Responsible for Information and Publicity Pharma (RIP) for a pharmaceutical company
Main duty: ensuring the compliance to national regulations and global procedures related to information, advertising and medical samples management.
Department: Regulatory affairs
· Providing the annual registry of medical samples.
·Redaction of the abridged SPC and safety pages and control of translations.
·Create/update all the relevant local standard operating procedures (SOP) and training all collaborators about it.
·Evaluate all promotional and informative materials and give approval (or refusal) before use.
·Take part of the management of any complaint and their follow-up related to promotional activities (IN & OUT).
·Validate all scientific events/meetings/sponsoring not subject to MDeon Visa
·Maintain registers of all promotional and informative materials and scientific events
·Perform training for Marketing/Promotion (including medical reps) staff.
·Perform regular spot checks in the following matters :
i. Scientific events/congresses/sponsoring subject to MDeon Visa
ii.Premiums or benefits offered to health care professionals
iii.Medical sample and management tool
iv. Annual spot check of training department
v.Annual spot check of the medical or scientific information request given by SIM
·Ensure to fulfill all the transparency‘s obligations defined by the Royal Decree of 14 June 2017 related to the Sunshine Act.
·Act as Compliance relay for the HQ.
·Manage Jr. legal and compliance officer.
·Ensure all the implementations from HQ’s policies, directives and guidelines into local procedures.
· Act as Data Protection Officer (as defined by the GDPR entered into force from May 25th 2018).
·Provide support to business operations concerning compliance issues.
§ Diploma of Pharmacist or Medical Doctor,
§ RIP agreement number,
§ Analytical and communication skills,
§ Well-organized, rigorous, autonomous
open-ended contract with interesting advantages