Local Qualified Person for Pharmacovigilance
Job Fit Check
Base Career helps you apply smarter for this job.
Key skills for this role
About the Role
Essential Functions Maintain the local PV system compliant, according with local Legislation and GVPs. Work closely with project teams to determine appropriate terms and conditions of safety agreements.
Key Skills for This Role
Full Job Posting
Essential Functions
- Maintain the local PV system compliant, according with local Legislation and GVPs.
- Work closely with project teams to determine appropriate terms and conditions of safety agreements.
- Act as primary point of contact or deputy on assigned projects and manage the pharmacovigilance agreement development process for large, complex projects and provide support as required.
- Act as primary customer interface on large, complex projects, responsible for maintaining and developing customer relationships.
- Customize project documents to accurately reflect services provided. Oversee finalization and distribution of documents.
- Assist in the negotiation of safety agreement text using approved procedures and templates.
- Create safety agreements as required, review complex agreements and provide guidance and advice to team.
- Prepare and maintain PSMFs and PSSFs.
- Reviews PSMFs prepared by other specialists.
- Provide advice, support and guidance to other staff as needed.
- Perform all other duties as assigned
Qualifications
- Bachelor's Degree in health science.
- 2 years experience in a Contract Research Organization or Pharmaceutical company including at least 1 years of Lifecycle Safety experience (Local contact person for Pharmacovigilance, PSMF and PSSF management, PVA, Aggregate reporting, Risk Management, etc). Equivalent combination of education, training or experience.
- Excellent knowledge of Lifecycle Safety processes.
- Excellent attention to detail and accuracy and maintain consistently high quality standards.
- Excellent written and verbal communication skills.
- Effective mentoring skills.
- Ability to work effectively on multiple projects simultaneously.
- Organize own workload and effectively time manage competing priorities.
- Ability to establish and maintain effective working relationships with co-workers’, managers and clients.
- IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.
- We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.
- Learn more at https://jobs.iqvia.com
- IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud.
- All information and credentials submitted in your application must be truthful and complete.
- Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law.
- We appreciate your honesty and professionalism.
Apply for this job in 1 click
Skip the repetitive application forms
Install the Base Career Chrome Extension and autofill job applications across major job boards with your profile.
Trusted by over 500,000 job seekers on Base Career
More from this employer
More jobs at IQVIA
Analyste en technologies / Technology Analyst
Kirkland, CAN
IQVIA seeks a Technology Analyst to join its Canadian Technology team, working with life sciences clients on data analytics, technology solutions, and client relationship management. The role requires 1-3 years of experi
Junior Clinical Research Associate Sponsor-dedicated
Riyadh, KSA
IQVIA seeks a Junior Clinical Research Associate to perform monitoring and site management for clinical studies. The role involves site visits, subject recruitment tracking, and ensuring compliance with GCP/ICH guideline
Junior Clinical Research Associate Sponsor-dedicated
الرياض, KSA
Job Overview Perform monitoring and site management work to ensure that sites are conducting the study(ies) and reporting study data as required by the study protocol, applicable regulations and guidelines, and sponsor r
Patient Support Programs - Senior Consultant
Riyadh, KSA
IQVIA is seeking a Senior Consultant for Patient Support Programs in Riyadh. The role involves project management, client analysis, and program design for patient support in the life sciences field. Requires a Bachelor's
Patient Support Programs - Senior Consultant
الرياض, KSA
IQVIA seeks a Senior Consultant to lead patient support programs in the life sciences field. The role involves project management, client collaboration, and program design for the largest PSP program in the region. Requi
Patient Coordinator
Dubai, UAE
IQVIA is seeking a Patient Coordinator to support project managers and project teams in clinical research. The role involves assisting with project documentation, database management, reporting, meeting coordination, and
Patient Coordinator
Dubai, UAE
IQVIA is looking for a Patient Coordinator to provide support to project managers and project teams. The role requires a graduate degree in healthcare or medical background, fluency in Arabic and English, and 2-3 years o
Site Activation Specialist
Dubai, UAE
IQVIA seeks a Site Activation Specialist to manage clinical research site activation activities in Dubai. The role involves regulatory submissions, contract negotiation, and project coordination. Requires a life science
Analyste en technologies / Technology Analyst
Kirkland, CAN
Junior Clinical Research Associate Sponsor-dedicated
Riyadh, KSA
Junior Clinical Research Associate Sponsor-dedicated
الرياض, KSA
Patient Support Programs - Senior Consultant
Riyadh, KSA
Patient Support Programs - Senior Consultant
الرياض, KSA
Patient Coordinator
Dubai, UAE
Patient Coordinator
Dubai, UAE
Site Activation Specialist
Dubai, UAE