Senior Clinical Research Coordinator

hace 24 horas


Madrid, Madrid, España Tfs Healthscience A tiempo completo

**Job Title:** Senior Clinical Research Coordinator

Are you passionate about driving clinical research initiatives? Do you have a strong understanding of Good Clinical Practice (GCP) regulations and ICH guidelines?

Overview: Tfs Healthscience, a leading global Contract Research Organization (CRO), is seeking an experienced Senior Clinical Research Coordinator to join our Strategic Resourcing Solutions team.

About the Role: As a Senior Clinical Research Coordinator, you will be responsible for ensuring the smooth execution of clinical trials across various sites. Your primary objective will be to monitor site activities, ensure compliance with regulatory requirements, and facilitate effective communication between sites and stakeholders.

Main Responsibilities:

  • Conduct on-site and remote monitoring of clinical trials in accordance with Tfs Healthscience Standard Operating Procedures, FDA regulations, and GCP/ICH guidelines.
  • Review CRFs (paper or electronic) and subject source documentation for validity and accuracy, generating queries as needed to resolve discrepancies.
  • Identify site problems/deficiencies and escalate them to management through trip reports, memos, and verbal updates.
  • Foster collaboration with Project Managers and Lead CRAs to implement corrective actions and resolve issues efficiently.

What We Offer: Competitive compensation package ($60,000 - $80,000 per annum), comprehensive benefits, and opportunities for professional growth in a dynamic environment. Join our team and contribute to delivering high-quality clinical research services worldwide.

Requirements:

  • Bachelor's Degree in Life Sciences or Nursing; equivalent experience accepted.
  • Minimum 2-3 years of relevant clinical research experience, preferably in a CRO setting.
  • Proven ability to work in fast-paced environments with changing priorities.
  • Strong understanding of medical terminology, basic science associated with assigned drugs, and therapeutic areas.
  • Familiarity with GCP, ICH, and regulatory requirements.


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