Clinical Trials Manager

4 weeks ago

Swansea, United Kingdom Smart Solutions Recruitment Full time €45,000

SmartPro are working with an award winning manufacturer based in Swansea. We are seeking for an enthusiastic experienced Clinical Trials Manager to join our Clinical and Application Research department. You will be responsible for all aspects of clinical trial management. The post holder will have a significant level of responsibility. Duties will include designing plus authoring trial documentation and regulatory submissions, plus monitoring the progress and performance of multiple trials from participant identification and recruitment through to ensuring reliable data collection. Key Responsibilities of the Clinical Trials Manager:

  • Design clinical and application research studies.
  • Author Clinical Investigation Plans (CIP) and Final Study Reports (FSR)
  • Statistically analyse clinical data
  • Draft clinical manuscripts for publication
  • Prepare abstracts, power-point presentations and posters for submission to scientific conferences.
  • Understand how clinical data can best assist product launch/sales.
  • Conduct audits and trend /gap analysis on key elements of trial execution.
  • Assume PI responsibility for all clinical trials.
  • Maintain up-to-date knowledge of relevant industry guidelines.
  • Oversee activity of trial sites
  • Contribute to all trial management activities including budgeting.
  • Develop operational project plans.
  • Manage trial associates, investigators, and other trial personnel to ensure personnel are up to date with relevant information or issues. Delegate workloads accordingly
Requirements of the Clinical Trials Manager:
  • BSc or equivalent in biomedical, health of life science field.
  • Proven clinical trial experience, clinical trial management; CRO experience preferred.
  • Experience in Phase I-IV trials; Phase II - III is preferred.
  • Working knowledge of EU Clinical Trials Directive, Medical Device Directive, UK Clinical Trials Regulations, Principles of ICH-GCP, GDPR and Research Governance Framework Legislation with proven ability to apply these to the coordination of clinical trials.
  • Understanding of current EU Medical Device Regulation.
  • Evidence of preparing regulatory and ethics submissions, writing/amending Clinical Investigation Plans, Patient Information Forms and electronic Case Report Forms, plus other relevant trial management documentation.
  • Working knowledge of BS EN ISO 14155.
  • Strong, professional leadership experience.
What you will get:
  • Attractive starting salary between £45,000
  • Permanent Contract with career progression
  • Excellent company package including workplace pension, life assurance, product discounts and healthcare plan.
If this sounds of interest to you and you would like to find out more then why not click apply today and one of our team will come back to you

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