| Resume alert | Resumes 11 - 20 of 574 |
Analytical, great communicator, strategic, planning & organized
Pennsauken, NJ
... lung, and gastric cancers across 15 sites in the United States from start-up activities including feasibility, final protocol, FDA follow-up, study and site contracts and budgets, master ICF development and approval, oversight of site ICF ... - Feb 18
... lung, and gastric cancers across 15 sites in the United States from start-up activities including feasibility, final protocol, FDA follow-up, study and site contracts and budgets, master ICF development and approval, oversight of site ICF ... - Feb 18
Database Administrator Sql Server
Princeton, NJ
... Created multiple Oracle instances for Argus Safety & Risk management application according FDA regulations. Setup and Configure HA solution using Oracle physical standby database. Recover standby database as and when required. Monitor and ... - Feb 14
... Created multiple Oracle instances for Argus Safety & Risk management application according FDA regulations. Setup and Configure HA solution using Oracle physical standby database. Recover standby database as and when required. Monitor and ... - Feb 14
Supply Chain General Manager
Somerset, NJ
... P&L Management - *Technical:* Project Management, Hazmat Certified, 5S & LEAN, Microsoft Suite - *Regulatory:* DOT, FDA, OSHA, Safety & Security Control **Professional Experience:** **United Parcel Services (UPS) - Transportation Department* ... - Jan 23
... P&L Management - *Technical:* Project Management, Hazmat Certified, 5S & LEAN, Microsoft Suite - *Regulatory:* DOT, FDA, OSHA, Safety & Security Control **Professional Experience:** **United Parcel Services (UPS) - Transportation Department* ... - Jan 23
Consultant in CNS drug development, substance use disorder treatments.
New Brunswick, NJ, 08989
... external studies supporting risk mitigation strategies Led global efforts in automation of data capture and Robust Study Design for In Vivo Studies Provided post-marketing support to FDA queries on older small molecules as well as the HIV portfolio. ... - Jan 22
... external studies supporting risk mitigation strategies Led global efforts in automation of data capture and Robust Study Design for In Vivo Studies Provided post-marketing support to FDA queries on older small molecules as well as the HIV portfolio. ... - Jan 22
Medical Affairs and Medical Information Post-Doctoral Fellow
Princeton, NJ
... (KOL) as aligned with medical strategy ● Experienced in promotional review committees to ensure medically supported data through commenting, improving, approving, or rejecting material based on established company practice and FDA regulation. ... - Jan 22
... (KOL) as aligned with medical strategy ● Experienced in promotional review committees to ensure medically supported data through commenting, improving, approving, or rejecting material based on established company practice and FDA regulation. ... - Jan 22
Customer Service Management Experience
Horsham, PA
... In compliance with SOPs and Food & Drug Administration (FDA) guidelines, performs venipuncture on donors to begin pheresis process. Make necessary adjustments in order to expedite donation time and ensure product quality and donor safety. Maintains ... - Jan 19
... In compliance with SOPs and Food & Drug Administration (FDA) guidelines, performs venipuncture on donors to begin pheresis process. Make necessary adjustments in order to expedite donation time and ensure product quality and donor safety. Maintains ... - Jan 19
Customer Service Quality Assurance
Plainsboro Center, NJ, 08536
... skills Courteous demeanor Adaptive team player Energetic work attitude Opening/closing procedures Staff Development FDA Compliance Problem-Solving Skills Regulatory Compliance Quality Assurance and Control Patient Education and Counseling ... - Jan 17
... skills Courteous demeanor Adaptive team player Energetic work attitude Opening/closing procedures Staff Development FDA Compliance Problem-Solving Skills Regulatory Compliance Quality Assurance and Control Patient Education and Counseling ... - Jan 17
Clinical Research Business Development
Trenton, NJ
... specified market share in selected therapeutic areas with great emphasis in being competitive in drug labeling and promotion activities within FDA guidelines and industry standard with investigative activities to ensure compliance in all functions. ... - Jan 15
... specified market share in selected therapeutic areas with great emphasis in being competitive in drug labeling and promotion activities within FDA guidelines and industry standard with investigative activities to ensure compliance in all functions. ... - Jan 15
Software Development Health Care
East Windsor, NJ
... Strong knowledge about Pharmaceutical/Medical device regulations like FDA: 21 CFR Part 210, 21 CFR Part 211 and 21 CFR Part 820 and involved in implementation of CFR Part 11 rules (Electronic Records, Electronic Signatures, Audit Trails, and ... - Jan 06
... Strong knowledge about Pharmaceutical/Medical device regulations like FDA: 21 CFR Part 210, 21 CFR Part 211 and 21 CFR Part 820 and involved in implementation of CFR Part 11 rules (Electronic Records, Electronic Signatures, Audit Trails, and ... - Jan 06
Inventory Specialist Medical Device
Somerset, NJ, 08873
... Possessed in-depth knowledge of FDA, DEA, cGMP, GLP, OSHA, EHS, SOP, Parts 210 & 211, and Federal regulations. Professional Experience Ethicon - Med-Tech, Raritan, NJ 08/2022 – Present Sample Management – Global Product Stability, R & D - Biosurgery ... - Jan 04
... Possessed in-depth knowledge of FDA, DEA, cGMP, GLP, OSHA, EHS, SOP, Parts 210 & 211, and Federal regulations. Professional Experience Ethicon - Med-Tech, Raritan, NJ 08/2022 – Present Sample Management – Global Product Stability, R & D - Biosurgery ... - Jan 04