Provide the strategy based on regulatory requirements
Complete regulatory and PV deliverables based on an established PV and regulatory plan
Serve as a liaison between regulatory and other functional areas
Assume leadership and functional representation for projects of low complexity assigned
Provide intelligence on requirements and contribute to the development of the strategy
Support identification of issues and corrective actions
Collect, review, track and maintain LCPs' CVs, job descriptions, training records, contact details and monthly reports
Ensure correct training assignment to and training compliance by the LCPs
Promptly identifying and escalating risk/potential risk to the project team
Prepare client’s invoices and review/ approve vendors’ project invoices
Foster professional working relationships with internal and external contacts
Stay abreast of changing regulatory legislative requirements
Participate in preparation for audits/inspections

Bachelor's Degree in Chemistry or Life Sciences, Nursing, or equivalent experience
Previous experience within the pharmaceutical/CRO industry
PV training and/or working experience and other educational or professional background as required locally
Fluent in English, both written and verbal
Candidate must be proficient in the official language of the country in which they are based, as this is essential for local interactions and compliance.
Good planning and organizational skills
Strong interpersonal skills in a fast-paced, deadline oriented, and changing environment
Good attention to detail

Training and career development opportunities internally
Strong emphasis on personal and professional growth
Friendly, supportive working environment
Opportunity to work with colleagues based all over the world, with English as the company language

Specialist, Regulatory and Pharmacovigilance Network

Key skills