Regulatory Affairs Associate in Letchworth

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Established in 2005, the DLRC Group has developed a deserved reputation for being a leading consultancy, with a wealth of regulatory and scientific knowledge and considerable experience in both leadership and management. The company has recently expanded to include affiliates based in Germany and the US.

Our growing team comprises over 90 qualified professionals with a pharmaceutical and/or regulatory background, as well as over 30 dedicated supporting staff in areas of Business Development, Finance, Business Services and People Practices. We provide services to over 130 organisations, enabling them to achieve their strategic and operational development objectives.

DLRC’s expertise and flexible working approach ensures the provision of a highly motivated team who interact effectively with clients and regulators globally, to support both single issues and long‑term commitment to projects.

We are looking to offer recent graduates their first opportunity within Regulatory Affairs.

This role will be worked from our offices in Letchworth, UK until the probation period has been completed and then will be able to be operated on a hybrid basis.

Role Purpose: This role will support cross‑functional teams on company‑wide projects, including but not limited to business transformation, business development, training and people team initiatives. It will also support regulatory teams in working on assigned regulatory projects at various stages of development and post‑approval.

The closing date for applications is close of business on 1 January 2026. All applications will be reviewed internally, after which suitable candidates will be invited to an initial screening call during the week commencing 5 January 2026.

On‑site interviews for this role will take place on 29 January 2026, with an anticipated start date of 23 February 2026.

Responsibilities:

• Work on regulatory documentation alongside colleagues.
• Provide support for business development activities.
• Work alongside relevant stakeholders to analyse changes in the regulatory environment and legislation for impact on project plans and the overall business.
• Develop and give input to regulatory plans to meet project and client goals.
• Ensure relevant policies and procedures are in place and adhered to in order to meet the company’s legal responsibilities.
• Take responsibility for the oversight and completion of tasks within a project.
• Set appropriate milestones and monitor progress to deliver within set parameters.
• Identify and resolve issues proactively.
• Commit to deliver client and company requirements by demonstrating a willingness to help others outside the individual responsibilities.
• Share knowledge and keep stakeholders up to date with current project status.
• Adhere and follow DLRC behaviours and values for all work conducted at the company.

Qualifications:

• Life Science or Pharmacy Degree (or working towards one).
• Qualified to work in the UK.
• Fluent in English.
• Ability to work with an agile mindset showing flexibility and initiative whilst working cooperatively with others to achieve overall goals.
• Strong analytical skills: able to review large data sets and identify errors, inconsistencies and missing information.
• Able to clearly and confidently explain complex scientific issues both verbally and in writing.
• Strong attention to detail, receptive to ideas and feedback.
• Microsoft skills in particular PowerPoint and Excel (essential).