天津招聘

Responsibilities/Duties
? Support the delivery of the Clinical and Ancillary supplies component of assigned studies within the region.
? Act as contact with study team during clinical and ancillary start-up activities including input to the development of Clinical Trial Supplies Plan
? Perform and coordinate label review and country translations according to set procedures for a global study.
? Responsible for working with project team to ensure the required documents and processes related to supply management are communicated and obtained.
? Where appropriate be the key contact for importation logistics and document exchange to ensure smooth clinical supply transportation arrangements are agreed and set up.
? Provide consultancy with regard to clinical & ancillary supply distribution strategy for the assigned country(ies) in the region.
? Responsible for maintenance of project specific clinical & ancillary supply logistics.
? Work closely with drug and ancillary supply distribution, IVRS/IRT and label translation vendors during the set up and maintenance of related logistics
*Education/Qualifications
University/College degree (life science preferred), or certification in a related allied health profession from an appropriate accredited institution (e.g., nursing certification, medical or laboratory technology)
*Experience
?Minimum of 2 years relevant clinical research experience in a pharmaceutical company/CRO, including at least 1 year of experience in Clinical Supply distribution/ GMP environment
? Working knowledge of ICH, FDA, GMP and other applicable regulations/guidelines; familiarity with clinical supply related documents
? Strong networking abilities and an ability/willingness to work with internal and external stakeholders across the globe
? Good organizational and time management skills
? Excellent communication / writing skills
? Strong computer skills with an ability to access and leverage technology alternatives
? Abilities to review/analyze relevant data so as to assist in building evidence-based clinical trial strategies
? Self-motivation with the ability to work under pressure to meet deadlines
? Works well independently as well as in a team environment
? Detail and process oriented
? Positive attitude and approach
? Multi-tasking capability
? Ability to work independently

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/