Job Description
• Site administrating and site monitoring responsibility for clinical studies according to Covance Standard Operating Procedures, ICH Guidelines and GCP;
• Recruiting potential investigators, working with start-up department for EC submissions, translating study-related documentation, organizing of meetings and other tasks as instructed by supervisor;
• Completing Serious Adverse Event (SAE) reporting, processing production of reports;
• Negotiating study budgets with potential investigators and assisting the Covance legal department with statements of agreements as assigned.
• Recruiting potential investigators, working with start-up department for EC submissions, translating study-related documentation, organizing of meetings and other tasks as instructed by supervisor;
• Completing Serious Adverse Event (SAE) reporting, processing production of reports;
• Negotiating study budgets with potential investigators and assisting the Covance legal department with statements of agreements as assigned.
Requirements
About You:
• University Degree (life science) or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology);
• Fluency in local and English language.
• Understanding of the clinical trial process;
• Minimum 1 year of monitoring experience in pharmaceutical or CRO industries;
• Thorough knowledge of ICH Guidelines and GCP including a basic understanding of regulatory requirements;
• Thorough knowledge of monitoring procedures.
Company offers
How to apply:
To apply, please visit our website at careers.covance.com and look for the reference 44909BR.
You can also follow the link: http://careers.covance.com/job-postings/44909BR/clinical-research-associates-1-or-2-or-senior
EEO Employer: Covance is committed to diversity in the workplace and is an equal opportunity employer (Minority/Female/Individual with Disability/Veteran). Your confidentiality and privacy are important to us.
