- MVP Health Care (Rochester, NY)
- …thinking and continuous improvement. To achieve this, we're looking for an ** Associate , Post-Acute Clinical Support Specialist** to join #TeamMVP. If you ... + Work closely with internal and external stakeholders to support clinical documentation, ensuring accuracy and compliance with organizational and regulatory… more
- Touro University (New York, NY)
- …invites applications for a full-time position at the rank of Assistant or Associate Professor in Clinical Mental Health Counseling. Position is effective July ... Responsibilities include but are not limited to: + Teach full-time graduate-level Clinical Mental Health Counseling courses (3-3). + Advise ongoing load of CMHC… more
- Takeda Pharmaceuticals (Boston, MA)
- …**Job Description** **OBJECTIVES:** + Provides oversight from a clinical research and pharmacovigilance perspective of regulated post-authorization activities ... units and the affiliate and enables them to deliver their clinical research and pharmacovigilance-related regulated activities with high compliance and agility.… more
- CTTX Health (Cambridge, MA)
- …and ready to make an impact on patients' lives? We're looking for a Clinical Research Associate (CRA) to join a fast-growing biotech company (confidential) ... ensure trials meet the highest quality standards. + Review and verify study data for accuracy and completeness. + Collaborate with site staff and cross-functional… more
- ThermoFisher Scientific (Chicago, IL)
- …weather conditions **Job Description** Performs and coordinates all aspects of the clinical monitoring and site management process. Conducts remote or on-site visits ... regulations and SOPs to guarantee subjects rights, well-being and data reliability. Ensures audit readiness. Develops collaborative relationships with… more
- SUNY Upstate Medical University (Syracuse, NY)
- Job Summary: Position is Project Manager for a large multi-site clinical trial. Train and oversee CRA's on the project. Clinical Site is also Coordination Center ... clinical trial. Manage all aspects of the clinical trial at the Sponsor Level including but not...selection, consent form development, study document creation, study and data monitoring oversight, SAE and protocol deviation reporting and… more
- SUNY Upstate Medical University (Syracuse, NY)
- …and ship lab samples, schedule and conduct follow up research appointments for clinical trial participants, data collection and entry into paper and electronic ... Job Summary: This position is responsible for the coordination of ALS clinical research studies. Performance of regulatory tasks including IRB and sponsor/CRO… more
- UTMB Health (Beeville, TX)
- Correctional Clinical Associate (CCA) - Mcconnell Unit **Beeville, Texas, United States** Clerical & Administrative Support UTMB Health Requisition # 2504386 The ... Functions: + Operates personal computers to enter and assimilate data , generate reports, draft routine correspondence, and develop special administrative… more
- ThermoFisher Scientific (Austin, TX)
- …actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site ... approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May… more
- ThermoFisher Scientific (Chicago, IL)
- …actions to bring the site into compliance and decrease risks. Ensures data accuracy through SDR, SDV and CRF review as applicable through on-site ... approved business writing standards. Escalates observed deficiencies and issues to clinical management expeditiously and follow all issues through to resolution. May… more