinical development of novel therapeutics by partnering with Discovery Sciences and Late-Stage Clinical Research to translate scientific discoveries into human proof-of-concept and advance the most promising candidates through the pipeline to patients. Leads and directs teams through key study planning, development, and execution activities, including program overviews, issue escalation and mitigation, senior management presentations, cross-functional governance meetings, and advisory meeting preparation.
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 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.
Senior Clinical Research Associate IRESenior Clinical Research AssociatePhiladelphia, PennsylvaniaICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
Clinical Research Coordinator University of PennsylvaniaClinical Research CoordinatorPA$47,313–$50,000 / yearSEES are an essential component of coordinated specialty care for early psychosis and include supporting the young person in exploring interests and goals, navigating educational and employment pathways and programs, pursuing employment opportunities including assistance with job searches, applications, resumes, and interviews, school or training program navigation, and providing support around academic or workplace accommodations. As part of the Department of Psychiatry, Neurodevelopment and Psychosis Division, the Penn Psychosis Evaluation and Recovery Center (PERC) offers consultations on diagnosis, treatment, support and skill development for adolescents and young adults (ages 16-35 years) who exhibit warning signs of emerging psychosis or early psychosis, and their families.
Clinical Research Monitor Actalent IncClinical Research MonitorPhiladelphia, PARemote$40–$50 / hourThe position operates within an academic medical and research environment focused on advanced breast imaging technologies and high-quality interventional breast procedures, including stereotactic, ultrasound-guided, and MRI-guided biopsies. The position centers on risk-based monitoring, Trial Master File (TMF) management, and ensuring adherence to FDA regulations, IND/IDE requirements, and Good Clinical Practice (GCP) guidelines.
Clinical Research Coordinator A/B (OBGYN - PEACE Family Planning) University of PennsylvaniaClinical Research Coordinator A/B (OBGYN - PEACE Family Planning)Philadelphia, PA$47,313–$53,418 / yearLong-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. The University offers a competitive benefits package that includes excellent healthcare and tuition benefits for employees and their families, generous retirement benefits, a wide variety of professional development opportunities, supportive work and family benefits, a wealth of health and wellness programs and resources, and much more.
Marine Field Research Assistant Rutgers The State University of New JerseyMarine Field Research AssistantNew Brunswick, NJUnder the supervision of Dr. Joseph Gradone and Dr. Corday Selden, and in collaboration with an international research team, the Marine Field Research Assistants will support shipboard and field-based scientific operations, including oceanographic sampling, equipment preparation, sample processing, data collection, and general expedition support aboard the research vessel. The Department of Marine and Coastal Sciences seeks to hire two temporary Marine Field Research Assistants to support a Rutgers-led oceanographic research expedition in the Caribbean aboard the R/V Falkor (too) from August 9, 2026, through September 2, 2026, as well as related pre- and post-expedition scientific preparation, logistics, and demobilization activities.
NewClin Research Nurse Manager Temple UniversityClin Research Nurse ManagerPhiladelphia, Pennsylvania$120,000The Clinical Research Nurse Manager in the Lewis Katz School of Medicine's Department of Research Administration will assist the Senior Director, Clinical Research Operations, the Regulatory team and liaise with the various hospital departments in accelerating the start-up, maintenance, and closeout activities of clinical studies, primarily by supporting several clinical research teams for the day-to-day activities surrounding clinical research studies, and will ensure compliance with federal, state and university regulations. *Monitoring and oversight of clinical research staff; observe patient care, and assessing patient status and treatment side effects; maintaining regulatory documentation and managing IRB submissions and follow-ups; and overseeing data collection and management in accordance with trial protocol.
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.
Senior Clinical Research Associate Terumo Medical CorpSenior Clinical Research AssociateSomerset, NJ$92,320–$126,940 / yearSupport the investigator evaluation and recruitment process: o Create phone scripts, questionnaires, and other assessment tools for use in the selection of sites; o Assist team in the development of site recruitment and retention strategy; o Initiate contact with PIs, conduct pre-visits, assess potential investigators and recommend suitability of the site; Assist clinical team with study start-up activities: o Assist in development of protocol / ICF / CRF / CRF completion guidelines, preparation and maintenance of monitoring plans, study binders, study manuals, and other site specific and monitoring tools; o Requests and collects initial regulatory documentation; o Ensure that sites fulfill their regulatory obligations and submit study documents for IRB review and approval; o Performs study tracking and advises PM when an investigational site is approved and ready to receive investigational device supplies; Site Management and study execution activities: o Plan and conduct training / site initiation, interim and close-out visits. Thorough understanding of operational aspects of clinical research and regulatory regulations; Good interpersonal, problem solving and communication skills; Excellent follow-through capability; Self-motivated, attention to detail and organizational skill; Experience with various computer systems / applications and clinical trial management systems; willingness to learn new systems / databases as needed.
Supervising Advanced Practice Nurse (Cell Therapy Research) Rutgers The State University of New JerseySupervising Advanced Practice Nurse (Cell Therapy Research)New Brunswick, NJMISSION: Our mission is to accelerate scientific discovery focused on understanding cancer, innovating cancer treatment, and improving cancer prevention; to provide outstanding, novel, and compassionate patient care; to provide evidence-based and culturally informed education to physicians, nurses, researchers, staff, and the community; and to achieve cancer health equity in our state through outreach to and engagement of our extraordinarily diverse communities. The primary purpose of the Supervising Advanced Practice Nurse of Cell Therapy Research is to provide day business administrative leadership and clinical management of assigned areas through skillful directing, coaching, support, and delegation to research staff in the provision of clinically safe, fiscally sound, compassionate care and services.
Clinical Research Nurse-D University of PennsylvaniaClinical Research Nurse-DPhiladelphia, PA$75,804–$99,818 / yearAct in lead capacity in coordination of CRU projects and assist CRU managers in overseeing execution of project timelines as well as completion of study related activities delegated to research coordinator who provides study related support. Triage any questions participants may have regarding protocol specifics, investigational products, lab results, effects of therapies, medications, and symptom management within clinical scope and level of expertise and referring other questions to the PI or medical team in order to obtain guidance or assistance.
FSP Sr. Clinical Research Associate II - NYC Metro or PHL - Onc Fortrea IncFSP Sr. Clinical Research Associate II - NYC Metro or PHL - OncTrenton, NJRemote$125,000–$140,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
NewFSP Clinical Research Associate 2 Fortrea IncFSP Clinical Research Associate 2NJRemote$100,000–$112,000 / yearResponsibilities: Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -. Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data.
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.