- Regeneron Pharmaceuticals (Cambridge, MA)
- We are seeking an ** Associate Director- Clinical Trial Management** to join our Oncology team as a part of our new Regeneron Cell Medicines (RCM) group. You ... identification of project risks and contingency planning. **As an Associate Director- Clinical Trial Management,...study managers, field clinical monitors, and investigative site staff to ensure trial (s) are managed… more
- Bristol Myers Squibb (Princeton, NJ)
- … Clinical Research or related work + Experience in the use of industry Clinical Trial Management Systems + Additional complex software application related to ... and non-drug (Lab kits, ECG) importation to support study site + Complete all payment activities including preparing invoices,...clinical trial research (ie electronic data capture… more
- University of Utah (Salt Lake City, UT)
- …City, UT **Track** **New Position to Begin** As soon as possible **Details** ** CLINICAL TRIAL AND TRANSLATIONAL RESEARCH , BREAST MEDICAL ONCOLOGY** **Huntsman ... post-doctoral training; 2) Must have an established track record of clinical trial leadership/enrollment and scientific accomplishments with extramural industry… more
- Amgen (Washington, DC)
- …your best work alongside other innovative, driven professionals in this meaningful role. ** Clinical Trial Oversight Manager** **Live** **What you will do** Let's ... experience OR + Bachelor's degree & 5 years of clinical experience OR + Associate 's degree &...medically related field + 4 years' experience working in clinical site management (working on clinical… more
- Merck (Philadelphia, PA)
- …strategic direction, and overall performance of the eSSC. Ensures sound clinical development principles are incorporated into the services provided by the ... improvement efforts. + Serve as POC during sponsor and site inspections related to services within the eSSC. +...experience in people management and/or team leadership OR + Associate degree with 14 years' experience in people management… more
- Cedars-Sinai (Los Angeles, CA)
- …care the most. **Req ID** : 199 **Working Title** : Clinical Research Associate I - Lung Institute Biobank (On- Site ) **Department** : Research - Pulmonary ... for high quality basic and translational research. As a Clinical Research Associate I, you will work...accordance with local and federal guidelines. + Assists with clinical trial budgets. + Assists with patient… more
- Abbott (Santa Clara, CA)
- …or Maple Grove, MN currently has an on- site opportunity for an ** Associate Director, Clinical Safety** professional. Reporting to the Global Safety Director, ... and procedures. + Oversight of the staff that perform the day-to-day clinical trial adverse event processing function and serious adverse events reporting to… more
- University of Colorado (Aurora, CO)
- Associate Director or Director of Clinical ...site teams and other stakeholders on phase 1 clinical trial protocols and standardized processes. + ... and manage long- and short-term strategic planning in direct support of ongoing clinical trial advancements and operations. + Manage strategic staffing for … more
- Taiho Oncology (Princeton, NJ)
- …of timelines, budget, recruitment and country/ site selection strategies, and provision of clinical trial materials. + Serves as main study contact for the ... Associate Director, Clinical Operations Pleasanton, CA,...sites. + Responsible for the financial management of the clinical trial in conjunction with his/her supervisor… more
- Novo Nordisk (Washington, DC)
- …of clinical trials and improvement/innovation projects for NACD and Novo Nordisk (eg, clinical trial site staff, clinical research vendors). Manages ... Development (NACD) goals, including successful delivery of studies within the clinical trial portfolio. Contributes to local or increasingly complex… more
- AbbVie (North Chicago, IL)
- …electronic document conventions and processes consistently and accurately. + Integrate clinical trial data across studies, identify issues impacting projects ... Job Description This position will be required to be on- site 3 days / week from our Lake County,...office + Prepare scientific reports and presentations related to clinical trials using available software and templates. + Reviews… more
- Catalyst Clinical Research LLC (Raleigh, NC)
- …Project Manager. + Internal support is provided to the Field Monitor from the assigned Clinical Trial Associate . + Works closely with the extended study team ... Job Duties: As a Senior Clinical Research Associate , you will monitor clinical trial...and working practices. You will collaborate with an assigned clinical research team to provide input on site… more
- ThermoFisher Scientific (Columbus, OH)
- … clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy ... Impactful Work:** Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts...study systems are updated per agreed study conventions (eg Clinical Trial Management System, CTMS). Performs QC… more
- Abbott (Atlanta, GA)
- …sites and other Abbott clinical staff (eg, operations management, study team, Site Contracts Associate ), as needed. **Manage all aspects of study lifecycle ... (as needed), procedure outcomes and early indication of trends, clinical trial enrollment, and ICH-GCP and ...appropriate collaboration with Abbott clinical staff, eg Site CRA, Site Contract Associate .… more
- Bristol Myers Squibb (Brisbane, CA)
- …Summary / Objective** + Responsible for implementation, planning, and execution of assigned clinical trial activities. Serves as Clinical Trial ... team members + May support clinical development planning (collaboration with Clinical Development Lead/ Clinical Trial Physician for provision and… more
- Edwards Lifesciences (Columbus, OH)
- …Edwards Tricuspid team based in the Midwest region. As the Associate Clinical Research Monitor, you will ensure trial patients' safety by assuring trials ... for consistency with case report form, and determine if clinical trial /study subject documentation is within parameters...preferred + Ability to travel up to 75% for clinical site visits + Covid Vaccination **What… more
- Taiho Oncology (Pleasanton, CA)
- Study Associate I, Clinical Operations Pleasanton, CA,...Knowledge, Skills, and Abilities: + 2 years of relevant clinical trial support or site ... Must possess the ability to multi-task and effectively prioritize in order to ensure clinical trial goals. + Recognize potential obstacles and work to resolve… more
- BeiGene (Emeryville, CA)
- …Oversees the administration of invoice reconciliation, scoping, and change orders, for clinical trial operations **Planning/Leading:** + Supports COM with ... The Associate Director (AD) Clinical Study Management leads both...clinical trial management; ensures that clinical trials are operationally feasible… more
- Actalent (Basking Ridge, NJ)
- …and International Conference on Harmonization (ICH) guidelines. * Key focus is on providing clinical trial management support to study teams and tracking CRO and ... the supervision of the Study Manager role the Study Associate Manager within Clinical Operations, in adherence... system, Clinical project management, cro, irb, clinical study, regulatory documents, clinical trial… more
- Abbott (Alameda, CA)
- …and experiences required. + Must have 3+ years of relevant experience in site monitoring, clinical trial practices and regulations. **Preferred ... the study to cross functional teams. + Perform study site visits (SQV, SIV, IMV, COV), ensuring compliance to...management. + Solid understanding and demonstrated experience of the clinical trial process including study design and… more