长沙招聘

Serve as Associate Project Manager reporting into PM/SPM/PD for domestic and/or international (typically intercontinental) projects for one or more clients, according to Covance Standard Operating Procedures, ICH Guidelines and GCP
Responsible for the successful conduct of assigned projects.
Serve as Associate Project Manager for assigned business development opportunities.
Liaise with senior management in the Project Management and Clinical Operations as well other Service Delivery Centers to ensure adequate resources are available for assigned projects.
Responsible for assisting the PM/SPM/PD to achieve on time, on-budget provision of client deliverables for assigned projects.

Position can be based either in Shanghai or Beijing.
Required:
University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution, nursing certification, medical or laboratory technology.
In lieu of the above requirement, candidates with five (5) or more years of relevant clinical research experience in pharmaceutical, CRO industries or experience in a health care setting will be considered.
Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements in other countries.
Thorough understanding of the drug development process.
Fluent in local office language and in English, both written and verbal.
Preferred:
Thorough knowledge of Covance SOPs regarding site monitoring.
Experience as a Senior Clinical Research Associate, whether internal or external
Experienced/Skills
Minimum of four (4) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits).
In lieu of the above requirements, candidates with > six (6) years supervisory experience in a health care setting and four (4) years clinical research experience in the pharmaceutical or CRO industries (including monitoring) will be considered.
In lieu of the above requirements, candidates with five (5) years of site management and/or study co-ordinator experience will be considered.
Have a full understanding of Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.
Excellent site monitoring skills.
Excellent study site management skills.
Ability to work with minimal supervision.
Good planning and organization skills.
Good computer skills with good working knowledge of a range of computer packages.
Excellent verbal and written communication skills.
Ability to train and supervise junior staff.
Ability to understand and work with financial information as well as experience predicting or estimating hours and resource levels
Ability to resolve project-related problems and prioritizes workload for self and team.
Ability to work within a project team.
Works efficiently and effectively in a matrix environment.
Preferred:
One (1) or more year's additional experience in a related field (i.e. medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred.
Local project coordination and/or project management.

You can refer and submit CV by system or email to calvin.xu@covance.com

You are strongly encouraged to visit our recruitment website as http://careers.covance.cn/

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/