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Pharmacovigilance Associate (Dutch Language requirement) - Entry level and home-based in Europe, Guildford
Client: Location: Guildford, United Kingdom Job Category:
Other EU work permit required:
Yes Job Reference:
ea486cf976a5 Job Views:
7 Posted:
25.01.2025 Expiry Date:
11.03.2025 Job Description:
The PV Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry, biology, biotechnology, veterinary science, etc.). This is an opportunity for new graduates to start and develop their career within drug safety. The PV Associate will be working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. If you join PrimeVigilance, you can expect to work with teams of different sizes, from small clinical trials to large, generic post-marketing teams. We are always looking for proactive, capable, and motivated individuals who aim to surpass any target set in front of them. Responsibilities:
Processing of Individual Case Safety Reports from all sources (post-marketing and clinical trials) in compliance with applicable regulations, PrimeVigilance procedures, and in accordance with client-specific requirements and timelines, focusing on triage, data entry, quality review, and submissions workflow steps. Reconciliation activities for all types of received reports. Works under supervision and mentoring of more experienced colleagues. Qualifications:
We expect: Requirements:
Life science / biomedical background – healthcare related degree (chemistry, biology, biotechnology, veterinary science); previous experience is not required. People who are excited to learn and contribute to patient safety. Time and issue management, delegation, organization, and multitasking skills with good attention to detail. Strong interpersonal and communication skills. Advanced English skills and fluency in Dutch. Additional Information:
Why PrimeVigilance We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders, and ages can contribute and grow. To succeed, we must work together with a human-first approach. Why? Because our people are our greatest strength, leading to our continued success in improving the lives of those around us. We offer:
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. Our core values are key to how we operate, and if you feel they resonate with you, then PrimeVigilance could be a great company to join! Quality Integrity & Trust Drive & Passion Agility & Responsiveness Belonging Collaborative Partnerships We look forward to welcoming your application.
#J-18808-Ljbffr
Client: Location: Guildford, United Kingdom Job Category:
Other EU work permit required:
Yes Job Reference:
ea486cf976a5 Job Views:
7 Posted:
25.01.2025 Expiry Date:
11.03.2025 Job Description:
The PV Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry, biology, biotechnology, veterinary science, etc.). This is an opportunity for new graduates to start and develop their career within drug safety. The PV Associate will be working as part of a project team, performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. If you join PrimeVigilance, you can expect to work with teams of different sizes, from small clinical trials to large, generic post-marketing teams. We are always looking for proactive, capable, and motivated individuals who aim to surpass any target set in front of them. Responsibilities:
Processing of Individual Case Safety Reports from all sources (post-marketing and clinical trials) in compliance with applicable regulations, PrimeVigilance procedures, and in accordance with client-specific requirements and timelines, focusing on triage, data entry, quality review, and submissions workflow steps. Reconciliation activities for all types of received reports. Works under supervision and mentoring of more experienced colleagues. Qualifications:
We expect: Requirements:
Life science / biomedical background – healthcare related degree (chemistry, biology, biotechnology, veterinary science); previous experience is not required. People who are excited to learn and contribute to patient safety. Time and issue management, delegation, organization, and multitasking skills with good attention to detail. Strong interpersonal and communication skills. Advanced English skills and fluency in Dutch. Additional Information:
Why PrimeVigilance We prioritize diversity, equity, and inclusion by creating an equal opportunities workplace and a human-centric environment where people of all cultural backgrounds, genders, and ages can contribute and grow. To succeed, we must work together with a human-first approach. Why? Because our people are our greatest strength, leading to our continued success in improving the lives of those around us. We offer:
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. Our core values are key to how we operate, and if you feel they resonate with you, then PrimeVigilance could be a great company to join! Quality Integrity & Trust Drive & Passion Agility & Responsiveness Belonging Collaborative Partnerships We look forward to welcoming your application.
#J-18808-Ljbffr
