Regulatory Affairs Professional
1 day ago
Randstad Life Science is seeking a highly skilled Regulatory Affairs Professional to join our team. As a key member of our global team, you will be responsible for ensuring efficient and seamless Regulatory Information Management across all stages. Your expertise in areas vital to successful RIM execution will enable us to stay ahead in the dynamic world of pharmaceuticals.
About the Role:
We are looking for a talented individual with a strong understanding of the pharmaceutical drug development process. You will work closely with teams to ensure alignment with industry standards, regulatory requirements, and business processes. Your analytical and critical thinking abilities will be essential in preparing and submitting regulatory data submissions to health authorities.
Responsibilities:
- Collaborate with teams to ensure efficient and seamless Regulatory Information Management.
- Oversee the regulatory data for assigned areas, ensuring alignment with industry standards, regulatory requirements, and business processes.
- Prepare and submit regulatory data submissions (XEVMPD, IDMP, etc.) to health authorities.
- Continuously develop expertise in areas vital to successful RIM execution, with a focus on technical skills and international regulations.
- Engage with partners, affiliates, and stakeholders to manage regulatory data and ensure adherence to standards and procedures.
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