Biotechnology Project Lead

1 day ago


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

ARTHEx Biotech is a clinical-stage biotechnology company focused on developing innovative medicines through the modulation of gene expression. Our lead investigational compound, ATX-01, is being evaluated for the treatment of myotonic dystrophy type 1 (DM1), a rare neuromuscular disorder, in the Phase I-IIa ArthemiRTM trial.

We are committed to advancing the development of novel treatments for disorders with high unmet medical needs, including genetically-driven diseases like DM1. Our team is dedicated to delivering high-quality results while upholding the highest standards of ethics and integrity.

If you are a talented professional looking to join a dynamic team and contribute to the development of innovative medicines, we encourage you to apply for the Biotechnology Project Lead position.

Job Summary

We are seeking a highly motivated and experienced Biotechnology Project Lead to join our team at ARTHEx Biotech. The successful candidate will be responsible for leading the planning and execution of clinical trials within the Clinical Department.

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 10 years of experience in clinical operations.

You will be responsible for overseeing site selection, activation, and monitoring activities, ensuring compliance with study protocols, regulatory requirements, and relevant SOPs. Additionally, you will provide direction for the study team, ensuring alignment with organizational goals and objectives.

Responsibilities
  • Lead the planning and execution of clinical trials within the Clinical Department
  • Oversee site selection, activation, and monitoring activities, ensuring compliance with study protocols, regulatory requirements, and relevant SOPs
  • Provide direction for the study team, ensuring alignment with organizational goals and objectives
  • Collaborate 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 10 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 leadership qualities, including ability to train others, decision-making, problem-solving, negotiating, etc.
Salary Information

The estimated salary for this position is $140,000 - $180,000 per year, depending on experience. Benefits include health insurance, retirement savings plan, and paid time off.



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