Luminary Group is a Global Executive Search and Headhunting business specialising within the Life Sciences and Pharmaceutical space, headquartered in Broadgate Tower, 20 Primrose Street, EC2A 2EW, London. Finding premium candidates globally. We specialise in the Pharmaceutical, Biotechnology, CDMO, CRO & Medical Devices disciplines with local expertise and specialist knowledge. Specifically headhunting candidates for specialist roles across Board, Executive, Commercial, Operations, Medical, IT and Finance. With global coverage across USA, Europe, APAC, and Middle East, we pride ourselves in both our outstanding talent pool (ranging from C-Suite to Manager level) and our returning clients who work with us exclusively. Partnered with the best, and most exciting, companies ranging from Corporate to Start-Up businesses. We are Luminary. You are Luminary.

Job description

Luminary Group is currently seeking a highly motivated and detail-oriented Pharmacovigilance Associate with fluency in multiple European languages to join our team. As a Pharmacovigilance Associate, you will play a crucial role in monitoring and ensuring the safety and efficacy of our client's pharmaceutical products.

Responsibilities:

Review and evaluate adverse event reports and other safety-related information for our client's products.
Perform case processing activities, including data entry, coding, narrative writing, and quality checks.
Conduct signal detection activities and contribute to the preparation of signal evaluation reports.
Collaborate with cross-functional teams to ensure timely and accurate reporting of adverse events to regulatory authorities.
Participate in the development and implementation of Pharmacovigilance processes and procedures.
Assist in the training and mentoring of junior team members.
Maintain knowledge of current regulatory requirements and guidelines related to Pharmacovigilance.
Ensure compliance with company policies and standard operating procedures.
Contribute to the continuous improvement of Pharmacovigilance activities and systems.

Requirements

Fluency in multiple European languages, both written and spoken.
Minimum of 2 years of experience in Pharmacovigilance or a related field.
Strong knowledge of Pharmacovigilance practices and regulations.
Experience with case processing activities, including data entry, coding, and narrative writing.
Proficiency in using Pharmacovigilance databases and safety reporting systems.
Ability to work independently and prioritize tasks effectively.
Excellent attention to detail and accuracy in data entry and documentation.
Strong analytical and problem-solving skills.
Good interpersonal and communication skills, with the ability to effectively collaborate with cross-functional teams.
Experience with MedDRA coding and EudraVigilance is desirable.
Flexibility to work in different time zones, if required.