- Actalent (Remote, OR)
- …Job Description We are seeking a dedicated Trial Disclosure Associate to support clinical trial applications through the Clinical Trial Information ... functional areas to meet project objectives. Responsibilities + Support clinical trial applications via CTIS by uploading...+ Track CTIS application details to compile metrics and monitor notifications, due dates, and trends. + Identify system… more
- Dana-Farber Cancer Institute (Brookline, MA)
- The Data Integrity / Clinical Trials Billing Specialist performs charge validation through account review in a timely and billing compliant manner. The Data ... Integrity / Clinical Trials Billing Specialist will develop a mastery of...England states (ME, NH, VT, MA, RI, CT) + Monitor and resolve charging issues within Account, Claim Edit,… more
- Amgen (Thousand Oaks, CA)
- … Practices (GCPs), FDA regulations, quality assurance and pharmaceutical industry; 3. Clinical trial processes and operations; 4. Knowledge of ICH/GCP ... timelines; 7. Time, cost, and quality metrics, Key performance Indicators (KPIs); 8. Clinical Trial Management Systems like Medidata or Veeva, and Interactive… more
- University of Southern California (San Diego, CA)
- …hires, and supervises clinical monitors + Responsible for all clinical monitor training and ongoing clinical trial education for monitors + ... Clinical Monitor Line ManagerApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/San-Diego-CA/ Clinical - Monitor… more
- Robert Half Office Team (Lewiston, ME)
- …and billing functions as part of the role. * Participate in clinical trial operations as required. * Monitor patient accounts and take necessary actions ... based on account status. Requirements Qualifications: + HS Diploma or GED required + Previous experience in a customer-facing role (retail, hospitality, call center, etc.) + Strong communication and problem-solving skills + Ability to multitask in a fast-paced… more
- Children's Hospital Los Angeles (Los Angeles, CA)
- …guidelines governing the protection of human research subjects. * Experience using Clinical Trial Management Systems (CTMS) and Electronic Medical Records (EMR). ... rewarding. **It's Work That Matters.** **Overview** **Purpose Statement/Position Summary:** The Clinical Research Monitor Sr. serves as a senior-level… more
- Amgen (Washington, DC)
- … expert in translational and clinical oncology + Collaborate with medical monitor to support clinical trial level activities + Present information ... approval. + Provide clinical input into & implementation of clinical trial (s), their delivery, clinical data review, interpretation of results. Review… more
- ThermoFisher Scientific (Bohemia, NY)
- …and meet quality and construction specifications as defined by the Clinical Trial Industry and cGMP standards. Monitor and trouble shoot operations during ... proprietary translation and regulatory approval system are invented to reduce overall clinical trial label cycle times. **How Will You Make an Impact?** Builds… more
- Johns Hopkins University (Baltimore, MD)
- …with collaborating 20+ clinical sites across the country in support of clinical trial research goals. Activities include training and managing clinical ... and performance plans, assign tasks and deadlines to site clinical teams, direct and monitor clinical...Abilities** + Understanding and ability to apply knowledge of clinical trial designs to trial … more
- Georgetown Univerisity (Washington, DC)
- …regulatory maintenance, adherence with ongoing training requirements, accurate reporting of clinical trial visits via the OnCore/CTMS system, accurate and ... adverse events, and timely communication with team members and clinical trial sponsors. + Coordinate 7 migraine/headache,..., and to the sponsor contact (eg, the study monitor appointed by the sponsor for each trial… more