Safety Data Specialist
7 dni temu
We're excited to announce the opening of a new role within our pharmacovigilance team in Warsaw.
This is an exciting opportunity for a highly motivated and organized individual to join our team and contribute to the success of our clients.
The successful candidate will be responsible for supporting the collection, documentation, and reporting of safety data related to medications and clinical trials.
Key Responsibilities:
- Supporting the collection, review, and processing of adverse event reports related to clinical trials and marketed products.
- Ensuring timely and accurate data entry of safety information into pharmacovigilance databases.
- Assisting in the preparation and submission of safety reports to regulatory authorities and sponsors, as required.
- Collaborating with cross-functional teams to maintain compliance with safety regulations and company protocols.
- Maintaining detailed records and documentation related to pharmacovigilance activities and safety reporting.
Requirements:
- Bachelor's degree in life sciences, pharmacy, or a related field.
- An understanding of pharmacovigilance principles and regulatory requirements is preferred.
- Strong attention to detail and organizational skills, with the ability to manage multiple tasks efficiently.
- Effective communication and collaboration skills, with a focus on maintaining accuracy in documentation and reporting.
- Ability to work in a fast-paced, regulated environment, ensuring compliance with safety guidelines and protocols.
- Role is office based (with option of 2 days at home). This is not negotiable.
About Us:
Our mission is to deliver exceptional value to our clients by combining our expertise in clinical research and drug development with innovative technology solutions.
We're passionate about driving innovation and improving outcomes for patients around the world.
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