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We are seeking a highly skilled and motivated professional to join our team as a Senior Drug Safety Associate.
About the RoleThis is an exciting opportunity to work in a dynamic environment where you will be responsible for preparing regulatory documentation packets and coordinating the timely completion and submission of required reports to health authorities, ethic committees, principal investigators, and business partners.
Key Responsibilities- Ensure compliance with regulatory reporting requirements for safety reporting in clinical trials.
- Ensure all sponsor and regulatory timeframes are met for the reporting of safety information.
To succeed in this role, you will need excellent communication and organizational skills, as well as the ability to work effectively in a team environment. You will also need to have a strong attention to detail and be able to meet deadlines in a fast-paced environment.
What We OfferWe offer a comprehensive and competitive total reward package that comprises an excellent level of base pay, variable pay, and recognition programs. We also offer best-in-class employee benefits, supportive policies, and wellbeing initiatives tailored to support you and your family at all stages of your career.
