European Regulatory Strategist

CK Group; Walton On The Hill; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A leading biopharmaceutical company is seeking an experienced European Regulatory Strategist to develop and implement regulatory strategies. The role involves ensuring timely submissions and optimal interactions with health authorities. Candidates should possess a relevant scientific degree and previous experience in regulatory liaison. This is a hybrid role based in Walton On The Hill, UK, on a contract basis for 10 months, offering competitive pay rates.

Qualifications

• Previous experience as a national and/or regional regulatory liaison for at least one product in different therapeutic areas.
• Experience in communicating with regulatory authorities at various stages of the product life cycle.

Responsibilities

• Ensure optimal regulatory interactions with Health Authorities.
• Communicate progress and variances to the Global Regulatory Lead and Senior Management.
• Ensure business compliance with regulatory standards.

Skills

Lead and implement regional regulatory strategies

Accountable for timely submissions and approvals

Knowledge of drug development practice rules

Experience in communicating with FDA or major EU regulatory agencies

Proven ability in developing and implementing regulatory strategy

Education

Relevant scientific degree or equivalent working experience

Job description

European Regulatory Strategist

CK Group are recruiting for a European Regulatory Strategist to join a company in the pharmaceutical industry on a contract basis for 10 months. This will be working hybrid with 2 / 3 days per week at the clients site in Tadworth.

Salary :

Up to £33.78 ph PAYE or £37.86 ph via umbrella company.

European Regulatory Strategist Role

• European Regulatory Strategist
• Lead and implement regional regulatory strategies
• Accountable for timely submissions and approvals, and ensuring optimal regulatory interactions with Health Authorities
• Ensures regulatory plans are monitored, progress / variance communicated to the Global Regulatory Lead and SeniorManagement
• Ensures business compliance and implementation of and adherence to Regulatory standards

Your Background

• Hold a relevant scientific degree or have equivalent working experience
• Previous experience as a national and / or regional regulatory liaison for at least one product in different therapeutic areas and in different stages of the product life cycle
• Knowledge of drug development practice rules, regulations and guidelines
• Experience in communicating with FDA or major EU regulatory agency(ies) for US and EU regulatory strategists
• Proven ability in developing and implementing regulatory strategy

Company

Our client is one of the world's premier innovative biopharmaceutical companies, discovering, developing and providing over 160 different medicines, vaccines and consumer healthcare products to help improve the lives of millions of people in the UK and around the world every year.