...conduct RAC assignments by visiting the assigned consignee or by telephone calls, as described in the RAC assignment memo provided by FDA.
Conduct a RAC primarily to confirm the consignee received and followed the instructions in the recall notification and that the...
Suggested
For contractors
...signatures and approvals as directed.
Prepare, submit, and maintain regulatory documents (e.g., IRB, Food and Drug Administration (FDA, etc.).
Process addendums to active protocols.
Document that the IRB has been notified of a protocol change as appropriate....
Suggested
Full time
Shift work
...and administration of study medication Prepares, submits and maintains regulatory documents (e.g. IRB, Food and Drug Administration (FDA), etc.) Processes addendums to active protocols Documents that the IRB has been notified of a protocol change as appropriate Identifies...
Suggested
Full time
Shift work
...of work tasks require prolonged glove wear
**PREFERRED QUALIFICATIONS:**
+ Experience working with SOPs, GDP, GMP, CLIA, and the FDA
+ Experience working in a highly regulated environment
**We Offer Comprehensive Benefits from Day One**
+ Major medical, dental,...
Suggested
Minimum wage
Holiday work
Full time
Temporary work
Traineeship
Local area
Remote job
Relocation
Shift work
Weekend work
Afternoon shift
...complexity testing. • Effectively participate in special projects, quality improvement tasks and projects, workgroups and committees, and CAP/FDA inspection preparation. • Maintain a clean and safe work area, adequate inventory and supply levels, and observe all biosafety and...
Suggested
Traineeship
Immediate start
Shift work
...maximize return within regulatory and ethical guidelines.
* Maintains accountability for all pharmaceutical samples in accordance with FDA and PDMA guidelines.
* Utilize the sales automation system to document call and program activity.
* Complete initial and ongoing...
Suggested
...support for Ruminant products and programs, including response to product inquiries and adverse reports in accordance with internal, FDA, CFIA and USDA regulatory policies.- The position will require developing trial protocols, monitoring and summarizing clinical and marketing...
Suggested
Remote job
Relocation
Visa sponsorship
Flexible hours
Shift work
3 days per week
...requests and problems.
* Sterilizes and discards infectious and disposable waste materials according to Food and Drug Administration (FDA) and Environmental Protection Agency (EPA) regulations.
* Cleans and sterilizes laboratory glassware and equipment and work area....
Suggested
Full time
Temporary work
Part time
...scientific education and dialogue
Excellent stakeholder management, communication, and networking skills
A thorough comprehension of FDA, OIG, HIPAA, and other ethical guidelines, laws, and regulations relevant to the pharmaceutical industry and its customers
Ability...
Suggested
Remote job
Holiday work
Relocation
Visa sponsorship
Flexible hours
Shift work
3 days per week
...activities accurately and in a timely manner;
Responsible for the safekeeping of all medication stock and the records required by the DEA, FDA, and ADP;
Dedicates a minimum of 90% of regularly scheduled work hours to activities directly related to the administration of...
Suggested
Relief
Local area
Shift work
Day shift
Saturday
Early shift
Monday to Friday
...maximize return within regulatory and ethical guidelines.
* Maintains accountability for all pharmaceutical samples in accordance with FDA and PDMA guidelines.
* Utilize the sales automation system to document call and program activity.
* Complete initial and ongoing...
Suggested
Contract work