- Daiichi Sankyo, Inc. (Bernards, NJ)
- …AE and drug coding conventions (MedDRA, WHO-DD). preferredExtensive knowledge of FDA regulations , clinical and safety databases, preferredFamiliarity with Good ... specific training materials. Manages and coaches the PV Vendor Training Coordinator . Qualifications: Successful candidates will be able to meet the qualifications… more
- SF Staffing Solutions (San Juan Capistrano, CA)
- …to ensure that they are well established and compliant with the regulations . *Establish purchasing controls and work very closely with suppliers of critical ... projects. *Responsible for performing assigned tasks in accordance with applicable safety regulations and instructions, as well as correcting unsafe work habits and… more
- Johns Hopkins University (Baltimore, MD)
- We are seeking a Sr. Credentialing Coordinator oversees the credentialing process for the Johns Hopkins Hospital and Johns Hopkins University for all clinical ... accordance with JHH and JHU School of Medicine policies, government regulations and Joint Commission guidelines. Instruct and advise divisional representatives… more
- Cedars Sinai (Beverly Hills, CA)
- Job Description Come join our team! The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for ... all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board (IRB). Primary duties and responsibilities:… more
- Alcanza Clinical Research (Woodstock, GA)
- …ensure the execution of assigned studies in compliance with GCP, ICH, HIPAA, FDA Regulations and SOPs. Key Responsibilities Essential Job Duties: In ... Clinical Research Coordinator Department: Operations Employment Type: Full Time Location:...protocol, company processes & procedures, and in compliance with FDA , GCP, ICH regulations and guidelines: Screening… more
- UCLA Health (Los Angeles, CA)
- …organizing necessary tasks to ensure adherence to the study protocol and applicable regulations , such as institutional policy and procedures, FDA Code of Federal ... Description The Department of Surgery is seeking a full time Clinical Research Coordinator to contribute to the overall operational management of clinical research /… more
- KDC One Knowlton (New Albany, OH)
- …quality system, FDA Good Manufacturing Practices, OSHA, DOT and EPA regulations , includes maintaining clean and orderly areas at all times. Performs other duties ... nearly 4,800 talented and dedicated employees in North America. Material Control Coordinator - 3rd Shift (M-F; 10:30pm-7:00am) About us: Columbus: Kdc/one is… more
- PLZ Aeroscience (Indianapolis, IN)
- …systems, documentation, audits & training in GMP environment adhering to the ISO and FDA GMP regulations and follows SOPs, GMP, GLP and GDP. Additional ... Wear personal protective equipment Follow company safety policies, rules and regulations Participate in practice evacuation drills-know where the nearest exit is… more
- Claremont Foods (Denver, CO)
- Description JOB TITLE: Bilingual Front Office Coordinator SCHEDULE: FULLTIME/HOURLY NON-EXEMPT Schedule: Monday - Friday (Fully on Site) LOCATION: WESTMINSTER, CO ... and highly organized, dependable and fast learner Bilingual Front Office Coordinator to join our fast-growing team. We offer Health/Dental/Vision Insurance. Paid… more
- McFarland Clinic (Ames, IA)
- McFarland Clinic is currently accepting applications for Clinical Research Nurse/ Coordinator for its Ames office. Candidates should be service-oriented, a team ... of the patient and caregiver regarding the study. Complies with regulations , institutional policies and sponsor requirements governing source data and documentation.… more
- Loyola University Chicago (Chicago, IL)
- Position Details Position Details Job Title CLINICAL RESEARCH COORDINATOR II Position Number 8150021 Job Category University Staff Job Type Full-Time FLSA Status ... grant funded? Yes Duties and Responsibilities The Clinical Research Coordinator II is responsible for the overall management and...submission in compliance with all local, state and federal regulations ; advise the IRB of amendment changes to the… more
- The University of Chicago (Chicago, IL)
- …blood disorders, and experimental therapies. Job Summary The Senior Clinical Research Coordinator (Sr. CRC) is a specialized researcher partnering with the clinical ... of the studies to ensure compliance with federal and institutional regulations . Responsibilities Leads within the department/unit through improving clinical research… more
- Air Liquide (Bay City, TX)
- …in all plant operations including processes/equipment Exhibits understanding of governmental regulations including Food Safety, FDA , Current Good Manufacturing ... systems, and general skill set of technicians. Follows all Food Safety, FDA , and cGMP policies in operating practices. Actively pursuing own growth/career… more
- Cedars Sinai (Los Angeles, CA)
- …study budget and patient research billing. Ensures compliance with all federal, local, FDA , IRB, and HIPAA guidelines and regulations pertaining to the study ... Clinical Research Associate I works directly with a Clinical Research Coordinator , Research Program Administrator, or Research Nurse to coordinate and/or implement… more
- Revival Research Institute, LLC (Evans, GA)
- …of physicians, nurses, technicians, secretarial staff and ancillary hospital staff. Knowledge of FDA Regulations and Good Clinical Practices. JOIN US & GROW YOUR ... Revival now has a national presence in the Metro-Detroit Region, Texas, Illinois, and Georgia. We have been nationally acknowledged for our diligence to provide the highest quality of data for our clinical research trials. As Revival Research Institute is… more
- Cedars Sinai (West Hollywood, CA)
- …Research Associate I works under the direction of a Clinical Research Coordinator , Research Program Administrator, Research Nurse, or other supervising staff to ... all federal and local agencies including the Food and Drug Administration ( FDA ) and local Institutional Review Board. Maintains research practices using Good… more
- Takeda Pharmaceutical Company Limited (Webster, TX)
- …for medical issues. The Medical Support Specialist will be familiar with regulations of the plasma collection industry or a manufacturing environment. The Medical ... to EHS guidance regarding employee incidents. You can be a Pandemic Coordinator when authorized by EHS and support investigations associated with pandemic threats… more
- Cedars Sinai (Los Angeles, CA)
- …samples, kits, and study supplies. This incumbent will follow all federal, local, FDA , IRB, and HIPAA guidelines and regulations pertaining to the study ... provides clerical support to Clinical Research Associate, Clinical Research Coordinator , Research Program Administrator, Research Nurse, or Research Manager. This… more
- Flourish Research (Winter Park, FL)
- …with working in a patient database, such as a CTMS Understanding of ICH, FDA , and GCP regulations Impeccable organizational skills and attention to detail ... Identify and report missing data points or inconsistencies to the clinical research coordinator , QC Manager, Team Leads, and upper management as soon as possible.… more
- Prismatik (Irvine, CA)
- …: Prepare and submit product registrations and submissions (510(k), PMA) to FDA and other regulatory bodies. Maintains company registrations and device listings in ... of conformity in support of EU product registrations/CE mark. Informs coordinator of product recalls. Performs and supports internal, external, and third-party… more
