- Locations: California, Florida, New Jersey, Ohio, Texas
- Related Keywords: Clinical, Clinical Document, Clinical Document Control Assistant, Control, Document, Document Control
- Regulatory Affairs Project Manager-Pharma
- Manpower (Lake Bluff, IL)
- ...setting preferred. Familiarity with FDA, GMP, compliance standards and document control processes and software necessary.Position is a... clinical knowledge in pharmaceutical industry, regulatory affairs, document control , FDA, GMP. Manage and coordinate several...
- Technologist, Medical I
- Quest Diagnostics (Kansas City, KS)
- ...in their respective guidelines. ยท Adhere to the laboratory's quality control policies, document all quality control activities,...must provide a detailed original transcript. Work Experience: 1 year Clinical experience (high complexity testing) preferred. Minimum of 1 year of...
- Sr Prin Compliance/Audit Spec
- Medtronic (Minneapolis, MN)
- ...Manufacturing support services as well as other functional/process areas to be determined such as Product Development, Supply Chain, Regulatory, Clinical , or Document Control . Future client focus may change based on business needs. . Support Q*STAR Phase II improvement projects...
- Sr. Document Control Associate (pharma, medical device)
- Shore Consultants (Nashville, TN)
- ...products and a robust pipeline of R&D, preclinical and clinical product candidates. Growth orientated, zero employee turnover, no hidden...Quality clients. Quality candidates. Quality process. Summary: The Senior Document Control Associate is responsible for all the...
- Document Control Specialist
- Thermage, Inc. (Hayward, CA)
- Document Control Specialist Job Type: Full-Time Location: Hayward, CA Last Updated: 03/24/2009 Job Description:...As the leader in fractional laser technology, Fraxel delivers minimally invasive clinical solutions to resurface aging and sun damaged skin. Since 2002, approximately...
- Supervisor Document Control (EDMS)
- Dendreon Corporation (Seattle, WA)
- Supervisor Document Control (EDMS) Job Type: Regular Full-Time Location: Seattle, WA Job Description: Dendreon...records are controlled and archived by the quality organization for GMP clinical and commercial usage including procedures, test methods, master batch records,...
- Document Control Coordinator
- Stryker (Portage, MI)
- Job Title Document Control Coordinator Division Stryker Instruments Location (Country - State) United States - Michigan City or Sales Region Portage Business Function Regulatory/Quality/ Clinical Affairs Shift 1st Education and/or Special Training High school diploma required....
- Document Control Specialist
- Unknown (San Antonio, TX)
- ...candidate to assist the Human Resources Department of a local clinical research organization in Austin, TX. Qualified candidates will have...conducting initial phone screens. Prior experience with scientific, healthcare or clinical staffing is a plus, but not required. Salary is...
- Document Control Specialist
- Unknown (Madison, NJ)
- ...base information on our products, ingredients and general information regarding registration information. Overall responsibilities include: * Publishing of Clinical Study Reports and Electronic submissions * Perform data entry for compliance and product information databases * Provide...
- Document Control /Quality Assurance/Regulatory/Label Specialist
- Ultimate Staffing Services (Irvine, CA)
- ...Identifies labeling issues, including those raised by team members outside of R&D, such as worldwide operations, marketing, regulatory affairs and clinical affairs. Works with the initiator and/or project leader, team leader and the team to define and implement solutions. Structures...
- Medical Writing/ Document Specialist or Sr. Medical
- Bayer (Montville, NJ)
- ...Document Specialist is responsible for the compiling, tracking, quality control and timely completion of the document components...Process Management and Medical Writing and the Vive President of Clinical Pharmacology. The Medical Writing/ Document Specialist, reporting...
- QA GCP Auditor
- Unknown (PA)
- ...of departmental SOPs.Utilize spreadsheets to track, trend and generate required reports.Alert Director QA-GCP of internal and external GCP, document control , compliance and clinical trial issues in a timely manner.Be thoroughly familiar with compounds, protocols, case report...
- Manager, Regulatory Affairs
- BioTech Company (Boston, MA)
- ...primarily supporting complaints & adverse events and submission of clinical trial applications to regulatory agencies. This position acts as...Affairs to ensure regulatory reporting requirements are assessed and document . Prepare and submit medical device and adverse event reports...
- Medical Case Manager
- Travelers (Buffalo, NY)
- ...specialty resources to achieve appropriate claim outcomes (SIU, Legal, Risk Control , Disability Management, IME and Peer Review vendors, Major Case,...for assignment to Medical or Vocational Case Manager, or vendor. Document all contacts and outcomes related to case activity in...