Business Type:Pharma
Job Type:Clinical Trial Associate (CTA/SCTA)
Job Level: Experienced
Position: Contract
Location: UK
Reference:CTA/ACT/2014

Closing Date: 25/07/14

Background:

Advanced Clinical Trials (ACT) are recruiting for a permanent CRA to work for a global Sponsor, office based in the UK The Clinical Trial Associate will be working with our clients, the role is through our FSP model.

JOB TITLE
CTA/SCTA

LOCATION
United Kingdom

ROLE/DESCRIPTION

  • Communicates project status to the project team as appropriate.
  • Assists in the retrieval and resolution of issues with transmittals.
  • Scans and copies project documentation inclusive of, but not limited to, essential documents, CSAs, CRFs, and DCFs.
  • Copies, collates and produces study binders.
  • Reviews deliverable to ensure accuracy of content and materials copied.
  • Supports the project team in preparation of documentation for Regulatory and Ethical Submissions.
  • Organizes study documents and materials in compliance with Project and/or Sponsor SOPs regarding regulatory documentation as appropriate.
  • Archives study documentation and returns Trial Master File (TMF) to sponsor, as directed.
  • Reports all document collection and tracking issues to Site Management Services (SMS) Team Lead and/or project team on a regular basis
  • Establishes and maintains QC of the Trial Master File in accordance with project, organizational and regulatory requirements.
  • Files according to client SOPs and/or Sponsor requirements along with clientquality standards and adhere to 98% accuracy across the major files sections and the documents contained therein.
  • Forwards correspondence to sites, sponsors and project teams as needed.
  • Procures, stores, and ships study supplies.
  • Interfaces with vendors as required for a project
  • Participates in internal and external team meetings, taking minutes and providing status updates as required.
  • Provides support to the team communicating process improvement suggestions as applicable.
  • Maintains project server and portal where applicable
  • Proactively identifies, manages, escalates (as needed) and resolves site issues effectively and independently
  • Provides support to Project Team and assume additional roles on the team as necessary

REQUIREMENTS

  • College graduate, preferably with a healthcare or life science degree
  • Secondary school (GCSE) completion

ABOUT ACT CONSULTING
ACT consulting is a part of Advanced clinical Trials a fast growing CRO servicing the Pharmaceutical industry in the UK and Europe. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs).  ACT has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.
www.advancedclinicaltrials.com

Apply Now!

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