Position Summary: The incumbent is responsible for supporting Pharmacovigilance-related activities in South scope of the role and the countries the role will support, includes, Sub Saharan Africa (Angola, Botswana Therapeutic Areas, and Disease Pathway knowledge supporting the needs of the local Medical and Marketing regulations. Pharmacovigilance-Safety training support: Support LSO/CSTL in the preparation, conduct and timely material, where needed. PV contract management: Support LSO/CSTL with the local Pharmacovigilance Agreements
Position Summary: The incumbent is responsible for supporting Pharmacovigilance-related activities in South scope of the role and the countries the role will support, includes, Sub Saharan Africa (Angola, Botswana Therapeutic Areas, and Disease Pathway knowledge supporting the needs of the local Medical and Marketing regulations. Pharmacovigilance-Safety training support: Support LSO/CSTL in the preparation, conduct and timely material, where needed. PV contract management: Support LSO/CSTL with the local Pharmacovigilance Agreements
nuclear gauges are involved. Laboratory Operations Support Act as a Professional as per the Codes of Ethics gauges are involved. Quality Systems Support Maintain and support the ISO 17025:2017 accreditation. Train quality management processes. Project Specific Support Participate and assist with Drafting and Reviewing
nuclear gauges are involved. Laboratory Operations Support Act as a Professional as per the Codes of Ethics gauges are involved. Quality Systems Support Maintain and support the ISO 17025:2017 accreditation. Train quality management processes. Project Specific Support Participate and assist with Drafting and Reviewing
non-conformity
pharmaceutical company to apply. The role is to support and assist the Regulatory Affairs pharmacists with
pharmaceutical company to apply. The role is to support and assist the Regulatory Affairs pharmacists with
participants according to study schedule
Required
participants according to study schedule
Required
study participants according to study schedule Support data extraction from clinic registers, patient in-depth interviews with recruited study participants Support data capture and data quality control on sites patients and caregivers Participate, give input, and support ad hoc projects and initiatives Required minimum