- Astrix Technology (Fort Worth, TX)
- **Technical Documentation Specialist II ** Clinical Fort Worth, TX, US Pay Rate Low: 30.00 | Pay Rate High: 42.00 + Added - 25/11/2024 Apply for Job Exciting ... world - with complementary businesses in Surgical and Vision Care. Technical Documentation Specialist II Fort Worth, TX (Onsite) 24 months $35.00-$42.00 +… more
- Cedars-Sinai (Los Angeles, CA)
- …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board . Primary Duties & Responsibilities + May ... nationally for excellence in research!** The Clinical Research Data Specialist II manages the data for assigned...including the Food and Drug Administration (FDA) and local Institutional Review Board + Maintains… more
- University of Rochester (Rochester, NY)
- …University of Rochester is seeking a part-time (20 hours/week) Human Subject Research Specialist , Level II , to coordinate human subject research activities. The ... participant adherence with protocol requirements. - Participates in the development, review and approval of case report forms (CRFs) and study-specific procedure… more
- University of Rochester (Rochester, NY)
- …individual, and internal equity considerations._ **Responsibilities:** The Neurology Study Coordinator II - CNRG will work within the Department of Neurology's ... clinical trials, and multi-center clinical research studies. The Study Coordinator II will have considerable latitude for independent judgment and coordinates all… more
- Mount Sinai Health System (New York, NY)
- …to the appropriate committee ( Institutional Animal Care and Use Committee, Institutional Review Board , Bio-Safety Officer and Financial Conflict of ... experience. + Clinical trials negotiation training (MAGI, etc.) desirable. + Certified IRB Professional (CIP): Active Certification -- or Eligibility to take the… more
- University of Rochester (Rochester, NY)
- …at The University of Rochester is seeking a full-time Human Subject Research Specialist , Level II , to coordinate human subject research activities. The division ... subject studies. May provide training on federal, state, sponsor and/or institutional regulations, policies and practices related to human subject research.… more
- Stanford University (Stanford, CA)
- …the development phase, including draft content and formatting to meet requirements of Stanford, Institutional Review Board ( IRB ), United States Food and ... patients worldwide. BMT-CT is seeking a Clinical Trials Regulatory II Specialist to support a very active...+ Strong knowledge of regulatory affairs, including FDA regulations, IRB review and approval process, and Good… more
- Methodist Health System (Dallas, TX)
- …the IRB . * Create and/or adapt clinical trial informed consent documents for Institutional Review Board ( IRB ) submission. * Maintain regulatory ... Shift :** **Job Description :** Your Job: The Regulatory Specialist will perform expertise in the regulatory component of...research trials to include, but not limited to; Phase II and IV clinical, investigator initiated trials (IITs), and… more
- Johns Hopkins University (Baltimore, MD)
- …implement systems to decrease delay in the approval process. + Assists the Start Up Specialist with new study IRB submissions as needed. + Ensures smooth study ... the Program Manager in GU Oncology Programs. The Sr. Research Program Coordinator II will work under minimal supervision and will be responsible for ensuring that… more
- Beth Israel Lahey Health (Burlington, MA)
- …Drug Enforcement Administration. Maintains certification and credentials in accordance with the Board of Registration and adheres to institutional policies and ... signing bonus eligible jobs and amounts at any time. Pharmacy Specialist /Senior Clinical Pharmacist Emergency Medicine- 7on/7off evenings. This position will work… more
- Pennsylvania State University (Hershey, PA)
- …protocols under physician investigator guidance and delegation and clinical research specialist and/or clinical research coordinator II guidance. + Assists ... and will all relevant local, federal and state regulatory and institutional policies. Responsibilities ESSENTIAL DUTIES- The percentage of time spent performing… more
- Rush University Medical Center (Chicago, IL)
- …coding. Certifications may include Certified Professional Coder (CPC), Certified Coding Specialist (CCS) and Certified Medical Coder (CMC), and any other specialized ... (CPT), ICD-10-CM, and Healthcare Common Procedure Coding System (HCPCS) Level II . * Excellent written and oral communication skills. * Strong investigative… more
- University of Michigan (Dearborn, MI)
- …### or [email protected] , Academic Program Manager, ABA Clinical Faculty Search. Review of applications will begin in early Fall 2024 and will continue until ... (25-40%) + Fulfill the position of Instructor of Record for ABA II Practicum, Behavioral Assessment Practicum, Research Methods in ABA Practicum (includes regular… more
- HonorHealth (Scottsdale, AZ)
- Overview *$5,000.00 Sign-On Bonus! Location: MEDICAL PLAZA II SHEA 10290 N 92nd St SCOTTSDALE, Arizona 85258 United States Work Arrangement: Fully on-site Schedule: ... statistical information on clinical research as required by the Institute, System. IRB , or investigators. Assists with the creation and implementation of tools to… more
- Astellas Pharma (Northbrook, IL)
- …in remote work are encouraged to apply. **Purpose and Scope:** A Clinical Site Manager II (CSM II ) serves as the primary contact point between the Sponsor and ... partner with Clinical Trial Lead (CTL,) Clinical Trial Manager (CTM,) Clinical Trial Specialist (CTS,) and Study Start-Up Specialist (SSS) to ensure overall site… more
- Stanford Health Care (Palo Alto, CA)
- …the supervising physician, enrolls patients in investigational studies approved by the Investigational Review Board ( IRB ), and orders the necessary tests and ... with the attending physician. Other responsibilities include consultation with specialist providers and other team members regarding findings/changes in patient… more
- SpaceX (Hawthorne, CA)
- …long-term vision for the research program + Support in-flight research activities as specialist on console in Mission Control + Work with customers in development of ... to writing or reviewing academic presentations and publications + Apply for IRB approval and develop informed consent + Contribute to medical system design… more
- Stanford Health Care (Palo Alto, CA)
- …the supervising physician, enrolls patients in investigational studies approved by the Investigational Review Board ( IRB ), and orders the necessary tests and ... Advanced Practice Provider (Nurse Practitioner, Physician Assistant or Clinical Nurse Specialist ) on the inpatient neurosurgery service. the service covers 24 hours… more
- Stanford Health Care (Palo Alto, CA)
- …the supervising physician, enrolls patients in investigational studies approved by the Investigational Review Board ( IRB ), and orders the necessary tests and ... with the attending physician. Other responsibilities include consultation with specialist physicians and other team members regarding findings/changes in patient… more