- BeiGene (Emeryville, CA)
- **General Description:** + Responsible for the delivery of study start -up, initial and ongoing submissions within established timelines with high quality and in ... on potential first site(s) to be selected/activated to achieve FPI. + Site Start -Up + Skilled in driving kick-off and completion of tasks from selection through… more
- ConvaTec (Lexington, MA)
- …for nothing short of excellence. Join us on our journey to #ForeverCaring as a Clinical Study Management Specialist , and you'll do the same. **About the ... operational aspects including: budgets, timelines, resources, CRO/vendor selection. Oversee clinical team staff during study start...and authority:** + Proactively manage assigned clinical studies . + Support clinical study … more
- University of Colorado (Aurora, CO)
- Clinical Research Startup Specialist - 33101...for all activities related to the successful conduct of clinical research, from study start -up ... Research Support Team (CReST) - OVCR** **Job Title: Clinical Research Startup Specialist ** **Position #: 00821154...for all activities related to the successful conduct of clinical research, from study start -up… more
- Johns Hopkins University (Baltimore, MD)
- …accuracy. + Complete IRB amendment submissions and ensure documentation of training. + Attend study start up meeting for studies including those where SKCCC ... as Greater Than One (GTO), coordination and management of clinical studies with JHU and 4 collaborating...all trials within the program. + Review and analyze studies for difficulties that may arise with study… more
- Stanford University (Stanford, CA)
- …be responsible for the management of virtual and multisite operations by ensuring adequate study start up, regulatory submissions and training of each of the ... Clinical Research Operations Specialist II (REACT)...ability to give presentations to stakeholders. + Knowledge of Clinical Research Study Startup processes including IRB… more
- Beth Israel Lahey Health (Burlington, MA)
- …States of America) **Job Description:** **Position Summary:** Coordinates multiple research studies by implementing study protocols in accordance regulatory and ... & Responsibilities** _including but not limited to:_ Implements assigned research studies by reviewing study and assessing institutional requirements: Implements… more
- Banner Health (Loveland, CO)
- …patient and staff education, multidisciplinary team involvement with finance, regulatory, study start up, on-site coordination, principal investigators, as well ... advances and caring attention to patient needs. As an **Oncology Research Clinical Pharmacy Specialist ,** you will investigate product management, sponsor… more
- Actalent (Hackensack, NJ)
- …and effectively communicates these updates at weekly division meetings to the clinical study teams and Principal Investigators. + Effectively communicates with ... IMMEDIATE SITE START UP SPECIALIST WITH LEADING ONCOLOGY... Staff and Ancillary Department Review/Approvals. + Regularly update Clinical Trial Management System on Start Up… more
- Kelly Services (Phoenix, AZ)
- ** Clinical Product Quality Specialist ** Kelly Science and ...Monday to Friday, 8:00 am to 5:00 pm (Flexibility to start at 6 am depending on study needs ... 8-hour shifts) **Reporting To** : Quality Assurance Director **Position Summary:** The Clinical QA Specialist is responsible for administering routine quality… more
- Veterans Affairs, Veterans Health Administration (Hampton, VA)
- …(HIM) section at the Hampton VA Medical Center. The Medical Records Technician ( Clinical Documentation Improvement Specialist (CDIS) - Inpatient) is skilled in ... include: Clinical Documentation Improvement Practitioner (CDIP) & Certified Clinical Documentation Specialist (CCDS). You must also demonstrate the… more
- Veterans Affairs, Veterans Health Administration (Temple, TX)
- …Central Texas Veterans Health Care System. The Medical Records Technician- Clinical Documentation Improvement Specialist (Outpatient/Inpatient) is responsible for ... met when determining the grade of candidates: Medical Records Technician- Clinical Documentation Improvement Specialist (Outpatient/Inpatient), GS-09 (Full… more
- The County of Los Angeles (Los Angeles, CA)
- CLINICAL NURSE SPECIALIST (VARIOUS SPECIALTIES) Print (https://www.governmentjobs.com/careers/lacounty/jobs/newprint/1143342) Apply CLINICAL NURSE ... the person is qualified to use the title of Clinical Nurse Specialist , both issued by the...be a violation of the Use Disclaimer. Test Preparation: Study Guides and other resources are available to help… more
- Actalent (Hackensack, NJ)
- …for Physician, Study Staff and Ancillary Department Review/Approvals. Regularly update Clinical Trial Management System on Start Up progress and effectively ... communicates these updates at weekly division meetings to the clinical study teams and Principal Investigators. Effectively communicates with the budget &… more
- University of Washington (Seattle, WA)
- …CTO review workflows. * Determine appropriate workflow pathway for proper routing of studies through the start -up process. * Perform Pre-CTO Admin Tasks import ... process for study submissions. * Perform Pre-Activation Checks for ...the CTO Database (CTODB), Epic, and other comprehensive electronic study documentation for each clinical research … more
- ConvaTec (Cleveland, OH)
- …through coordination of clinical programs and product education inclusive of clinical study /paper reviews with the field sales team, as cross-functional ... more about Convatec, please visit http://www.convatecgroup.com **About the role:** As the Ostomy Clinical Resource Specialist based in Ohio, you will play a… more
- Harvard University (Cambridge, MA)
- …conditions, or any other characteristic protected by law.Job Summary: The Clinical Implementation Specialist will report to the Assistant Director ... The Specialist will leverage managerial experiences and expertise in clinical settings to foster relationships between Ariadne Labs and the leaders and… more
- Veterans Affairs, Veterans Health Administration (Santa Rosa, CA)
- …with prescribing privileges as outlined in the individual's scope of practice for the Clinical Pharmacy Specialist (CPS) in Mental Health as part of the ... on their team. Responsibilities VA Careers - Pharmacy: https://youtube.com/embed/Fn\_ickNBEws Clinical - Direct Patient Care Activities that require a scope… more
- Actalent (Philadelphia, PA)
- …of the new study , as well as, communicate transition of the new study to the applicable team Regulatory Affairs Specialist post-site initiation Skills: irb, ... regulatory, submission, adverse events, Clinical research, gcp, regulatory submission, oncology, Clinical ...events, Clinical research, gcp, regulatory submission, oncology, Clinical trial, consent form Top Skills Details: irb, regulatory,… more
- Veterans Affairs, Veterans Health Administration (Walla Walla, WA)
- …Center in Walla Walla, Washington. The incumbent will serve as a Health System Specialist (Executive assistant) to the Chief of Staff (COS). The incumbent serves as ... long-and short-range plans and programs. Responsibilities Duties of the Health System Specialist (Executive Assistant) include but are not limited to the following:… more
- University of Pennsylvania (Philadelphia, PA)
- …objectives, with close supervision. Assists in performing laboratory experiments and clinical studies for product or material formulation and development. ... red blood cell disorders, is looking for a Research Specialist A to start in spring/summer 2024....with 0-1 years of related experience in research and clinical study methodologies or equivalent combination of… more