CRA临床监察员--沈阳

Are you a Clinical Research Associate who wants to work with one ofleading global CROs in the industry? Covance is seeking CRAs with atleast 1 year clinical monitoring experience NATIONWIDE, an******** avariety of CRA needs in Phase II-IV an******** I (Early ClinicalDevelopment) in multiple therapeutic areas such as oncology, car********diabetes mell******** en******** etc. Whether you’re ready to make amove or just intereste******** learning more, apply TODAY an********’stalk together!

Covance China is committe******** providing a clinical research careerwith purpose in a culture that values achievement. By joining ourClinical Trial Operations Team, you will work in a collaborativeenvironment with the flexibility to pursue different clinical trialsinvolving various compounds - giving you an excellent overview of bestpractices across the industry. Experience the global reach an********recor******** success from one of the few truly global drug developmentcompanies positione******** provide comprehensive clinical support fromFirst-in-Human studies.

Responsibilitie********
Clinical Research Associate performs site management, siteadministration an******** monitoring responsibility for clinical studiesaccording to Covance Standar******** Proce******** ICH Guidelinesan********, including pre-study qualification an******** v********routine mon******** close-out of clinical s******** an******** of studyfiles.
Responsibilities an******** ******** but are not limite******** thefollowing:
• Take charge of all aspects of Site Management as prescribe******** theproject plans.
• Recruit potential ******** prepare EC subm******** notify regulatoryauthor******** translate study-relate********, an******** meetingsan******** tasks as instructe******** supervisor.
• Negotiate study budgets with potential investigators an******** withthe Covance legal department with statements of agreements as assigned.
• Complete Serious Adverse Event (SAE) report******** process productionof reports, narratives an******** up of SAEs.
• Independently perform CRF review; query generation an******** againstestablishe******** review guidelines on Covance or client datamanagement systems as assigne******** management.
• Assist with tra******** mentor******** an******** of new employees,e.g. co-monitoring.
• Perform other duties as assigne******** management.

Education/Qualification********
• University/college degree (life science preferred), or certificationin a relate******** health profession from an appropriatelyaccredite******** (e.g., nursing cert******** medical or laboratorytechnology).

Experience:
In lieu of the above re******** candidates with three or more years ofrelevant clinical research experience in pharmaceutical or CROindustries will be considered.
• Ability to monitor study sites independently according to protocolmonitoring gu******** S.O.P.s, GCP an******** Guidelines.
• Have a full understanding of the Serious Adverse Event (SAE)report******** process production of reports, narratives an******** upof SAEs.
• CRA II positions require 2+ years of clinical research monitoringexperience
• Senior CRA positions require 4+ years of clinical research monitoringexperience. Alternatively candidates with 4+ years supervisoryexperience in a health care setting an********+ years clinical researchexperience in the pharmaceutical or CRO industries (includingmonitoring) may also be considered.

Preferred:
One or more additional years of experience in a relate******** (i.e.me******** cl******** pharmaceut******** laboratory, research, dataanalys******** data management or technical writing) is preferred. Moreyears of experience preferre******** apply senior level CRA positions.

About Covance:
Covance is one of the world’s largest an******** comprehensive drugdevelopment services compan******** with more than 11,000 employees in60 countries. We began operations in Asia Pacific in 1988 an********have more than 1000 employees in 14 countries across the region. Throughour ******** noncl******** clinical an******** serv******** Covance hashelpe******** an******** companies develop one-thir******** allprescription medicines in the market today.

Why Covance China?
At Covance Ch******** you will join like-minde******** who, together,buil******** reputation as one of the world's largest an********respecte******** research organizations. In choosing Covance Ch********you will be part of a dedicate******** that makes a difference inhelping to deliver life-saving an********-enhancing medicines to peoplearoun******** world.

We Offer
Covance’s ongoing success offers team members unsurpasse********an******** development opportunities. At Covance Ch******** we help makethe miracles of medicine a reality. We offer opportunities to work on******** challenging projects with br******** interesting colleagueswhile building a flexible an******** career.

There is no better time an******** to join us!