Principal Regulatory/Medical Writer

Apsida Life Science is partnering with a long-standing client, a well-established regulatory writing consultancy that has been delivering strategic support to global pharmaceutical organisations for over 20 years. Comprised of experienced scientific and regulatory specialists, the team helps clients navigate complex regulatory challenges and critical decision-making throughout the product lifecycle.

Renowned for their scientific excellence, collaborative culture, and strategic expertise, the organisation offers the opportunity to work across a diverse portfolio of projects spanning a wide range of therapeutic areas.

As part of their continued growth, they are now seeking a Principal Regulatory Writer based in Canada or the US to play a key role in expanding their presence and supporting clients across the North American market.

Please note: this role offers the possibility of a 0.8 FTE working model.

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