- Green Line Talent Group (New Haven, CT)
- About the job Senior Clinical Trial / Clinical Trial Project Manager Senior Clinical Trial Project Manager / Clinical Trial Project Manager ... We are seeking a highly organized and dynamic Senior Clinical Trial Project Manager/ Clinical ... trials spanning 4070 sites and approximately 500 subjects. Monitor CRO performance, ensuring adherence to timelines, budgets, and… more
- Eli Lilly and Company (Indianapolis, IN)
- …to make life better for people around the world. Purpose: The Associate Director, Clinical Trial Foundations (CTF), will serve as the subject matter expert for ... clinical systems and capabilities supporting clinical development....and training. Develop critical success factors for pilots/projects and monitor progress to ensure clear criteria exists to enable… more
- Merck & Co. (Rahway, NJ)
- …execution of clinical protocol(s) . This may include: Serving as the lead clinical scientist on the clinical trial team. Leading medical monitoring team ... the protocol in collaboration with Data Management/Programming. Collaborating cross-functionally to monitor clinical data -to ensure quality, completeness , and… more
- Merck & Co. (Rahway, NJ)
- …execution of clinical protocol(s). This may include:Serving as the lead clinical scientist on the clinical trial team.Leading medical monitoring ... the protocol in collaboration with Data Management/Programming.Collaborating cross-functionally to monitor clinical data to ensure quality, completeness, and… more
- Eisai, Inc (Nutley, NJ)
- …Operations is a senior leadership role responsible for overseeing all aspects of clinical trial execution within a pharmaceutical or biotechnology company. This ... This role requires a deep understanding of the entire clinical trial process, from initial planning and...other stakeholders to ensure alignment and successful execution of clinical trials. Monitor study progress, identifying and mitigating… more
- Dana-Farber Cancer Institute (Boston, MA)
- …Research Nursing, and other departments, as needed per the requirements of the clinical trial . Responsible for organizing and preparing for both internal and ... Responsible for data entry of Subject Visit Tracking information into Clinical Trial Management System contemporaneously with medical visits, assessments,… more
- Hackensack Meridian Health (Paramus, NJ)
- …and works under the general supervision of the principal investigator responsible for the clinical trial (s) to which is assigned. Responsibilities A day in the ... on each protocol and each patient participating in a clinical trial protocol in the clinical...appropriately. Schedules, coordinates, prepares, and assists for all sponsor monitor site visits and ensures all supporting documentation records… more
- START Center for Cancer Research (San Antonio, TX)
- …of patients who are treated in community practices and hospitals without access to a clinical trial when their care journey calls for one. START serves the many ... largest roster of Principal Investigators (PIs) across its eight clinical trial sites. Committed to accelerating passage...questions, concerns, as well as status of the protocol. Monitor the overall day-to-day conduct of assigned studies in… more
- Altasciences (Cypress, CA)
- …Practical Nurse to play a vital role in safeguarding the wellbeing of clinical trial participants and supporting the highest standards of operational excellence. ... mentor to Clinical Operations team members. Ensure the confidentiality of clinical trial participants and sponsors is respected. Continuously assess safety… more
- University of Kansas Medical Center (Kansas City, KS)
- …absence and all other duties assigned by supervisor. Prepare documentation for clinical trial feasibility and site qualification visits. Assist with protocol ... activities involved in the collection, compilation, documentation, and analysis of clinical research data. Monitor participants' progress including documenting… more
- Eli Lilly and Company (Indianapolis, IN)
- …product development activities over the entire spectrum of drug development and clinical trial phases. Specific activities include developing or contributing to ... of phase 3b/4 studies , as well as non clinical trial solutions/activities that are conducted in...the scientific information needs of all investigators and personnel. Monitor patient safety during the conduct of studies and… more
- The University of Pennsylvania (Philadelphia, PA)
- …CRU that requires RN involvement, will directly report to the Director of Clinical Research, collaborate with study teams, monitor , document, and educate adverse ... health and wellness programs and resources, and much more. Posted Job Title Clinical Research Nurse C/D (Department of Radiation Oncology) Job Profile Title … more
- Kailera Therapeutics, Inc. (Waltham, MA)
- …or hybrid 2-3 days per week). Responsibilities: Provide project-level leadership for clinical data management (CDM) activities, monitor and report on overall ... join our team. What You'll Do: The Associate Director, Clinical Data Management plays a key role within the...to data quality and ensuring appropriate filing in the Trial Master File (eTMF) Manage CRO CDM counterparts to… more
- CryoLife (Kennesaw, GA)
- …contact between the sponsor, investigational sites, and other stakeholders involved in the clinical trial . Prepare and review on-site files and records, case ... our website, www.artivion.com. Position Objective: To independently manage and monitor all aspects of clinical trials at...protocol and all GCP procedures. Oversee the execution of clinical trial protocol. Participate in the execution… more
- Children's National Hospital (Washington, DC)
- …regulations, data access rules, and privacy regulations, as necessary. Ensure that clinical trial projects are properly resourced, managed and executed within ... analyzing data to support upper management decision-making. Ensure compliance and monitor performance of investigational sites/subcontracts for clinical studies;… more
- Cedars Sinai (West Hollywood, CA)
- …and Safety Letters in accordance with local and federal guidelines. Assists with clinical trial budgets and patient research billing. Responsible for sample ... are maintained in association with the triad of accurate longitudinal clinical metadata, comprehensive genotype information and serotypes. These resources are made… more
- Medpace, Inc. (Cincinnati, OH)
- …communicate/present both virtuall and face to face; and Support collaboration with Clinical Trial Manager other functional areas to provide study deliverables. ... Job Summary Our Clinical Packaging & Supplies team is growing rapidly,...chain, potentially including manufacturing, packaging, labeling, storage, and distribution; Monitor alignment of CP&S timelines with project timelines; Attend… more
- Arrowhead Pharmaceuticals (San Diego, CA)
- …Requirements: 2 years in clinical research 2 years as a Clinical Trial Associate; study coordinator Proficient knowledge and understanding of ICH-GCP ... Arrowhead Pharmaceuticals, Inc. (Nasdaq: ARWR) is a clinical stage biopharmaceutical company that develops medicines that treat intractable diseases by silencing the… more
- Cedars Sinai (Los Angeles, CA)
- …available for this position at this time. This position functions as a Clinical Research Coordinator providing support for clinical research protocols for the ... Coordinator will assist the Research Department with all aspects of clinical research. This individual will interact with principal investigators, subjects, clinic… more
- BioSpace (New York, NY)
- …conferences, scientific workshops, and review of key publications and resources. Support clinical trial execution, including recruitment and site outreach, as ... institutional leaders, medical groups, and consortia. Provide scientific evidence and clinical trial information to healthcare professionals, clinical … more
