Assumes responsibility for an individual project, or many projects
Communicates in an optimal way, making sure that specific client objectives are met
Responsible for the set-up and maintenance of the project(s)
Partially responsible for the development of research protocols and documents, such as CRF, publications and clinical reports
Responsible for the management of the study budget
Establish and manage the study time-lines and protocol specific SOPs
Ensuring that the many different tasks during clinical development and marketing are achieved
Selection of research sites
Involves little to no people management and focuses completely on the product development programme and trials
Qualifications
Experience within the clinical trial management field, with some experience of taking a lead CRA role in the management of studies/trials. Five years experience within the clinical monitoring arena is preferred.
Thorough knowledge of ICH GCP and relevant regulations for the conduct of clinical trials.
Knowledge of project management processes and tools.
Fluent in written and spoken English. Additional language skills desirable.
Computer literate.
Due to the nature of this position it may be required for the employee to travel.
University/Bachelors Degree in medicine, science or equivalent degree/experience.
