Jobb som matchar luminary group
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6 jobb
- Luminary GroupDistansjobb·
- As a Pharmacovigilance Associate, you will play a crucial role in monitoring and ensuring the safety and efficacy of our client's pharmaceutical products.
- Luminary GroupDistansjobb·
- We are seeking a visionary leader who can drive strategic initiatives, build strong client relationships, and deliver exceptional consulting services.
- Luminary GroupDistansjobb·
- As a Pharmacovigilance Associate, you will play a crucial role in monitoring and ensuring the safety and efficacy of our client's pharmaceutical products.
- Luminary GroupDistansjobb·
- As a Business Development Director for Real World Evidence, you will be responsible for developing and executing a strategic business development plan,…
Visa liknande jobb hos den här arbetsgivarenLuminary GroupDistansjobb·- As a Business Development Director, you will be responsible for driving new business opportunities and expanding our client base within the life science…
- Luminary GroupDistansjobb·
- As a Business Development Director, you will be responsible for driving new business opportunities and expanding our client base within the life science…
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Job Post Details
Pharmacovigilence Associate - Swedish, Danish, Norwegian Speaking
Luminary Group
Distansjobb
Fullständig jobbeskrivning
Luminary Group is currently seeking a highly motivated and detail-oriented Pharmacovigilance Associate who is fluent in Swedish, Danish, and Norwegian 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::
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.
- Fluency in Swedish, Danish, and Norwegian, 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.
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