| Resume alert | Resumes 1 - 10 of 584 |
Information Technology Project Management
Natick, MA
... Electronic CTD submissions to the FDA. Electronic Lab Notebook. • International project manager for Cisco VOIP deployment. • Vendor management for enterprise applications, infrastructure, data and voice. SLA contractual agreements and negotiations. ... - Apr 23
... Electronic CTD submissions to the FDA. Electronic Lab Notebook. • International project manager for Cisco VOIP deployment. • Vendor management for enterprise applications, infrastructure, data and voice. SLA contractual agreements and negotiations. ... - Apr 23
Quality Assurance Clinical Trials
Boston, MA
... Extensive knowledge of pharmacy operations, FDA regulatory affairs, clinical trials of GCP, GMP & GLP, and quality assurance. Proven track record of proper customer advisement and an empathetic attitude towards customers. Superior training and ... - Apr 22
... Extensive knowledge of pharmacy operations, FDA regulatory affairs, clinical trials of GCP, GMP & GLP, and quality assurance. Proven track record of proper customer advisement and an empathetic attitude towards customers. Superior training and ... - Apr 22
Clinical Research Regulatory Affairs
Brookline, MA
... Regulatory Affairs GPA: 4.0/4.0 Relevant Courses: Regulatory Compliance, FDA Pharmaceutical Regulation, Regulatory Strategy for Product development and lifecycle management, Safety sciences, Human experimentation: methodological issues fundamentals. ... - Apr 20
... Regulatory Affairs GPA: 4.0/4.0 Relevant Courses: Regulatory Compliance, FDA Pharmaceutical Regulation, Regulatory Strategy for Product development and lifecycle management, Safety sciences, Human experimentation: methodological issues fundamentals. ... - Apr 20
Digital Innovation - Strategic Partnerships
Cambridge, MA
... Draft Business plan with M&A opportunities, FDA/CMS regulations, and ISV market analysis. Revenue N/A CommonWealth Care enterprise Medicare, Medicaid Cloud platform. Gather requirements and manage ISV partners for Enrollment, Reconciliation and ... - Apr 08
... Draft Business plan with M&A opportunities, FDA/CMS regulations, and ISV market analysis. Revenue N/A CommonWealth Care enterprise Medicare, Medicaid Cloud platform. Gather requirements and manage ISV partners for Enrollment, Reconciliation and ... - Apr 08
Territory Sales Account Manager
Milford, MA
... - 5/07 • Successfully launched new technology in 6 hospitals and 2 physician’s offices within 6 months • Promoted the first FDA approved human implantable microchip to identify chronic illnesses such as, Diabetes, COPD and Alzheimer's HILL-ROM INC, ... - Apr 04
... - 5/07 • Successfully launched new technology in 6 hospitals and 2 physician’s offices within 6 months • Promoted the first FDA approved human implantable microchip to identify chronic illnesses such as, Diabetes, COPD and Alzheimer's HILL-ROM INC, ... - Apr 04
Administrative Assistant Executive
Billerica, MA
... Researched FDA websites, printed documents, emailed to requesting individuals. Contact person for department; interfaced with parent company representatives. Contacted German headquarters for inquiries, sent FedEx packages, scheduled meetings. ... - Mar 28
... Researched FDA websites, printed documents, emailed to requesting individuals. Contact person for department; interfaced with parent company representatives. Contacted German headquarters for inquiries, sent FedEx packages, scheduled meetings. ... - Mar 28
Regulatory Compliance Quality Assurance
Boston, MA
... Conducted a thorough review and presented research on studies conducted for Sotorasib by referencing multidisciplinary review from Drugs@FDA Drafting IND and NDA documents as per eCTD format in compliance with 21 CFR 312. Mumbai University Jan 2021 ... - Mar 27
... Conducted a thorough review and presented research on studies conducted for Sotorasib by referencing multidisciplinary review from Drugs@FDA Drafting IND and NDA documents as per eCTD format in compliance with 21 CFR 312. Mumbai University Jan 2021 ... - Mar 27
Clinical Research Regulatory Affairs
Boston, MA
... Proven track record in improving therapeutic outcomes and streamlining drug therapy processes, demonstrating a solid grasp of GCP, GLP and FDA regulations. EDUCATION: Master of Science in Regulatory Affairs Expected Graduation - December 2024 ... - Mar 22
... Proven track record in improving therapeutic outcomes and streamlining drug therapy processes, demonstrating a solid grasp of GCP, GLP and FDA regulations. EDUCATION: Master of Science in Regulatory Affairs Expected Graduation - December 2024 ... - Mar 22
Project Manager Marketing Communications
Salem, MA
... Babson Development Office (US top Executive diplomacy) Straumann US (dental medical device sales materials generation and research support involving FDA compliance); communications instruction posting in Japan, and Trinity Biotech, Inc., ... - Mar 12
... Babson Development Office (US top Executive diplomacy) Straumann US (dental medical device sales materials generation and research support involving FDA compliance); communications instruction posting in Japan, and Trinity Biotech, Inc., ... - Mar 12
Project Manager Management
Dunstable, MA, 01827
... Most of my projects have entailed standards compliant documentation in preparation for 510k submissions to the FDA. Altran IPD (Formerly Foliage Systems), Burlington, MA 2014 to 2020 Innovative Product Development and technology R&D consulting ... - Mar 08
... Most of my projects have entailed standards compliant documentation in preparation for 510k submissions to the FDA. Altran IPD (Formerly Foliage Systems), Burlington, MA 2014 to 2020 Innovative Product Development and technology R&D consulting ... - Mar 08