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Head of Clinical Operations

ARTO

Greater London

On-site

GBP 80,000 - 120,000

Full time

10 days ago

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Job summary

An innovative biotechnology company is seeking a dynamic Head of Clinical Operations to lead Phase I clinical trials in ophthalmic diseases. This pivotal role involves overseeing the planning, execution, and delivery of clinical trials, ensuring compliance with regulatory standards, and building a high-performing team. The ideal candidate will have over a decade of experience in clinical operations, with a strong track record in leadership and project management. Join a forward-thinking organization at the forefront of gene therapy and make a significant impact in the biotech field.

Qualifications

  • 10+ years of clinical operations experience in biotech or pharma.
  • Proven track record of leading Phase I and II clinical trials.
  • Strong understanding of ICH-GCP and FDA regulations.

Responsibilities

  • Oversee planning and execution of clinical trials.
  • Lead development of clinical operations strategy.
  • Ensure trials comply with regulatory requirements.

Skills

Clinical Operations Management
Project Management
Leadership Skills
Regulatory Compliance
Communication Skills

Education

Bachelor's Degree in Life Sciences
Master's Degree in a related field

Job description

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Helping biotech and pharma companies place Medical Director-Vice President level candidates in clinical development in the fields of Immunology…

ARTO is currently partnered with a early stage, European biotechnology company specialising in Ophthalmic diseases using innovative Gene Therapies. With upcoming Phase I clinical trials, they are searching for an experienced Clinical Operations leader to drive these first in human studies.

As Head of Clinical Operations, you’ll be responsible for overseeing the planning, execution, and delivery of our clinical trials. You’ll work closely with cross-functional teams and senior leadership to ensure our programs are designed and run efficiently and also meet regulatory requirements. This is a key leadership role.

Key Responsibilities

  • Lead the development and execution of clinical operations strategy across all programs.
  • Oversee all aspects of clinical trial management, including site selection, vendor oversight, patient recruitment, monitoring, and study close-out.
  • Build and manage a high-performing Clinical Operations team
  • Partner with Clinical Development, Regulatory and Quality to ensure alignment on trial design and execution
  • Ensure trials are conducted in compliance with GCP, regulatory requirements, and company SOPs.
  • Cultivate strong relationships with investigators, CROs, and other external partners.
  • Serve as a key point of contact during regulatory inspections and audits.

Qualifications

  • 10+ years of clinical operations experience in biotech or pharma, with at least 5 years in a leadership role.
  • Proven track record of successfully leading Phase I and II clinical trials.
  • Deep understanding of ICH-GCP, FDA regulations, and international clinical research guidelines.
  • Strong leadership skills with the ability to build, mentor, and inspire a growing team.
  • Excellent project management, organizational, and communication skills.
  • Comfortable operating in a fast-paced, dynamic environment with evolving priorities.
Seniority level
  • Seniority level
    Director
Employment type
  • Employment type
    Full-time
Job function
  • Job function
    Project Management
  • Industries
    Pharmaceutical Manufacturing and Biotechnology Research

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