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Manages regulatory activities for new products in order to get products to market according to company plans. Handles timely submission and follow-up of post-approval labeling and CMC variations. Develops drives...
Strong achievement drive and positive attitude, desire for self-improvement. Evaluate and interpret medical literature, abstract and writing medical information in various formats. Ability to review/understand complex scientific and medical data...
Broiler ve Broiler Damızlık saha çalışmalarında saha teknik hizmetlerinin planlanması, uygulanması, raporlanması ve sunulması. Broiler ve Broiler Damızlık sahada Müşteri ihityaçlarına uygun olarak, numune toplama, laboratuvarlarla iletişim, sonuçların takibi ve...
Gather, clean and organize data from various sources to ensure its accuracy and usability for analysis.,. Continuously maintain master data quality of key data assets (e.g. distributors sales/competitors data) through...
Ownership of country and site budgets. Development, negotiation and completion of Clinical Trial Research Agreements (CTRA). Provide support and oversight to local vendors as applicable. Interacts with EC and Regulatory...
Performs clinical study sitemanagement/monitoringactivities in compliance with Good Clinical Practice and associated documents & regulations,. Collects, reviews, and monitors required regulatory documentation for study start-up, study maintenance and study close-out,....
Drug & Non-Drug Supply Management. Payment and Invoice Management. Document & report checks from Veeva. Preparation of submissions to regulatory authorities. Management of safety documents. Pre and Post Monitoring Visit...
Manages regulatory activities for new products in order to get products to market according to company plans. Handles timely submission and follow-up of post-approval labeling and CMC variations. Develops drives...
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