Clinical Research Associate 2

4 days left

Company
Northreach
Location
Remote
Salary
Up to £40,000 per annum + Allowances
Posted
21 Dec 2020
Closes
20 Jan 2021
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)

Northreach is currently partnering with a rapidly growing CRO based in Welwyn garden city who are currently on the hunt for a CRA 2 to join their team on a permanent basis. This role is a home-based role with occasional trips to the office when necessary.

General Day to day responsibilities

  • Manage workload priorities ensuring the more urgent and important tasks are completed first within required timescales
  • Planning and Delivery
  • Site Management/Monitoring to Closeout, Site initiation/training, Site set-up, Site selection
  • Complete timesheets for each project assigned.  
  • Work with the Head of Clinical Operations and Senior Clinical Study/Project Manager and support process improvements related to the role and/or cross-functional teams, including generation of controlled forms, SOPs, and Guidance Documents 
  • Encourage a team culture that fits within the companies work ethos creating a team environment that supports process improvement, innovation, and personal accountability
  • Undertake travel as required to fulfil post (this may involve international travel)
  • Undertake any other duties commensurate with the position

Knowledge and skills

Essentials

  • Demonstrated experience (2-3years+) of monitoring multiple, multicentre Interventional clinical trials at a CRA-I level (or equivalent)
  • Previous experience in undertaking ethics and/or regulatory submissions
  • Strong organisational and time management skills
  • Excellent interpersonal skills both written and verbal. Ability to confidently communicate with an array of internal and external contacts.
  • Scrupulous attention to detail and ability to meet deadlines
  • Ability to work as part of a team and independently in an enthusiastic, pro-active fashion 
  • Willingness to travel as required for monitoring projects assigned (may include international travel)
  • Educated to degree level or equivalent (preferably in a science related subject) 
  • Experience of collecting, handling, and tracking data
  • Extensive knowledge of Microsoft based packages and database applications such as Access and Excel
  • Detailed knowledge of ICH/GCP guidelines, EU Clinical Trials Directives (as amended) and FDA regulations and guidelines (as amended)

Desirables

  • Early phase/oncology experience  
  • Familiarity with ISO 14155 and the Medical Devices Directive

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