Location: London, United Kingdom.
Contract: Full Time
Salary: Competitive (Dependent on experience)
Monitoring of clinical trial sites and ensuring that the conduct of the trial follows
applicable regulatory requirements and GCP.
Communicate with other scientists in identifying and resolving technical issues with
specimen or documentation.
Provide support for the development of all trial-related documents.
Participating in the design and implementation of clinical trials, including writing protocols
and collecting data.
BSc in any relevant scientific field.
At least three years prior research experience in the life sciences industry.
Clinical research and project management skills.
Experience with the development of clinical trial protocols.
Budget and time management skills.
Leadership and good interpersonal skills.
I am looking forward to having a chat with you if you are suitable for this role. For more
information on this exciting opportunity please email a copy of your CV in MS WORD format to
email@example.com using Clinical Research Scientist as Subject.
To stay up to date with latest and exciting opportunities, please follow us on LinkedIn via