Senior Project Coordinator Clinical

1 day ago

London, Greater London, United Kingdom ARTHEx Biotech Full time
About the Role

The Senior Project Coordinator Clinical will play a key role in the planning and execution of clinical trials within the Clinical Department at ARTHEx Biotech. This individual will be responsible for providing administrative support to ensure smooth project operations, including budget management, contract negotiation, and vendor management.

The ideal candidate will have a strong understanding of clinical operations, including protocol concept, clinical study reporting, and regulatory submissions. A background in the pharmaceutical or biotechnology industry is highly desirable, with a minimum of 5 years of experience in clinical operations.

You will be responsible for overseeing document management processes, ensuring adherence to SOPs and regulatory requirements. Additionally, you will assist in the completion of clinical and regulatory documents, such as Clinical Trial protocols, Investigator Brochures, Clinical Trial Applications, etc.

The successful candidate will have excellent interpersonal, written, and verbal communication skills, as well as proven organizational skills. They will be able to work collaboratively within the company, with the Director, Clinical Project Management, and CROs/vendor partners to plan and execute clinical trials.

This is an exciting opportunity to join a dynamic team and contribute to the development of innovative medicines through the modulation of gene expression. If you are a motivated and experienced professional looking to take your career to the next level, we encourage you to apply.

Responsibilities
  • Provide administrative support to ensure smooth project operations, including budget management, contract negotiation, and vendor management
  • Oversee document management processes, ensuring adherence to SOPs and regulatory requirements
  • Assist in the completion of clinical and regulatory documents, such as Clinical Trial protocols, Investigator Brochures, Clinical Trial Applications, etc.
  • Work collaboratively within the company, with the Director, Clinical Project Management, and CROs/vendor partners to plan and execute clinical trials
Requirements
  • Bachelor's degree in a scientific/life sciences discipline, or equivalent experience
  • Minimum of 5 years of experience in clinical operations
  • Strong understanding of clinical operations, including protocol concept, clinical study reporting, and regulatory submissions
  • Excellent interpersonal, written, and verbal communication skills
  • Proven organizational skills, including ability to prioritize tasks, manage multiple projects, and meet deadlines
Salary Information

The estimated salary for this position is $80,000 - $110,000 per year, depending on experience. Benefits include health insurance, retirement savings plan, and paid time off.

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