Pharmacovigilance Professional

3 semanas atrás


Lisboa, Lisboa, Portugal PrimeVigilance Tempo inteiro

We are seeking a highly skilled Pharmacovigilance Professional to join our team at PrimeVigilance. As a key member of our project team, you will be responsible for managing case processing services with full accountability.

Job Description

In this role, you will work independently to process Individual Case Safety Reports from various sources, including post-marketing and clinical trials, in compliance with applicable regulations and client specific requirements. You will also manage SAE/SUSAR submissions, unblinding, and clinical trial reconciliations, as well as prepare database outputs for periodic reporting.

You will have the opportunity to mentor and train new employees within the department, including procedure optimization and development. Your strong interpersonal and communication skills will enable you to effectively collaborate with colleagues worldwide.

Required Skills and Qualifications
  • A life science or biomedical background, with a healthcare-related degree such as chemistry, biology, biotechnology, or veterinary science.
  • Demonstrated experience in pharmacovigilance case processing.
  • Excellent time and issue management, delegation, organization, and multitasking skills, with a keen eye for detail.
  • Strong English language skills, both verbal and written, at a C1 level.
Benefits

We offer a competitive salary range of $80,000 - $110,000 per annum, depending on location and experience. Additionally, we provide training and career development opportunities, a friendly and supportive working environment, and the chance to work with colleagues from diverse backgrounds worldwide.

Our core values include quality, integrity and trust, drive and passion, agility and responsiveness, belonging, and collaborative partnerships. If these values resonate with you, PrimeVigilance could be an ideal company to join.


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