Clinical Operations Lead

Proclinical Staffing; London; On-site; GBP 70,000 - 90,000; Full time

Job summary

A prominent pharmaceutical company in London is seeking a Clinical Operations Lead to manage clinical trials in oncology. The role involves leading operational teams, establishing relationships with vendors, and ensuring adherence to clinical regulations. Candidates should possess strong leadership skills, knowledge of drug development, and a relevant degree. This opportunity offers the chance to make a significant impact in pharmaceutical innovation.

Qualifications

• Proven ability to lead teams in clinical studies from start to finish.
• Experience with ICH-GCP guidelines and clinical operations.
• Adaptability and agility in ambiguous environments.

Responsibilities

• Develop and manage operational plans and budgets for clinical studies.
• Oversee vendor and stakeholder relationships.
• Implement risk mitigation strategies adhering to regulations.
• Manage clinical resources and forecasts.
• Lead feasibility assessments for trial participation.

Skills

Strong leadership skills

Knowledge of drug development process

Experience in clinical trial management

Ability to thrive in fast-paced environments

Education

University degree in life sciences or equivalent

Job description

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Ready to lead projects that bring life-changing treatments to the world? Join our client at the forefront of pharmaceutical innovation and make a difference!

Proclinical is seeking a Clinical Operations Lead to support the delivery of clinical trials in oncology. In this role, you will lead or contribute to cross-functional global teams, ensuring operational excellence across all phases of clinical studies. This position focuses on driving innovation in clinical trial delivery, with the patient at the center of all activities.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Develop and manage operational plans, including clinical study budgets, to ensure consistency and efficiency.

• Oversee vendor and stakeholder relationships, ensuring performance and alignment with project goals.
• Establish yourself as a leader within the team, inspiring others and sharing best practices.
• Manage risk and compliance by implementing site monitoring and risk mitigation strategies, adhering to ICH-GCP and other regulations.
• Oversee resource management, including forecasting and maintaining supplies for clinical studies.
• Lead feasibility assessments to select appropriate countries and sites for trial participation.
• Provide guidance to country operational representatives and maintain strong external stakeholder relationships.

• Contribute to clinical operations communities, enabling innovative trial delivery and addressing emergent needs.

Key Skills and Requirements:

• Strong leadership skills with the ability to guide teams in executing clinical studies from start to finish.
• Working knowledge of the drug development process and regulations, including ICH-GCP guidelines.
• Experience in clinical trial management, with a focus on operational efficiency and stakeholder collaboration.
• Ability to thrive in fast-paced, collaborative environments and adapt to ambiguity.
• A university degree or equivalent experience, preferably in life sciences.

If you are having difficulty in applying or if you have any questions, please contact Joshua Bye at [e-mail].

Apply Now:

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Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

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