The main tasks will consist of the following:

- Managing the safety of the medicines sold and being researched. Also, establishing proper plans for maintaining the best profit/risk balance and maximizing commercial value.
- Creating and maintaining a system for the compilation, processing and evaluation of the information on all suspicions of adverse reactions reported to the company\'s personnel.
- Preparing and submitting the periodic reports on safety to the Spanish Medicines and Health Products Agency and ensuring that a swift and thorough response is given to any request for information which that agency makes.
- Ensuring regulatory and legal compliance in terms of pharmaceutical surveillance, in terms of medicines sold and researched.
- Analyzing and recording the safety information on medicines and products, RAM (adverse medicine reaction) notifications and publications, as well as those on competition.
- Cooperating with the Clinical Research Department (as of Stage I in humans) to design clinical trial protocols.
- Establishing a pharmaceutical surveillance plan for medicines sold and products which involves the sales network, including an ongoing training plan.

Requirements

- University Degree in Medicine/ Life sciences
- Minimum of 5 years performing similar tasks


SEC Pharma People are acting as an Agency and or Employment Business
For a confidential consultation call Manpreet on 0044 (0) 207 255 6600 or email your CV to
manpreet.mangat@SECpharma.com

SEC Recruitment Limited is acting as an Employment Agency and/or Employment Business