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Clinical Operations Leader (LSAD) - Oncology Experience Required - UK - FSP

Parexel

Uxbridge

Remote

GBP 50,000 - 90,000

Full time

9 days ago

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Job summary

An established industry player is seeking a Clinical Operations Leader to manage local clinical trials in oncology. This role offers the opportunity to work remotely while collaborating with top biotechs and pharma companies. You will lead a dedicated team, ensuring the successful delivery of clinical studies while adhering to regulatory standards. With a commitment to professional growth, this position provides a supportive environment where your skills can flourish. If you are passionate about clinical research and looking for a role that balances professional challenges with personal life, this opportunity is for you.

Qualifications

  • 3+ years managing local clinical trials with a focus on oncology.
  • Strong leadership and organizational skills to deliver high-quality trials.

Responsibilities

  • Manage clinical study components according to budget and timelines.
  • Ensure compliance with regulations and timely submissions to authorities.

Skills

Leadership Skills
Clinical Trial Management
Oncology Knowledge
Regulatory Submissions
Organizational Skills
Interpersonal Skills
Problem-Solving Skills

Education

Bachelor's Degree in Life Sciences

Job description

Clinical Operations Leader (LSAD) - Oncology Experience Required - UK - FSP

Parexel Uxbridge, England, United Kingdom

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Clinical Operations Leader (LSAD) - Oncology Experience Required - UK - FSP

Parexel Uxbridge, England, United Kingdom

2 days ago Be among the first 25 applicants

Join to apply for the Clinical Operations Leader (LSAD) - Oncology Experience Required - UK - FSP role at Parexel

Parexel is currently seeking a Local Study Associate Director (Clinical Operations Leader) to join us in the UK. You will be assigned to one of our key sponsors in the region.

Working as a Local Study Associate Director (LSAD) at Parexel FSP offers long-term job security and growth opportunities. We undertake vital clinical studies for sponsors including leading global biotechs and Pharma top 50, with an impressive pipeline of work.

Whether your future path is in clinical operations, project management, line management, or other roles, we offer a world of opportunities.

Our LSADs work remotely from their home office, supporting studies within their country or region. Our mantra is ‘Manageable sites, manageable protocols’. Expect professional challenges in inspiring studies, balanced with time for your personal life.

Role specifics:
  • Dedicated to one client.
  • Responsible at the country level for delivering clinical study components according to resources, budget, timelines, and compliance with Client Procedural Documents, ICH-GCP, and local regulations.
  • Ensures timely preparation of country financial Study Management Agreement (fSMA) and maintains accurate study budgets in the financial system.
  • Leads and optimizes the performance of the Local Study Team(s), ensuring compliance with procedures and regulations.
  • Prepares country-level Master Informed Consent Forms (MICF) and site-level ICFs, including translations, in line with SOPs and regulations.
  • Ensures timely submission of applications/documents to EC/IRB at study start-up and throughout the study.
Requirements:
  • Minimum of 3 years' experience managing local clinical trials.
  • Proven leadership and motivation skills to deliver trials on time, within budget, and with quality.
  • Willingness and ability to monitor oncology trials as needed.
  • Experience with submissions to Regulatory Authorities and Ethics Committees.
  • Ability to collaborate with study functions for smooth delivery.
  • Strong organizational, interpersonal, and problem-solving skills; ability to multitask and prioritize.
  • Good understanding of clinical research phases, GCP/ICH guidelines, and local laws.

We value our people and foster an open, friendly environment that empowers growth and development within Parexel.

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