- Merck (North Wales, PA)
- …stakeholders (eg, study team, country teams, vendors, committees) in support of clinical study objectives. + Accountable for managing any study specific ... study planning, development, and execution elements (eg, data management deliverables, trial level plans/timelines, country/site selection, site materials, system… more
- CSL Behring (King Of Prussia, PA)
- …(CTS) Senior Study Manager manages the end-to-end supply chain for assigned clinical studies throughout the multi-year study lifecycle. The CTS Senior ... Study Manager independently leads clinical studies to ensure compliant,...supply plans. + Specifies ancillaries supplies with input from Clinical Development Operations, Clinical Science … more
- Actalent (Philadelphia, PA)
- Job Title: Senior Clinical Study ManagerJob Description The Senior Clinical Study Manager will be responsible for ensuring the delivery and execution of ... clinical studies in one or more geographic...execution. Key responsibilities include leading the development of the clinical study plan, managing study … more
- Bristol Myers Squibb (Princeton, NJ)
- …Clinical Trial Package (CTP) regulatory documents for site activation and ongoing study management .t + When applicable, conduct drug/IMP label review & ... activities related to study start-up and ongoing study document management . + Act as point...to trial milestones. + Prepare Investigator Sites to conduct clinical trials through the review and approval of essential… more
- Merck (North Wales, PA)
- …in a clinical trial environment. + MS (preferred) in Computer Science , Statistics, Applied Mathematics, Life Sciences, Engineering or related field with a ... & Development (R&D) projects (data, analyses, tables, graphics, listings). + Clinical Data Interchange Standards Consortium (CDISC), Study Data Tabulation… more
- Novo Nordisk (Plainsboro, NJ)
- …to make a difference? The Position The Novo Nordisk Real World Evidence (RWE) / Clinical Data Science & Evidence (CDSE) - Fellow is responsible for supporting ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...and execution of observational research / Real World Evidence studies to support the Evidence and Insights Generation Plans… more
- University of Pennsylvania (Philadelphia, PA)
- …resources, and much more. Posted Job Title Nurse Practitioner (The Center for Studies of Addiction - CSA) Job Profile Title Nurse Practitioner Job Description ... Summary The Center for Studies of Addiction (CSA) seeks an energetic Nurse Practitioner...conduct physical examinations, make diagnoses, provide medical detoxification, conduct study visits, and counsel individuals in the treatment and… more
- University of Pennsylvania (Philadelphia, PA)
- … visits and regulatory compliance in one or more studies . Clinical Research Coordinator work includes study design, protocol development, submission to ... the understanding and assessing potential treatments for Williams Syndrome. Clinical Research Coordinator work includes study design,... visits and regulatory compliance in one or more studies . This position is responsible for study … more
- University of Pennsylvania (Philadelphia, PA)
- … clinical research studies , including the recruitment and retention of clinical trial participants. Schedules and runs study visits as per protocol. ... the monitoring of external sites and assists in the management of multi site trials. CRC-B: This is an... studies , including the recruitment and retention of clinical trial participants. Schedules and runs study … more
- University of Pennsylvania (Philadelphia, PA)
- …join a group of research staff that support clinical AI and data science research, including ongoing investigator-initiated studies and new studies that ... observational and retrospective studies , and include single-site and multi-site studies . Clinical Research Coordinator A: Coordinate Phase 0-III clinical… more
- University of Pennsylvania (Philadelphia, PA)
- …is required. Job Description Job Responsibilities + Coordinate and conduct clinical studies , includes; subject recruitment, informed consent, chart maintenance ... Job Description Summary This position will assist in the management of multiple clinical trials and responsibilities...federal regulations and guidance documents for the conduct of clinical studies and human subject protection +… more
- University of Pennsylvania (Philadelphia, PA)
- …all University of Pennsylvania, IND, and GCP guidelines by all personnel involved in clinical studies . + Assist in the preparation and submission of regulatory ... other relevant bodies, and may supervise other lab members in clinical study -related activities. Effective problem-solving abilities; effective communication and… more
- Pfizer (Collegeville, PA)
- …development and translation of clinical research plans into efficiently delivered studies . Creative in the conception of novel study designs and collaborates ... pivotal role in the ideation and maturation of leading-edge clinical science applied to drug development. **ROLE...experience. + Ability to design, initiate and conduct effective clinical studies applying novel principles as appropriate,… more
- Bristol Myers Squibb (Princeton, NJ)
- …in partnership with the Clinical Trial Leads (CTLs) for study -related medical questions and education (including safety management guidelines). Provides ... affairs-led sponsored studies (interventional and non-interventional), Investigators Sponsored Studies (ISRs) and Clinical Research Collaborations (CRCs), in… more
- University of Pennsylvania (Philadelphia, PA)
- …The mission of the ACC Clinical Research Unit (CRU) is to advance the science of cancer care, serve our patients by improving clinical outcomes, and offer ... the ACC. Job Description The Leukemia Research Team seeks a full-time, registered Clinical Research Nurse (CRN) to conduct studies involving a wide variety… more
- University of Pennsylvania (Philadelphia, PA)
- …enrollment, study visits and regulatory compliance in one or more studies . Job Description Research coordinator work includes study implementation, document ... visits and regulatory compliance in one or more studies . Duties: Clinical ResearchCoordinator B: Participate in...Work directly with investigators to design, set-up and execute studies . Accountable for making sure study timelines… more
- University of Pennsylvania (Philadelphia, PA)
- …of the CRC-A include recruitment and enrollment; data collection, entry, and management in accordance with study protocols; organizing and maintaining the ... of the CRC-A include recruitment and enrollment; data collection, entry, and management in accordance with study protocols; organizing and maintaining the… more
- Penn Medicine (Philadelphia, PA)
- …O. Dickens Center for Women's Health patients are screened for eligibility for opened clinical studies . They are responsible for detailed data entry, training of ... submission to the IRB (local, CIRB). Participates in the development/ management of study budgets. Manages and maintains...products, lab results, effects of therapies, medications, and symptom management within clinical scope and level of… more
- University of Pennsylvania (Philadelphia, PA)
- …The mission of the ACC Clinical Research Unit (CRU) is to advance the science of cancer care, serve our patients by improving clinical outcomes, and offer ... Related Diseases ("Program") of the University of Pennsylvania seeks a full-time, registered Clinical Research Nurse C/D to conduct studies involving a wide… more
- University of Pennsylvania (Philadelphia, PA)
- …in preparation of manuscripts and research related presentations. Responsible for study coordination for investigator-initiated studies , multi-center research ... patient-oriented research projects. Job Description Participate in and coordinate patient-oriented clinical and translational studies within the University of… more