Clinical Research Coordinator

1 month ago


Reading, Reading, United Kingdom Lifelancer Full time

We are seeking a skilled and detail-oriented Trial Support Specialist to join our team at Lifelancer, a leading talent-hiring platform in Life Sciences, Pharma, and IT.

**Job Summary:**

The ideal candidate will have minimum 6 months of clinical research experience and possess strong organizational skills, effective time management, and excellent communication abilities. This role is responsible for performing daily administrative activities, collaborating with clinical teams, and ensuring accurate trial master file delivery.

**Key Responsibilities:**

  • Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up teams with updating and maintaining clinical documents and systems.
  • Collaborate with the clinical team on preparation, handling, distribution, filing, and archiving of clinical documentation and reports.
  • Review study files and completeness periodically.
  • Coordinate tracking and management of Case Report Forms (CRFs), queries, and clinical data flow.

**Required Skills and Qualifications:

  • Knowledge of applicable clinical research regulatory requirements (GCP and ICH).
  • Minimum 6 months of clinical research experience.
  • Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint).
  • Effective written and verbal communication skills.
  • Time management and organizational skills.
  • Ability to establish and maintain effective working relationships.

**Benefits:

  • A competitive salary between £25,000 - £35,000 per annum.
  • Ongoing training and development opportunities.
  • Hybrid working arrangement with 2-3 days on-site in Luton.

**About Us:**

Lifelancer is a talent-hiring platform connecting professionals with opportunities in pharma, biotech, health sciences, healthtech, data science, and IT domains. If you are passionate about clinical research and want to be part of a dynamic team, please apply through the provided link.

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