Regulatory Affairs Director
hace 3 días
At Worldwide Clinical Trials, LLC, we are seeking a highly skilled Regulatory Affairs Manager to join our team. As a key member of our regulatory team, you will be responsible for ensuring compliance with regulatory requirements and guidelines.
Key Responsibilities:
- Review and manage regulatory submissions and approvals across EMEA, Asia Pacific, and Latin America regions.
- Provide expert regulatory advice and contribute to regulatory project work.
- Coordinate and manage regulatory and ethics committee submissions.
- Develop and maintain relationships with regulatory agencies and stakeholders.
Requirements:
- Minimum 7 years of experience in the pharmaceutical or CRO industry, with a focus on regulatory affairs.
- Proven leadership and organizational management skills.
- Excellent written and verbal communication skills.
- Ability to work in a fast-paced environment and prioritize multiple tasks.
About Us:
Worldwide Clinical Trials, LLC is a leading global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new medications from discovery to reality.
We are united in our cause to improve the lives of patients through new and innovative therapies. Our talented team of 3,000+ professionals spans 60+ countries, and we are committed to enabling professionals from all backgrounds and experiences to succeed.
We prioritize cultivating a diverse and inclusive environment that promotes collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.
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