CK Group are recruiting for a Regulatory Project Lead to join a company in the healthcare industry at their site based in Brentford on a contract basis for either 6 or 12 months. Hourly £34.82 Regulatory Project Lead Role: Accountable to GRL/ Regional Rep/ C&EP lead for delivery of submissions or strategy components for an assigned product in development or marketed product; planning own and submission team activities to ensure delivery to agreed timeframes and appropriate content Responsible for the implementation of the submission strategy for TG supported markets Responsible for the development and implementation of the submission strategy for NCE Global Delivery supported markets Ensures quality of both own and submission team work and compliance with regulatory guidelines and process as they apply to the role. Your Background: Biological or healthcare science qualification or extensive experience within Regulatory Affairs in the Drug development environment Broad understanding of the pharmaceutical industry, drug development environment, and R&D processes and objectives. Global/ EMAP Regulatory submission experience - Knowledge of regulatory agency guidelines and expectations for submissions. Excellent organisational skills, attention to detail and commitment to deliver high quality output, even under pressures sometimes demanded by regulatory deadlines and managing multiple submissions simultaneously Company:Our client is a global healthcare company, taking on some of the world's biggest healthcare challenges. Location: This Regulatory Project Lead role will be based at our clients site in Brentford, Greater London. Apply: For more information, please contact Lucy Stendall on 01246 457725 or email [email protected] Please quote reference 48460. It is essential that applicants hold entitlement to work in the UK We'll store this in session so if you're applying for multiple jobs today so you can use this as a base.