Company
Bayer China
Location
Beijing, China
Job Type
Contract (1 year)
Pay Rate
Competitive Salary
Years of Experience
Experienced(2-5 Years)
Job Reference Code
J1800986
Bayer is a globalized innovation company with core competencies in the fields of health care and agriculture. Bayer develops new molecules for use in innovative products and solutions to improve the health of humans, animals and plants. Its research and development activities are based on a profound understanding of the biochemical processes in living organisms. Through its products, Bayer is contributing to finding solutions to some of the major challenges of our time. The growing and increasingly aging world population requires improved medical care and an adequate supply of food. Bayer is improving people’s quality of life by preventing, alleviating and curing diseases and the company is helping provide a reliable supply of high-quality food, feed and plant-based raw materials.
• Promptly and accurately identify, interpret and extract adverse event and all relevant corresponding case information from a wide variety of source documents;
• Enter the extracted information into the global database for serious and non-serious AE/ADR case reports;
• Identify information such as product technical complaints in the source documents, which must be further processed by the local affiliate, and forward accordingly;
• Create and review comprehensive medical case narratives with no important gaps regarding the reported information received. Confirm with experienced staff as needed.
Requirements:
• Pharmacist, Veterinarian, Biologist, Nurse, HCP Life Science degree, or similar education with medical or scientific focus ideally with previous PV experience.
• Should be willing and able to quickly develop in-depth understanding of database field structure, and processing rules.
• Should have or quickly develop basic knowledge of ICH principles of SAE/AE reporting along with basic understanding of local and global regulatory rules and regulations and basic knowledge of safety policies and procedures in the major countries.
• Should have or quickly develop good understanding of AE and drug coding conventions (MedDRA, WHO-DD).
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