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Clinical Trials Associate


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https://www.pop-science.co.uk/1736-clinical-trials-associate/clinical-research/central-london/job2024-02-12 11:01:281970-01-01 Pop Science
Job Type Permanent Full Time
Location London
Area Central London, UK Central London UK London
Sector Clinical Research
Salary £20k - 35k per year
Currency gbp
Start Date ASAP
Advertiser remoteapi
Job Ref 1413
Job Views 294
Description

We have a great role, working at our client, an exciting CRO in London as a CTA. Their Clinical Trials Assistant is a key member of the project team and will provide in-house operational support to study teams, ensuring standardisation and consistency of tracking across studies in accordance with SOPs.

This is a great role for learning more about clinical trials, study site management and working with data platforms. 

Key Responsibilities:

  • Day to day operational support to Lead Ops, CPMs, CRAs for defined tasks during study
  • Collects, co-ordinates and maintains essential documents and the Trial Master File (TMF)
  • Logistics of investigator and monitor meetings organised including the development of presentation materials under direction of PM
  • Support study team meetings including preparation of agendas and minutes, action logs and Q&A documents as needed
  • Documents learnings and recommendations from study debriefs and best practice identified and implemented in collaboration with manager and colleagues
  • Assists in the preparation, review, finalisation and distribution of study Newsletters for investigators and monitors
  • Study area managed according to standards including set up, access rights and maintenance of study related documents
  • Development and maintenance of study specific documents, tracking tools and systems and reports study metrics to team under direction of PM
  • General filing and ad hoc administrative tasks
  • Documentation provided to support the preparation of clinical study reports and publications
  • Health Authority/ IRB submissions and approvals tracked
  • Maintain all documentation in a complete and accurate manner
  • Awareness of and compliance to laws and regulations applicable to projects
  • Awareness of and compliance to all policies and procedures including: Finance, Procurement, IT and Legal
  • Attending all requisite training sessions and completion of all requisite on-line training and compliance programmes within specified time limit
  • Additional responsibilities as directed, within the scope of the role
  • Candidates will need to have current and valid eligibility to work in the UK in order to be considered for this role.

 

Desired skills and experience

  • Good Accuracy and Attention to detail
  • Excellent written and verbal communication skills
  • Excellent IT literacy
  • Team player
  • Excellent planning and organising skills
  • Understanding of regulations and SOPs
  • Able to manage smaller projects/tasks

Contact Gail Kniveton for more information

#clinicaltrialassociate #cta #pharmajobs #clinicaltrialsassistant

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