Naukrijobs UK
Register
London Jobs
Manchester Jobs
Liverpool Jobs
Nottingham Jobs
Birmingham Jobs
Cambridge Jobs
Glasgow Jobs
Bristol Jobs
Wales Jobs
Oil & Gas Jobs
Banking Jobs
Construction Jobs
Top Management Jobs
IT - Software Jobs
Medical Healthcare Jobs
Purchase / Logistics Jobs
Sales
Ajax Jobs
Designing Jobs
ASP .NET Jobs
Java Jobs
MySQL Jobs
Sap hr Jobs
Software Testing Jobs
Html Jobs
IT Jobs
Logistics Jobs
Customer Service Jobs
Airport Jobs
Banking Jobs
Driver Jobs
Part Time Jobs
Civil Engineering Jobs
Accountant Jobs
Safety Officer Jobs
Nursing Jobs
Civil Engineering Jobs
Hospitality Jobs
Part Time Jobs
Security Jobs
Finance Jobs
Marketing Jobs
Shipping Jobs
Real Estate Jobs
Telecom Jobs

Clinical Research Associate

Randstad Sourceright
Job LocationHull
EducationNot Mentioned
Salary£25.00 - £30.00 per hour
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypeContract , full-time Work from home12

Job Description

Smith + Nephew is a global medical technology company. We design and manufacture technology that takes the limits off living. We support healthcare professionals to return their patients to health and mobility, helping them to perform attheir fullest potential.From our first employee and founder, T.J. Smith, to our team today, it’s our people who make Smith+Nephew a unique place.Yes, we love to innovate and develop exciting technologies, and we offer competitive salaries and progressive benefits. But it’s our culture - of Care, Collaboration and Courage - that really sets us apart.Through a spirit of ownership and can-do attitude, we work together to win.We’re a company of people who care about each other, about our customers and their patients, and about our communities.Role OverviewResponsible 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 hasadministrative responsibilities for Study Site Feasibility, Study Support and Essential Document ManagementEssential Functions

  • 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 ICHGCP and/or ISO 14155 and company procedures; ensure qualityof 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 required. (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%)
Required ExperienceMinimum 1-2 years experience in clinical research industry with strong business administration skills.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, ICHGCP(7) Knowledge of Essential Documents.

APPLY NOW

Clinical Research Associate Related Jobs

© 2019 Naukrijobs All Rights Reserved