- University of Pennsylvania (Philadelphia, PA)
- …protocols, including accurate data collection and overseeing the quality of the clinical trial data and records, scheduling and conducting study initiation ... Show vigilance in patient safety, protocol compliance and data quality. + Communicate clinical trial patient activity to the investigational drug pharmacy (IDS)… more
- Actalent (Phoenix, AZ)
- …regulations. * Perform vital signs assessments, physical examinations, phlebotomy, and other clinical procedures as required by trial protocols. * Order ... diagnostic tests and liaise with clinical departments and specialists according to the ...and maintain accurate study drug logs and documentation. * Monitor and record patient responses to treatment, adverse events… more
- BeOne Medicines (Emeryville, CA)
- …quality study timelines and tracks progress towards these + Ensures that the clinical studies are operationally feasible, oversees trial feasibility, trial ... Ensures study plans (eg project management plan, monitoring plan, Trial Master File plan, data monitoring plan, ) are...and other stakeholders (including but not limited to regional clinical operations teams and medicator monitor ) +… more
- Actalent (Raleigh, NC)
- … Operations Senior Director. This role requires ensuring successful delivery of clinical trial activities in compliance with Health Authority and regulatory ... a plus. + Experience in prospectively designing and implementing tactics to improve clinical trial execution. Work Environment The work environment offers a… more
- Otsuka America Pharmaceutical Inc. (Annapolis, MD)
- …of assigned trial (s), as assigned.** **Participates in ongoing review of clinical trial data focusing on data integrity, trending and consistency.** ... of programs (eg, Word, Excel, PowerPoint, Outlook, etc.)** **Good understanding of clinical trial related software (eg, eCRFs, IRT, CTMS, etc.).** **Ability… more
- Sanofi Group (Morristown, NJ)
- …pharmacovigilance and clinical operations team + Implements strategies to identify, monitor and resolve clinical program/ trial issues. + Responsible for ... requests and briefing packages for Regulatory agencies, extended synopsis/protocol for clinical trials, Investigator Brochure, Clinical Trial Authorization… more
- Deschutes County (Bend, OR)
- …Health Specialist II (Civil Commitment Investigator/ Monitor ) Print (https://www.governmentjobs.com/careers/deschutes/jobs/newprint/4895689) Apply Behavioral Health ... Specialist II (Civil Commitment Investigator/ Monitor ) Salary $5,851.99 - $8,234.36 Monthly Location Bend, OR...Community Mental Health Program providing safety net and core clinical services for community members in Deschutes County dealing… more
- Actalent (Hackensack, NJ)
- …medical personnel. + Maintain accurate, complete, up-to-date records for each patient in clinical trial protocol. + Ensure appropriate billing for clinical ... research studies. Responsibilities + Assist the principal investigator in preparing proposed clinical trials by reviewing trial protocol and coordinating with… more
- Lilly (IN)
- …external health care professionals according to guidelines above. + Participate in reporting of clinical trial data in Clinical Trial Registry ... and clinical data relevant to the molecule. Clinical Research/ Trial Execution and Support + Plans,...scientific information needs of all investigators and personnel. + Monitor patient safety during the conduct of studies and… more
- BioFire Diagnostics, LLC. (Salt Lake City, UT)
- …the clinical study + Structure, prepare and regularly feed the electronic clinical trial master file, including all the study documentation and main project ... information to competent authorities (EUDAMED, Sunshine act ) + Monitor and report the progress of the above activities...deliverables. + Own the above clinical trial related documentation process Position Requirements:… more