Associate Director Clinical Operations
Associate Director Clinical Operations

Associate Director Clinical Operations

London Full-Time 54000 - 84000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead clinical programs and manage cross-functional teams to execute complex trials.
  • Company: Join a globally renowned mid-sized pharmaceutical company focused on rare disease drug development.
  • Benefits: Enjoy competitive salary, career growth opportunities, and a collaborative work environment.
  • Why this job: Make a real impact in the rare disease space while working with industry leaders.
  • Qualifications: BA/BSc/PhD in life sciences and 10 years of experience in biotech or pharmaceuticals required.
  • Other info: Reach out to jamie.stephens@arto-talent.com for more information.

The predicted salary is between 54000 - 84000 £ per year.

ARTO is currently partnered with a globally renowned mid-sized Pharmaceutical company who are committed to the development of drugs within the Rare Disease space. Within their Global Clinical Operations team, they are looking for an Associate Director who will be able to lead Clinical programs and projects as well as manage a cross-functional group to execute complex trials.

Key Responsibilities:

  • Contribute to clinical strategies for programs, providing leadership on the design and execution of CDPs.
  • Provide guidance on all relevant program and study deliverables.
  • Provide program-level oversight, leadership, and direction ensuring Operations team members achieve deliverables within timelines, budgets and in accordance with GCP and company standards.
  • Give strategic guidance and reports on program progress, risks, issues and metrics as needed to executive leadership.
  • Drive cross-functional initiatives across the portfolio of programs.

Qualifications:

  • BA/BSc/PhD with a focus on life sciences.
  • 10 years experience within biotech and pharmaceutical companies leading clinical trial or drug development initiatives.
  • Team management experience.

If this role could be something of interest to you, please feel free to apply through the job advertisement or reach out to me at jamie.stephens@arto-talent.com.

Associate Director Clinical Operations employer: ARTO

ARTO is an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration within the Rare Disease sector. Employees benefit from comprehensive professional development opportunities, competitive remuneration, and a supportive environment that values their contributions. Located in a vibrant area, the company promotes a healthy work-life balance, making it an ideal place for those seeking meaningful and rewarding careers in clinical operations.
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Contact Detail:

ARTO Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Associate Director Clinical Operations

✨Tip Number 1

Network with professionals in the pharmaceutical and biotech industries. Attend industry conferences or webinars where you can meet people who work in clinical operations. This can help you gain insights into the role and potentially get referrals.

✨Tip Number 2

Familiarise yourself with the latest trends and regulations in clinical operations, especially related to rare diseases. Being knowledgeable about current challenges and innovations can set you apart during discussions with hiring managers.

✨Tip Number 3

Prepare to discuss your leadership style and experiences in managing cross-functional teams. Be ready to provide specific examples of how you've successfully led clinical trials or projects, as this will demonstrate your capability for the Associate Director role.

✨Tip Number 4

Research the company’s pipeline and recent developments in their drug portfolio. Showing that you understand their mission and how you can contribute to their goals will make a strong impression during any interviews.

We think you need these skills to ace Associate Director Clinical Operations

Leadership Skills
Clinical Trial Management
Project Management
Cross-Functional Team Coordination
Regulatory Knowledge (GCP)
Strategic Planning
Risk Management
Budget Management
Communication Skills
Problem-Solving Skills
Data Analysis
Stakeholder Engagement
Time Management
Adaptability
Mentoring and Coaching

Some tips for your application 🫡

Tailor Your CV: Make sure your CV highlights relevant experience in clinical operations, particularly in leading clinical trials and drug development initiatives. Use specific examples that demonstrate your leadership skills and ability to manage cross-functional teams.

Craft a Compelling Cover Letter: Write a cover letter that clearly outlines your passion for the pharmaceutical industry and your experience with rare diseases. Address how your background aligns with the key responsibilities of the Associate Director role and how you can contribute to the company's goals.

Highlight Relevant Qualifications: In your application, emphasise your educational background in life sciences and any advanced degrees. Mention your 10 years of experience in biotech or pharmaceutical companies, focusing on specific projects or programs you've led.

Showcase Leadership Experience: Detail your team management experience in your application. Provide examples of how you've successfully guided teams through complex trials, ensuring deliverables are met within timelines and budgets, while adhering to GCP and company standards.

How to prepare for a job interview at ARTO

✨Showcase Your Leadership Skills

As an Associate Director, you'll need to demonstrate your ability to lead teams effectively. Prepare examples from your past experiences where you successfully managed cross-functional groups and drove projects to completion.

✨Understand the Rare Disease Landscape

Familiarise yourself with the current trends and challenges in the rare disease space. Being knowledgeable about the specific therapeutic areas relevant to the company will show your genuine interest and commitment to the role.

✨Prepare for Strategic Discussions

Expect questions around clinical strategies and program oversight. Be ready to discuss how you would approach designing and executing clinical development plans, as well as how you would manage risks and issues that may arise.

✨Highlight Your Compliance Knowledge

Since the role requires adherence to GCP and company standards, be prepared to discuss your experience with regulatory compliance in clinical trials. This will reassure the interviewers of your capability to maintain high standards in operations.

Associate Director Clinical Operations
ARTO
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  • Associate Director Clinical Operations

    London
    Full-Time
    54000 - 84000 £ / year (est.)

    Application deadline: 2027-06-17

  • A

    ARTO

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