Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring? Our team says it’s the best of both worlds….ClinChoice is searching for a Senior Area/Local Safety Officer Full Time Role to join one of our clients.Hybrid Model: 2-3 days a weekLanguage: The contractor must be fluent in English and have Spanish as a mother tongue.Job DescriptionSenior Area Safety Officer, Local PV Spain and Southern EuropeThis position reports into Area Safety Head and is based in Madrid, SpainPOSITION SUMMARY:The Senior Area Safety Officer is responsible for ensuring that the local operating company (LOC) Safety activities related to all products are managed in compliance with local regulations and company policies/ procedures at a local, regional, and global levels and in accordance with any product vigilance agreements with third party business partners. This role might act as the LOC’s and assigned territories main point of contact for pharmacovigilance matters (including cosmetovigilance, materiovigilance and nutrivigilance) with the local health authority.They will ensure that appropriate product vigilance and risk management systems are set in place to assure appropriate oversight of products within its responsibility.PRINCIPAL RESPONSIBILITIES:Oversight of the PV System & Overall responsibilitiesProvide oversight of vendor resources within Spain, Andorra, Italy, San Marino, Vatican City, Portugal, Greece and Cyprus.Support the Area Safety Head in providing relevant local information for the European Economic Area Pharmacovigilance System Master File.Record self-identified non-conformances and collaborating with the global team to investigate non-conformances while developing and implementing effective Corrective and Preventative Actions (CAPAs).Safety Management & ReportingReceive and support the Area Safety Head in the responses to safety-related health authority queries.Perform reconciliation with other departments (distributors, third parties, vendors, and internal stakeholders).Maintain oversight of proper identification of local literature articles for Adverse Event (AE) reporting as required.Perform document management and archiving as required.Ensure proper documented training on safety reporting responsibilities of LOC personnel and maintenance of awareness of safety reporting in general.Perform regulatory monitoring for impact on vigilance activities and responsibilities.Collaborate with the global and local teams to notify local health authorities of any safety issues including SSI/ESI and Signals.Manage reporting/ submissions of safety reports/ updates/information (e.g., SAE, SUE, SUSARs, PSUR, RMP) to local health authorities and other departments as applicable.Maintain up-to-date knowledge of local requirements for pharmacovigilance, cosmetovigilance, materiovigilance and nutrivigilance, including reporting requirements (for all applicable product classes in the territory) and collaborating with the global team to implement process changes required for identification of new requirements.Ensure pharmacovigilance compliance of local company sponsored programs and research activities as applicable.Perform translation for ICSR and PV-related documents, as required.Provide technical and strategic input and participate in projects/ workstreams led by the Medical Safety teams or LOC.Procedural DocumentDevelop, update, and implement local procedures to ensure compliance with global procedures and national requirements.Ensure current knowledge of all relevant company procedures and training.Audit & inspection readinessSupport local health authority inspections and audits conducted locally, including responding to queries during the conduct and collaborating with the global team to develop and implement CAPA plans as applicable.Vigilance contract managementManagement of vigilance contracts and clauses: set-up, revision, internal tracking and periodic reconciliations.Business ContinuityEnsure implementation of local business continuity plans (e.g., inspection readiness, AE reporting coverage).Qualifications:The minimum knowledge, skill, related experience, and ability requirements for the position.Education:Health care science professional e.g.: (Pharmacist, nurse…)Years of Related Experience:At minimum 3 years’ experience.Knowledge, Skills, Abilities:Pharmaceutical industry experience including product vigilance responsibility role.Proven ability to organize workflow activities.Computer literate with knowledge of relevant IT safety systems.Good verbal and written communication skills.Ability to establish and maintain open relationships within the organization and with authorities.Demonstrable knowledge of local requirements and global aspects of product safety.Mother tongue: SpanishFluency in the English language is required.Key words: PSMF, PSSF, PV, Pharmacovigilance, Regional LeadApply for this job*indicates a required fieldFirst Name *Last Name *Email *PhoneCountry *Phone *Location (City) *Resume/CV *Enter manuallyAccepted file types: pdf, doc, docx, txt, rtfEnter manuallyAccepted file types: pdf, doc, docx, txt, rtfEducationSchool * Select...Degree * Select...Select...Start date year *End date yearLinkedIn ProfileWebsiteCountry * Select...Enter country of residenceAre you legally authorized to work in the country that you are being hired? * Select...If "yes", will you now or in the future require sponsorship to work in the country that you are being hired? * Select...Have you previously worked for ClinChoice or its subsidiaries? 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I understand any false information or omission may disqualify me from further consideration for employment and may result in my dismissal if discovered at a later date.I understand that an offer of employment may be contingent on verifying the statements contained in this application (e.g., evidence of a qualification).I understand that an offer of employment is contingent on receipt of satisfactory references.I understand an offer of employment may be contingent upon successful completion of a background check. 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