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Training Pathway: Drug Safety and Pharmacovigilance:
Clinical Research and scientific staffing solutions designed for the Drug Development industry - your Career. Delivered.
Biogensys, has successfully combined the knowledge and expertise with an exclusive focus on the clinical research services and scientific staffing needs of the global Pharmaceutical, Biopharmaceutical and Medical Device industries. Biogensys is one of its kind of companies that can identify and provide right advise for Life Sciences professionals. Explore your career opportunity and how our knowledge and experience driven services and training program can benefit and change your career for a new world.
Worldwide opportunities in the Clinical Research Industry:
At Biogensys, the dedicated management team is from the Scientific and Life Sciences industry with over 20 years of combined industry experience with successful track record in providing clinical research services. Our success is driven by our close interaction with our customers to understand their current and long-term strategic goals and requirements and to provide the best solutions. The process of continuous learning and updating is never stopped at Biogensys, and we keep updated with the recent developments and keep pace with the ever changing industry needs.
Careers in Clinical Research & Drug Development: We are constantly looking for Clinical Research and Life Sciences professionals.
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What you learn:: Drug Safety: Principles of drug safety evaluation, classification of adverse reactions, hypothesis generation and testing, the advantages and disadvantages and principles of spontaneous reporting, methods used to evaluate signals, Pharmacoepidemiological principles and methods, patient and case control studies and the principles of record-linkage. Medical dictionaries and searching strategies. Technolgoy applications that are used in Drug Safety and Pharmacovigilance.
Pharmacovigilance: Monitoring drug safety in clinical Research, identification and responding to drug safety hazards, actions to improve drug safety, postmarketing, monitoring and decision making, lessons learned from previous problems, the pharmaceutical physician and drug safety.
Regulatory requirements for pharmacovigilance: USA – FDA, UK, Europe and International Harmonisation (ICH) in relation to drug safety and Pharmacovigilance. Global assessment of drug safety including risk benefit.
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Duration:: 4-6 weeks |
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Required Education:: Bachelors/Masters in Medicine, Pharmacy, Healthcare, Nursing, any Life Sciences degree. Good understanding of Medical terminology. |
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Technology Tools: Microsoft Office |
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Communication Skills: Good Comm Skills and Written Skills |
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| For further details, please contact us or to send your resume click here. |
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To make a direct contribution and impact with a broad visibility |
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A commitment to learning and development |
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Confidence through prior experience |
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Ability to think independently and perform within a team |
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A balanced and mature business approach |
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The highest degree of ethics and integrity |
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Short and long-term rewards |
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We believe that each employee can make a difference, and we are confident that the rich diversity of perspectives and experiences represented in each of our employees will help us rapidly grow.
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