Reporting to the Clinical Operations Manager, you will be responsible for performing activities associated with start-up, initiation, monitoring and close out of clinical trials according to protocol, internal SOPs, ICH-GCP guidelines and related regulatory requirements. If you like a fast pace environment with loads of variety and challenges, then this is for you. Acting as the primary link between research sites and sponsors, your people skills will be highly sought after.
Your survival skills
You will need the following skills and attributes to assist you in succeeding in this role:
• At least 3-5 years’ experience working in the pharmaceutical industry/CRO
• Previous experience as a CRA on clinical trials in Australia or New Zealand
• Degree in Science or related healthcare discipline
• Sound knowledge of ICH-GCP guidelines, clinical trial conduct
• Ability to work autonomously with minimal supervision
• Great communication and client focus
• Passionate about the industry and being the best at what you do
• High attention to detail and problem solving initiatives
Send resume to tehreem@jobs-n-jobs.com or tehreemshah279@gmail.com
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