Senior Consultant

My client are a highly successful Regulatory Affairs Consulting Practice. They serve the Pharmaceutical and Biotechnology industries, from early stage product (drug) development through to marketing approval. They have a great culture, excellent values, a very supportive team and significant growth plans for 2023.

Please note to be considered for this role you **must have require the right to work in the UK - sponsorship cannot be provided** for this role.

We are seeking a highly motivated individual for the role of a **full-time Senior Consultant with a Clinical/Regulatory Affairs focus.**

You will be providing high quality, clinical, regulatory technical advice and product development strategies to a portfolio of clients as part of a global team.

Their office base is on the **Herts/Essex** border. This role offers **hybrid working **and the expectation is a **minimum of 2 - 3 days **per week in the office.

An excellent command of the English language, written and verbal, is required for this role.

For more information please send your CV (including your contact details) and covering letter outlining your experience as soon as possible and I will be in touch with you.

**Job Types**: Full-time, Permanent

**Salary**: £60,000.00-£80,000.00 per year

**Benefits**:

- Company events
- Company pension
- Private medical insurance
- Profit sharing
- Work from home

Schedule:

- Day shift
- Monday to Friday

Supplemental pay types:

- Bonus scheme
- Performance bonus
- Yearly bonus

Ability to commute/relocate:

- Stansted: reliably commute or plan to relocate before starting work (required)

Application question(s):
**Experience**:

- pharmaceutical or relevant service provider: 5 years (required)
- Regulatory Affairs: 5 years (required)

Work authorisation:

- United Kingdom (required)

Work Location: Hybrid remote in Stansted

Reference ID: SEE09022023SC
Expected start date: 01/03/2023