长沙招聘

We are looking for talented clinical research professionals for Clinical Data Associate 临床数据专员 in Beijing and Shanghai. If you have experience on clinical data management, we would like to talk to you about Clinical Data Associate 临床数据专员 opportunity.

Clinical Data, Analysis, and Reporting Organization (CDARO) is providing our clients with unique, reliable and fully integrated service to help them bring the miracles of medicine to market sooner. With CDARO, you have the opportunity to work with some of the biggest names in the pharmaceutical industry. We offer you with a learning environment, comprehensive insight and the road to career success.

Primarily responsibilities of a Clinical Data Associate:

Review clinical trial data in accordance with Global Data Management Plans and applicable standardized data management processes (SOPs, Work Instructions, etc.) to identify erroneous, missing, incomplete, or implausible data

Run ancillary programs (e.g., diagnostics, special listings, reconciliation discrepancy listings) used to support the review of clinical trial data

Generate, resolve and track queries to address problematic data identified during data review activities and apply proper modification / correction to the database

Apply quality control procedures and checks to ensure data quality standards (client and Covance) are achieved

Assist with the reconciliation of central laboratory and/or third party vendor data

Assist with the aggregate review of clinical data by patient, site and /or project to identify data trends (patient safety, compliance, etc.) and/or data inconsistencies that require further investigation


Education/Qualifications


University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)


Experience


Approximately 18 months experience in related field (e.g. pharmaceutical, laboratory, data analysis) incorporating approximately one year’s clinical data management experience will be considered

Good concentration skills are required to meet the consistently high standards expected

Flexibility – being able to move from one computer system to another with ease, and adapt to new technology and a constantly changing work environment


About Covance:

Covance is one of the world’s largest and most comprehensive drug development services companies, with more than 11,000 employees in 60 countries. We began operations Asia Pacific in 1988 and today have more than 1000 employees in 14 countries across the region. Through our discovery, nonclinical, clinical and commercialization services, Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today.


Why Covance?

At Covance, we help make the miracles of medicine a reality. We offer opportunities to work on diverse, challenging projects with bright, interesting colleagues while building a flexible and rewarding career.

We welcome your application and believe this decision may be the most rewarding career move you will ever make!

Covance is one of the world’s largest and most comprehensive drug development services companies with more than 10,000 employees in 60 countries. Through its nonclinical, clinical and commercialization services, Covance has helped pharmaceutical and biotech companies develop one-third of all prescription medicines in the market today.

Well come to our online job pool to dig out more opportunities at:
http://careers.covance.cn/