- Otsuka America Pharmaceutical Inc. (Baton Rouge, LA)
- …working in the pharmaceutical and/or healthcare industry. - Knowledge and experience with preparation of global regulatory submissions (IND, CTA, NDA or BLA, ... **Position Summary** Provides critical support in developing global regulatory strategy, planning and execution of global investigational and marketed prescription… more
- Sumitomo Pharma (Baton Rouge, LA)
- …action or develop the appropriate solution + Contribution to the development and preparation of successful regulatory strategies and the ability to contribute to ... for assigned products. This position is responsible for the preparation , coordination and monitoring of routine US and/or global...the development and writing of a regulatory strategy document + Ability to make… more
- Entergy (New Orleans, LA)
- …services, and utility offerings, including related work papers and supporting schedules. + Document and assist in the interpretation of regulatory order filing ... other Regulatory Services teams for the accurate and efficient preparation of regulatory filings, including but not limited to proforma adjustments, cost of… more
- Oracle (Baton Rouge, LA)
- …risks and deficiencies. + Coordinates the preparation of and may prepare document packages for regulatory submissions from all areas of company as well ... supports the organization in complying with, as well as the ongoing preparation , testing and monitoring of conformance to, the requirements of government regulations… more
- Parexel (Baton Rouge, LA)
- …and applicable regulatory guidelines and regulations. + Broad experience in preparation of all types of clinical regulatory documentation. Experience in ... develop, and finalize key clinical documents for submission to regulatory authorities, without the need for any supervision or...prepare any type of medical writing deliverable. + Revise document drafts based on the review comments from team… more
- Parexel (Baton Rouge, LA)
- …to prepare, develop, and finalize clinical documents for submission to regulatory authorities, including but not limited to: briefing documents, investigator ... informed consents, interim and final clinical study reports, common technical document (CTD) clinical overviews and summaries, safety update/aggregate reports, and… more
- Cleco (Pineville, LA)
- …customer service, and operational excellence. + Responsible for assisting in the analysis, preparation and filing of various regulatory reports as required by ... an experienced professional with knowledge of and some experience with regulatory filing principles, practices, concepts, and theories. Provides rate related… more
- WSP USA (New Orleans, LA)
- …guidance for multi-site/phase planning projects, site and impact assessment, the preparation of general plans, specific/master plans, public involvement, and ... regulatory compliance for a variety of client projects relating...staffing services. Unsolicited resumes include any resume or hiring document sent to WSP in the absence of a… more
- Fresenius Medical Center (Hammond, LA)
- …between treatments according to facility policy. + Conduct all tasks necessary for preparation for dialysis treatment and document where appropriate and perform ... all relevant functions necessary for the discontinuation of treatment - document . + Discontinue dialysis treatment according to established procedures and evaluate… more
- Fresenius Medical Center (Shreveport, LA)
- …between treatments according to facility policy. + Conduct all tasks necessary for preparation for dialysis treatment and document where appropriate, and perform ... all relevant functions necessary for the discontinuation of treatment - document . + Discontinue dialysis treatment according to established procedures and evaluate… more