
Regulatory and Pharmacovigilance Specialist – Network
ERGOMED
full-time
Posted on:
Location Type: Remote
Location: United Kingdom
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About the role
- Provide the strategy based on regulatory requirements and for completing regulatory and PV deliverables based on an established PV and regulatory plan
- Serve as a liaison between regulatory and other functional areas including external partners, clients, authorities and/or consultants in the planning, organizing, and preparing of regulatory deliverables following project, corporate and industry regulatory strategies
- Act as Local Contact Person for Pharmacovigilance for the designated country
- Assume leadership and functional representation for projects of low complexity assigned ensuring effective and rapid coordination and management of deliverables striving the team to meet the agreed targets and to comply with the agreed procedures, trackers and templates
- Provide intelligence on requirements and contribute to the development of the strategy and set up activities (Project Management Plan, joint operating procedures, POAs and core documents)
- 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 identify and escalate risk/potential risk to the project team which may jeopardise deliverables
- Provide Clients expertise and guidance at national level
- Maintain awareness of allocated tasks and hours and promptly identify and escalate any OoS
- Prepare client’s invoices and review/ approve vendors’ project invoices
- Provide support to proposal development and input to budgets, provide department representation to BD meetings as required
- Foster professional working relationships with internal and external contacts at the local and international levels to ensure smooth and efficient service delivery
- Stay abreast of changing regulatory legislative requirements and ensure maintenance of the regulatory intelligence database and timely dissemination of pertinent changes
- Participate in preparation for audits/inspections and provide department representation for assigned projects as required
- Track LCPs' key performance indicators and prepare monthly summary reports
- Provide feedback on performance of vendors to aid their assessment
- Communicate suggestions for changes to departmental/company processes/procedures
Requirements
- 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
Benefits
- 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
Applicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
PharmacovigilanceProject ManagementRegulatory ComplianceRisk ManagementData AnalysisPerformance TrackingInvoice ManagementTraining ComplianceRegulatory IntelligenceAudit Preparation
Soft Skills
LeadershipInterpersonal SkillsOrganizational SkillsAttention to DetailCommunication SkillsProblem SolvingClient ManagementTeam CoordinationAdaptabilityStrategic Thinking
Certifications
Bachelor's Degree in ChemistryBachelor's Degree in Life SciencesBachelor's Degree in NursingPharmacovigilance Training