Senior Regulatory Affairs Specialist

1 month ago


Manchester, United Kingdom Planet Pharma Full time
Senior Regulatory Affairs Associate

Planet Pharma is seeking a highly skilled Senior Regulatory Affairs Associate to join our team on an initial 12-month contract with potential for extension.

Key Responsibilities:

  • Develop and execute regional regulatory strategies and plans to ensure compliance with regulatory requirements.
  • Prepare and manage regulatory deliverables, including clinical trial applications, marketing authorizations, and lifecycle management activities.
  • Utilize Amgen systems and document management to ensure efficient and seamless execution.
  • Ensure regulatory product compliance and support the development of policies and SOPs.
  • Build and maintain effective relationships with local and functional organizations to drive business growth.
  • Enable regional countries to execute efficiently and effectively.

Key Requirements:

  • Bachelor's or Master's degree in a scientific field.
  • At least 2 years of direct relevant experience.
  • Clinical trials experience is preferred.

About Planet Pharma:

Planet Pharma is a global staffing services company with a strong presence in the pharmaceutical industry. We provide expert recruitment solutions to clients across the globe, with a focus on regulatory affairs, pharmacovigilance, and quality assurance.

We are committed to excellence and service delivery, and have received recognition from industry bodies for our achievements. Our team is dedicated to helping clients find the best talent for their needs, and we welcome applications from all suitably qualified candidates.



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