Clinical Research Assistant and Clinical Project Administrator at Covance

Job description

Main Job Responsibilities

• Provide clinical support for projects according to Standard Operating Procedures, ICH Guidelines and GCP
• Act as contact for project team and study sites
• Assist with the management of study supplies and organize shipments
• Create, update, track, and maintain study-specific trial management files, tools, and systems
• Ensure compliance with SOPs, FDA, ICH, and GCP regulations for clinical conduct in all aspects of daily work
• Assist in submissions and notifications to Ethics Committees and Regulatory Authorities.

Candidate Requirements

• Previous Experience in Clinical Trials is a MUST!
• Degree educated.
• Fluency in English language.
• Understanding of the clinical trial process;
• Good oral and written communication skills
• Ability to set priorities and handle multiple tasks simultaneously

At Covance, you will join like-minded professionals who, together, build our reputation as one of the world's largest and most respected contract research organizations. In choosing Covance, you will be part of a dedicated team that makes a difference in helping to deliver life-saving and life-enhancing medicines to people around the world. We have vocations in South Africa.

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.