eTMF Specialist, Clinical Operations, Study Coorindator, Data Manager, Site Manager
A long-term 12-month contract has become available for an experienced clinical operations manager with a strong understanding of clinical trials and document management. You will be working at one of the world’s top independent Biotechnology companies, based at their Greater London site, given a host of responsibility for supporting leaders for department strategies.
This position is a great opportunity for a clinical operations professional with a strong background in study management as well as direct management experience:
Motivate and develop teams: encouraging best practices.
Primary records management contact for regulatory authorities.
Responsible for developing strong relationships, including internal and external.
Global stakeholder management.
Clinical document management
This established Pharmaceutical/Biotech company has seen groundbreaking success in its clinical research, producing some of the most innovative medicines onto market. Their products range from Inflammation to Oncology and their success over the last 15 years has resulted in the growth of the company, now home to hundreds of employees globally they are recognised as a world leader in the development of medicines.
This position would be suitable for an experienced consultant with a strong understanding of drug safety requirements.
Either a doctorate degree and 4 years industry experience; OR master’s degree and 8 years industry experience.
Good knowledge of global regulatory requirements and standard operating procedures.
Project management experience.
Change management experience.
Strong understanding of ICH-GCP.
Must have strong understanding of clinical trials and study management experience.
Contract Length – 12-months.
Location – UK
They are looking to shortlist candidates in the next coming days and so do not hesitate to apply.
Please contact Keeley Munday on 02030196022 or email your CV to firstname.lastname@example.org