Clinical Regulatory Affairs Career Research and Resources
Environdyne
Avg. Salary: $226,000 · Company Rank: Not Available
CSR, Inc.
Task leader for the development of the Alcohol and Other Drugs Thesaurus for the National Institute of Alcohol Abuse and Alcoholism. The thesaurus was designed to optimize searches in the Alcohol and Alcohol Problems Science Database.
Avg. Salary: $124,800 · Company Rank: 4.0 out of 5
Progressive Technologies Management, Inc
Work as editor and content analyst on JanssenMD™, which provides free access to scientific and clinical information and services for a number of products marketed by the Janssen Pharmaceutical Companies of Johnson & Johnson.
Avg. Salary: $124,800 · Company Rank: 4.0 out of 5
Amgen Inc.
Orchestrated component/submission publishing for major initiatives. Ensured compliance of clinical study reporting, protocols, statistical analysis plans, and other documentation on investigational and marketed products for electronic publication and distribution. Prepared and submitted hundreds of dossiers to Food and Drug Administration in collaboration with regulatory affairs clients.
Avg. Salary: $67,500 · Company Rank: Not Available
University of Castille-La Mancha
Lectures on "How to Write a Scientific Paper" for postgraduate students in social and health sciences.
Avg. Salary: $124,800 · Company Rank: Not Available
University of Alcala de Henares, Department of Medicine
Development of a 20-hour course for postgraduate students on "How to Write a Scientific Paper"
Avg. Salary: $124,800 · Company Rank: Not Available
Jarpyo Editores (now Aula Medica)
Management of translations into Spanish of books and journals. Worked with teams of translators on multiple simultaneous projects.
Avg. Salary: $124,800 · Company Rank: Not Available
Kalman & Co. Inc
As part of an integrated product team, my role consisted in extensive review of study protocols, informed consents, regulatory documentation for FDA submission, data listings, budgets. Participated in collaborations of formal review reports as requested by the government client. Reviewed and commented on contractors monthly progress reports to assure they were performing required tasks according to the project timeline. Rev...
Avg. Salary: $0 · Company Rank: Not Available
Aeras
I continued my involvement with specimen management and clinical supplies responsibilities and other previous responsibilities. The international travel, visit and qualification of potential clinical trial sites continued in England and Switzerland in collaboration with other team members. I continued writing specimen management manuals and participated in SIV in preparation for study starts.
Avg. Salary: $0 · Company Rank: Not Available
Aeras
This period of time was probably one of the most challenging while employed in Aeras as I began performing dual roles of great responsibility. I received the new responsibility of managing the organization's drug supply without prior training. Management trusted that I could perform the duties due to past excellent performance reviews and my capability to make anything happen. I still managed the clinical trial specimens i...
Avg. Salary: $0 · Company Rank: Not Available
