Office based Study Operations role with Blue Chip company now open
Do you want to gain exceptional experience working within a leading team? Do you want to work for an International pharma who have expertise in Cardiovascular, Oncology, Inflammation and Infectious Disease? If so then please read on for your opportunity to progress your career.
Our client, is looking to recruit a Senior CRA/Scientist Specialist to be responsible for global planning and oversight activities in the running of regulatory and marketing clinical studies. The role allows you to relinquish site management and focus on coordination and contribution to Study Delivery activities that ensure quality, consistency, and integration of study data and progress deliverables to time cost and quality parameters. You could work in any arena from Study Design Concept to database lock and study close-out activities
This role would suit candidates who have relevant industry or health related experience, an understanding of the clinical study and drug development process and GCP, and those who have proven organisational skills and are keen to work within a demanding environment
This is a contract to work full time at their offices based in the client office in the North West. Part time applications and home based working is not possible. The contract duration for 11 months.
CSL have staff assigned in this role and know the team well. If you would like more information I would be happy to forward on^the full job description. If this role is not of interest please send to anyone who might be suitable.
Term of of Employment with CSL:
CSL offer candidates a payroll of umbrella employment option.
Keywords:
Midlands, Loughborough, Clinical,site management, study design, GCP, pharmaceutical, drug development, study delivery, Senior CRA. CRA, cardiovascular, oncology.