Chiltern International has added to its regulatory department with the appointment of Sharon Rouse as regulatory affairs officer
Clinical research organisation Chiltern International has added to its regulatory department with the appointment of Sharon Rouse as regulatory affairs officer.
A pharmacist by profession 25 years of experience in the pharmaceutical industry, Rouse will be responsible for the compiling and submission of clinical trial applications and marketing authorisations for Chiltern and will also assume responsibility for pharmacovigilance reporting.
She brings with her a rich background of experience, which includes running her own business for 15 years and expertise running a hospital pharmacy in Zimbabwe, developing systems and procedures to control and co-ordinate the pharmacy services and stocks throughout the hospital.
Rouse has also worked in the pharmaceutical manufacturing industry as a quality assurance director of a pharmaceutical manufacturing company with responsibility for quality assurance and regulatory affairs.
Her work spread across many African countries, including South Africa, Malawi, Namibia, Zambia, Botswana, Tanzania and Zimbabwe. Looking forward to her hew role based at Chiltern International's Slough headquarters, Rouse commented: "Working and living in Africa certainly put my skills to the test and I hope this will be of value to Chiltern International. "Clinical research is a new and exciting area for me and I hope to learn from it as well as be able to utilise the experience and skills I have gained over the years."
