Riham Elbadri

Clinical Drug Safety Lead

Case processing and data entry of single case report data into ARISg® Safety Database for clinical trials and post-marketing projects. Responsible for case submissions and data entry into the eudravigilance gateway. Generation of single case regulatory reports as well as Line Listings to ensure regulatory compliance. Submissions of regulatory SUSAR, periodic and cross-reports to Competent Authorities, Ethics Committees and investigational sites

Responsible for developing business opportunities with different health professionals by introducing new products to key clients. Organizing conferences for doctors and other medical staff to Increase the awareness and use of the company's pharmaceutical and medical products. Acquired presentation skills by presenting and discussing clinical data to support the brand drugs supplied by the company with health professionals. Increase the awareness and use of their company's pharmaceutical and medical products

Dispensing prescription medicines to the public. Ensuring that different treatments are compatible. Checking dosage and ensuring that medicines are correctly and safely supplied and labelled. Keeping a register of controlled drugs for legal and stock control purposes. Liaising with doctors about prescriptions. Counseling and advising the public on the treatment of minor ailments. Advising patients of any adverse side-effects of medicines or potential interactions with other medicines/treatments

Masters in molecular life sciences Specialization in cellular and molecular biology Specialization in molecular genetics