Clinical Research Assistant

At the moment we are looking forward to hire two persons for a Clinical Research Assistant position. Your responsibilities will include assisting Clinical Research Associates (CRAs) and project team members with site tasks (e.g. review of Case Report Forms and Study File Notebook, drug accountability) other administrative activities as required (e.g. payments to investigators, correspondence with clients, preparation of status reports, and organization of investigators’ meetings).

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 generation and reconciliation of queries to investigative sites/clients to resolve problem data.
• Assist with the management of study supplies and organize shipments.
• Create, update, track, and maintain study-specific trial management files, tools, and systems.
• Co-ordinate meetings with clients, investigators, and project team, including taking minutes.
• Ensure compliance with S.O.P.s, FDA, ICH, and GCP regulations for clinical conduct in all aspects of daily work.
• Provide input in writing Monitoring Conventions as assigned.
• Assist in submissions and notifications to Ethics Committees and Regulatory Authorities.

We Offer:
Covance's ongoing success offers team members unsurpassed growth and career development opportunities at an international organization; to pursue further training and to take advantage of our flexible conditions and attractive remuneration package
There is no better time to join us!

Covance is committed to diversity in the workplace and is an equal opportunity employer. (M/F/D/V). Your confidentiality and privacy are important to us.

To apply please visit our career site quoting the position name and the appropriate reference number - 38070BR.