Vacancies : Clinical Research Associate (Covance)

Job Title             :  Clinical Research Associate II

Company Name : Covance

Job Code            : 32867BR 

Locations           : India

Qualifications    : University/college degree (life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
Experience        : Minimum of four(4) years of clinical research monitoring experience (including pre-study, initiation, routine monitoring and closeout visits)
 
Skills and knowledge:

• Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements 
• Thorough knowledge of monitoring procedures
• Basic understanding of the clinical trial process
• Ability to monitor study sites independently according to protocol monitoring guidelines, SOPs, GCP and ICH Guidelines
• Have a full understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
• Good planning, organization and problem solving abilities
• Ability to work with minimal supervision
• Good communication and interpersonal skills
• Good analytical and negotiation skills
• Computer competency
• Fluent in local office language and in English, both written and verbal
• Works efficiently and effectively in a matrix environment

Job Profile : 

• Assures the implementation of project plans as assigned 
• Site administration and site monitoring responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP
• Site management responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP 
• Act in the project role of as Local Project Coordinator or Lead CRA as assigned

To Apply this job Click Here