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Online Resumes with "REGULATORY AFFAIRS"
VP Regulatory Affairs and Quality Assurance
I am currently looking for an ethical company in the medical device or pharmaceutical industry that can utilize my experiences including but not limited to the scope of quality, of which I have been responsible for recruiting and adjusting personnel levels, QA Incoming Inspection (components and raw materials using sampling plans from ASQ Z1.4, MIL 105E and in-house specifications for inspections), QA Finished Product Relea...
Agricultural Technician
Tags for this Online Resume: Regulatory Submissions, Clinical Research Associate, Regulatory Compliance, Regulatory Affairs, clinical research coordinator
Administrative Assistant/Regulatory Affairs specialist
10 years of Pharmaceutical experience in Regulatory affairs and 3 years of Administrative Assistant for VP,CFO's and Directors
Regulatory Affairs Associate
To secure employment in the Regulatory Affairs department where I can utilize my scientific background along with my hands-on experience in writing and compiling common technical documents (CTDs)for the purpose of maintaining and progressing the company’s growth.
Regulatory Affairs Specialist
I Seek a fulltime Regulatory Affairs professional position that will utilize the achievements, skills, strategic thinking and leadership abilities that enable me to aid the company in timely submission packets; Wereby we consistently exceed earnings potentials and achieve company goals in any of today's global economic markets.
Tags for this Online Resume: Regulatory Affairs Professional, FDA 510(k), PMA, IDE, ICH, CE Markings, EU MDD, CMDCAS
Senior Regulatory Writer (17 years experience)
I am seeking to end my present consulting status and return to an in-house position where continuity of projects is more realized. I have over 15 years experience writing regulatory medical documents that comprise CFR21 356h NDA/BLAs and eCTDs deliverables to the FDA/EU/Canadian regulatory authorities. I have written approximately 85 CSRs and can confidently say that ~40 of these were NCEs, early phase I/II and some pha...
Tags for this Online Resume: Regulatory Medical Writer Manager level
Drug Safety /Pharmacovigilance manager
To join, contribute and grow within the dynamic pharmaceutical / biotechnology / CRO environment. The areas of drug safety, pharmacovigilance, medical information, medical scientific liaison, regulatory and medical affaires are in my particular interest.
Tags for this Online Resume: drug safety, pharmacovigilance, medical information, medical affairs, madical scientific liaison, regulatory affairs
Clinical Regulatory Affairs
DIRECTOR/ASSISTANT DIRECTOR
HIGHLY SKILLED IN PLANNING ACTIVITIES, PROGRAM/SERVICE DEVELOPMENT, KNOWLEDGEABLE IN REGULATORY AFFAIRS, GOOD UNDERSTANDING OF MANAGEMENT SYSTEMS AND OPERATIONS ANALYSIS, COMFORTABLE IN DEMANDING ENVIRONMENT.
Team-oriented, highly organized clinical research professional
I am looking for a career in the clnical research industry in Clinical Operations: clinical study coordinator, regulatory affairs, project management, etc.
Ideal Companies: Pharmaceutical, biotech, CRO company working in Clinical Operations.
Tags for this Online Resume: FDA, ICH, GCP, Regulatory, coordinator, IRB
Healthcare Industry Professional, Chicago
I would like to find a position where I can use my strong scientific backgound and my healthcare industry experience either in a pharmacovigilance area or a regulatory affairs type position dealing with submission of various research documents to the FDA.
Tags for this Online Resume: Data Analysis, Adverse Events, Regulatory Affairs, Pharmacovigilance, Clincal Data Analysis, Clinical Research, Scientific documents
Seeking a Career, NOT a job - Open to all industries
Regulatory affairs, corporate compliance, insurance billing, third party reimbursement
Ideal Companies: no preference
Tags for this Online Resume: compliance, regulatory, pharmaceutical, account management, social services, insurance, risk management, manager
