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6 month contractPAYEHybridExcellent pay rate
Our client is a global medical technology company, who design and manufacture technology that takes the limits off living. They support healthcare professionals to return their patients to health and mobility, helping them to perform at their fullest potential.
Role Overview:
Responsible for providing administrative and operational support to Global Clinical Operations to ensure efficient and effective conduct of clinical studies to industry and company standards while meeting study requirements and targets. This position has administrative responsibilities for Study Site Feasibility, Study Support and Essential Document Management.
Responsibilities:
- This role will provide administrative support as assigned such as, ordering of supplies, filing of documents, study binder/supply and investigational product shipping to ensure achievement of study goals and timelines from study start-up through study close-out. (30%) 
- Assist with data entry and reporting of study information using applicable systems (i.e., CTMS, Sharepoint, eTMf Track and reconcile essential documents for Central Master Files according to ICH GCP and/or ISO 14155 and company procedures; ensure quality of documentation and archiving. (30%) 
- Track and maintain study logistic information, systems and tools. (10%)
- Under the direction of CSM, organize and coordinate the logistics of internal and external meetings such as Advisory Board meetings and investigator meetings. (5%) 
- Under direction of CSM, prepare meeting minutes and other study documentation as reqired. (5%) 
- Other duties, as assigned such as, ordering of supplies, filing of documents, study binder/supply and investigational product shipping. (10%) 
- Work within established SOPs; identify and under direct supervision, suggest process improvements. (10%)
Competences
(1) Ability to handle assigned projects(2) Ability to effectively follow and give written/oral instructions(3) Contribute to positive team environment (4) Professional communication skills with solid oral and written English(5) Attention to detail (6) Knowledge of US Code of Federal Regulations, ISO 14155, ICH GCP
Experience:
Minimum 1-2 years' experience in clinical research industry with strong business administration skills.
