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Training Pathway: Clinical Data Management:
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 development process and roles/opportunities in Clinical Research. Ethical issues in clinical research and their impact on the development of new products. Institute and obtain proper Informed Consent. Understanding the recent Good Clinical Practices (GCP) and 21 CFR Part 11 regulations. Understanding of FDA and ICH Regulations for Clinical Research industry. Identification of adverse effects and proper reporting format. Develop qualifications sought by the Pharmaceutical, Biotech & Medical Device industry. Many real world and practical points in successful trials.
Understanding of clinical data management as per FDA and ICH, GCP, 21 CFR Part 11 regulations. GCDMP, CRF designing and annotations, Oracle Clinical DB concepts, introduction to CDISC, medDRA coding, computer system validation. Inroduction to SQL. Overview of Oracle Clinical and other clinical data management applications. Understanding and review of clinical protocol, SOPs, overview of study setup, data entry and data analysis.
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Duration:: 4-6 weeks |
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Required Education:: Bachelors/Masters in Healthcare, Medicine, Nursing, Pharmacy,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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