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Pharmacovigilence Associate - German Speaking

Remote:

Full Remote

Experience:

Mid-level (2-5 years)

Work from:

United Kingdom

Offer summary

Qualifications:

Fluency in German and English, Minimum of 2 years Pharmacovigilance experience.

Key responsabilities:

Review, evaluate adverse event reports
Perform case processing activities
Conduct signal detection, prepare reports
Collaborate for accurate reporting
Support PV processes, team training

Luminary Group Startup https://luminarygroup.co.uk/

2 - 10 Employees

See more Luminary Group offers

Job description

Luminary Group is currently seeking a highly motivated and detail-oriented Pharmacovigilance Associate who is fluent in German 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 German and English, 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.