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Online Resumes with " Regulatory Affairs"
Manager
I bring over twenty-four years of security and technology experience, most recently as a Director in Information Risk Management. In this role, I am leading the strategy, deployment and execution of critical security programs for a Fortune 21 Company. I have opportunities to collaborate closely with other Corporate disciplines including Legal, Privacy, Compliance, Regulatory Affairs and Technology in the identification an...
FM
A senior level regulatory medical writing position in a pharmaceutical company.
Tags for this Online Resume: Regulatory affairs, Medical writer, molecular biology, biochemistry, clinical development, drug
Clinical Regulatory Affairs
Tags for this Online Resume: Report Writer (Toxicology), Quality Assurance, Preclinical Regulatory Affairs
Clinical Regulatory Affairs
Manager of Regulatory Affairs
Regulatory Affairs Professional
Sr. Clinical research Associate/ Director of clinical research
Can undertake most of the tasks and works independently. Very much focussed on the timelines and quite goal tending. Willing to help others in their prioritized tasks. Excellent planning, design and implementation. Highly experienced in writing reports and data analyses.
Ideal Companies: Pharmaceutical industries, Biotech companies, Research institutes, hospitals and for profit mid to large companies.
Tags for this Online Resume: Director of clinical research, Manager of drug safety, Senior clinical research associate, Regional clinical research associate
Multiple Area's of Expertise Available
Excellent multi-task ability and skilled in MS Word, Excel, PowerPoint and multiple database applications.
Regulatory Affairs Specilist
REGULATORY AFFAIRS INTERNSHIP
GAIN MORE KNOWLEDGE AND UNDERSTANDING OVER REGULATORY AFFAIRS INTERNATIONALLY
Regulatory Affairs Assistant, Durham/RTP
Seeking a full-time position utilizing my written,organization skills in a government, health care, clinical research setting with an emphasis on regulatory affairs submissions, informed consent, and FDA requirements
