signatories to due dates Arrange training sessions, documenting training/registers and archive. Effective incorporate comments, tracking signatories, collecting training information, document implementation (effective customer feedback process. Ensuring external product training records are maintained. Medical Device File –
new products Training and Development Collaborate with Training Manager to enhance training program on continuous update Support Training Manager in developing content and conducting training sessions for new launches
activities, authoring local SOPs, conducting local training, and archiving and is able to perform these tasks May support PV Lead in maintaining the local PV Training matrix and onboarding plans. May support development e., Company Core Pharmacovigilance Documents, training materials, etc. as applicable) ensuring that they Responsible for completing all required/applicable trainings assigned at time of hire and after hire by the dates, before performing the activity. Supports training of local company staff, distributors, vendors
and Doctors within the region Providing weekly training sessions with pharmacists Meeting with key stakeholders
and Doctors within the region Providing weekly training sessions with pharmacists Meeting with key stakeholders
attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and Deliver training to sales forces and other departments; develop and update relevant training materials
attendance / participation at key internal meetings/training sessions, relevant congresses, and seminars and Deliver training to sales forces and other departments; develop and update relevant training materials
absence of the RP. Quality systems/SOPs drafting, training, maintaining and distribution. Product Release Conducting Risk Assessments. To implement and train on Quality systems, SOPs and GDP Pharmacovigilance
absence of the RP. Quality systems/SOPs drafting, training, maintaining and distribution. Product Release Conducting Risk Assessments. To implement and train on Quality systems, SOPs and GDP Pharmacovigilance
dossiers Tracking Regulatory Activity Internal training Assisting with internal product queries from relevant