£50K/yr to £70K/yr
England, United Kingdom
Contract, Variable

Clinical Trial Regulatory Specialist

Posted by Consult .

Hybrid working 2x a week

Scope:

This is an excellent opportunity for an experienced Clincial Trial Regulatory Specialist to join a global pharmaceutical company for an initial 12 months with the potential for this to be extended. This role has come about due to expansion and an increase in the production of pharmaceutical. They are looking for someone with at around 2 years of CTS. This is a supportive role looking at completion of company databases and submissions tracking and would suit someone who is looking to get experience of the pharmaceutical industry, particularly regulatory affairs within clinical trials.

Responsibilities:

  • Oversee a portfolio of CTAs, managing the preparation and dissemination of documentation for new initial CTAs and all CTA maintenance activities, including substantial amendments and end-of-trial notifications.
  • Offer guidance on submission strategy, country-specific requirements, and operational assistance for Regulatory submission preparation and processing of amendments.
  • Ensure adherence to approved company CTA processes within established timelines.
  • Demonstrate a thorough understanding of the Clinical Trial Regulation (CTR) process and its requirements.
  • Track key project milestones, compare actual progress with planned activities and timelines, and communicate any issues or changes to relevant stakeholders and management in accordance with company procedures.
  • Populate relevant databases and activity trackers within agreed timelines, ensuring compliance with reporting requirements, and provide operational support for Regulatory and/or non-Regulatory systems critical for Regulatory submission and maintenance activities.

About You:

  • Minimum 2 years of CTA experience, with a preference for involvement in global clinical trial submissions to regulatory agencies.
  • Demonstrated ability to work effectively across diverse cultures and within complex matrix environments.
  • Proficient in Information Technology, including MS Word, Excel, PowerPoint, Adobe Acrobat, and global databases.
  • Proactive communication style, both written and verbal, with a solution-driven approach.
  • Exhibits high levels of initiative and independence, along with strong interpersonal skills and the ability to establish and maintain working relationships across remote geographical locations.