Find Your Perfect Job

Regulatory Writer - Cambridgeshire - Consultancy

Regulatory Writer - Cambridgeshire - Consultancy A fantastic opportunity has arisen for an experienced Regulatory Writer to join a leading global consultancy in Cambridgeshire in the South East of England.

Senior Regulatory Affairs Associate LPO

Senior Regulatory Affairs Associate LPO - Pharmaceutical Experienced Regulatory Affairs professional wanted to join a global Pharmaceutical company as a Senior Regulatory Affairs Associate LPO, the role will be based in Warwickshire in the West Midlands but offers up to 3 days per week home working.

Regulatory Affairs Associate RPO - Pharmaceutical

Regulatory Affairs Associate RPO - Pharmaceutical An amazing opportunity has arisen for an experienced Regulatory Affairs professional to be part of a global Pharmaceutical company as a Regulatory Affairs Associate within the RPO team, the role offers partial home working but will also be based in Warwickshire in the West Midlands.

Regulatory Writer - North West - Consultancy

Regulatory Writer - North West - Consultancy Experienced Regulatory Writer wanted to join a very successful medical communications consultancy based in Cheshire in the North West of England.

Qualified Person/Quality Assurance Manager - Kent

Quality Assurance Officer - Contract

Optical Physicist/Engineer - Taunton

Optical Physicist/Engineer - Taunton There is currently an urgent requirement for an experienced Optical Engineer to work on a range of cutting-edge projects with one of the largest manufacturers of precision optical products in the world. You will be joining a new team of experts in the design, development and delivery of brand new projects and services to the optical sector.

Senior Medical Advisor

Senior Medical Advisor- Surrey- South East- Pharmaceuticals An excellent opportunity has arisen for a Senior Medical Advisor to join a Global and highly reputable Pharmaceutical company at one of their sites based in Surrey, Southeast. The company is one of the world’s most successful pharmaceutical companies and they have operational sites in over 130 countries. The company prides themselves on their ability to develop new and innovative medicines with the aim to help to prevent and cure diseases and to improve the quality of life.

Clinical Trial Monitor

Key Responsibilities: The successful Clinical Trial Assitant (CTA) will be responsible for performing study site management activities. This includes Start up activities, regulatory compliance, patient enrolment, CRF compliance and data quality for Clinical Trials as well as developing and maintaining investigator relationships.

Statistical Programmer – Midlands