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Associate Director, Clinical Trial Delivery (Temporary Contract)

Compass Pathways is a biotechnology company focused on mental health innovations. We are seeking an Associate Director for Clinical Operations to lead clinical trials and ensure quality and compliance.

Skills

  • Project management
  • Organizational skills
  • Communication
  • Interpersonal skills
  • Understanding of clinical trial regulations

Responsibilities

  • Oversee operational execution of clinical trials
  • Manage relationships with clinical trial sites and vendors
  • Develop trial-specific documentation
  • Monitor trial progress and resolve issues
  • Line manage clinical operations professionals
  • Contribute to process improvement
  • Ensure compliance with regulations

Education

  • Bachelor’s degree in life sciences

Benefits

  • Discretionary bonuses
  • Equity
  • Comprehensive benefits package
To read the complete job description, please click on the ‘Apply’ button

Average salary estimate

$200000 / YEARLY (est.)
min
max
$160000K
$240000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Associate Director, Clinical Trial Delivery (Temporary Contract) , Compass Pathways

At Compass Pathways, we're on a mission to reinvent mental health treatments, and we're looking for an Associate Director, Clinical Trial Delivery to join our innovative team. This temporary contract role is essential to the successful execution of our groundbreaking clinical trials, particularly as we advance our unique psilocybin formulation for conditions like treatment-resistant depression. Working closely with cross-functional teams, you'll manage clinical trial operations, ensuring everything runs smoothly while adhering to the highest standards of quality and compliance. You’ll oversee trial management—from maintaining documents and budgets to managing relationships with sites and vendors. Plus, you’ll lead a small team of passionate professionals, providing them with the mentorship and guidance they need to thrive in a collaborative environment. If you have extensive clinical operations experience, especially in mental health, and possess strong project management skills, we’d love to see you thrive in our dynamic setting. This role is perfect for someone who can not only navigate the intricacies of clinical trials but also identify process improvements along the way. The position can be remote on the East Coast or hybrid in our New York City office, so you’ll have flexibility while being a crucial part of our groundbreaking work at Compass Pathways. Join us in our vision for a world of mental wellbeing and make a difference today!

Frequently Asked Questions (FAQs) for Associate Director, Clinical Trial Delivery (Temporary Contract) Role at Compass Pathways
What are the responsibilities of the Associate Director, Clinical Trial Delivery at Compass Pathways?

The Associate Director, Clinical Trial Delivery at Compass Pathways is responsible for overseeing the operational execution of clinical trials, ensuring adherence to timelines, budgets, and quality standards. This role involves managing relationships with clinical trial sites and vendors, developing trial-specific documents, monitoring trial progress, and resolving any arising issues. Additionally, the position includes leading and mentoring a small team of clinical operations professionals, contributing to process improvements, and ensuring compliance with all regulatory guidelines.

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What qualifications are required for the Associate Director position at Compass Pathways?

Candidates for the Associate Director, Clinical Trial Delivery position at Compass Pathways should ideally hold a Bachelor’s degree in a life sciences discipline and possess extensive experience in clinical operations. Particularly desirable is recent experience at a sponsor, as well as managing trials in mental health or neurology. A strong understanding of clinical trial regulations, excellent project management capabilities, and strong communication skills are also essential for success in this role.

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Is experience in mental health necessary for the Associate Director role at Compass Pathways?

While not strictly required, having experience in managing clinical trials specifically within the field of mental health is preferred for the Associate Director, Clinical Trial Delivery role at Compass Pathways. This experience provides valuable insight into the unique challenges and regulations associated with mental health studies, which is crucial for successfully overseeing the innovative trials we conduct.

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How can the Associate Director ensure compliance during clinical trials at Compass Pathways?

The Associate Director, Clinical Trial Delivery at Compass Pathways ensures compliance by maintaining accurate and complete trial documentation, adhering to established regulatory guidelines, and implementing robust processes for trial conduct. Regular audits and training for the clinical operations team also contribute to a compliance-focused culture, enabling smooth trial progression while adhering to legal and ethical standards.

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What is the duration of the Associate Director, Clinical Trial Delivery position at Compass Pathways?

The Associate Director, Clinical Trial Delivery position at Compass Pathways is a temporary contract role expected to last until December 31, 2025. This provides a unique opportunity to contribute to pioneering trials in mental health treatment during a significant period of innovation within the company.

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Common Interview Questions for Associate Director, Clinical Trial Delivery (Temporary Contract)
Can you explain your experience managing clinical trials?

In answering this question, be specific about the types of clinical trials you've managed, including any key metrics or results achieved. Highlight your role in maintaining budgets and timelines, and demonstrate your problem-solving abilities when challenges arose.

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How do you ensure compliance with clinical trial regulations?

Clearly outline your understanding of compliance standards and regulations. Discuss specific experiences where you implemented or improved processes to ensure adherence, and mention any training programs you’ve developed or participated in.

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What strategies do you use to build team collaboration in clinical operations?

Describe your approach to fostering teamwork, including any tools or methods you’ve used, like team-building activities or collaborative project platforms. Share an example of how this has positively affected a previous project.

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Can you share a time you improved a clinical trial process?

Provide a specific example where you identified inefficiencies in a clinical trial process and successfully implemented changes that led to time or cost savings, or improved participant outcomes. Use metrics to quantify your impact where possible.

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How do you deal with conflicts between stakeholders during clinical trials?

Discuss your approach to conflict resolution by emphasizing communication, active listening, and negotiation skills. Share a relevant example that showcases your ability to mediate effectively and reach a satisfactory outcome for all parties.

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What tools or software have you used in managing clinical trials?

Mention any Clinical Trial Management Systems (CTMS) or electronic data capture tools you are familiar with, discussing your proficiency and how these tools improved trial efficiency and data integrity in your past roles.

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How do you keep up-to-date with industry regulations and standards?

Explain your methods for staying current with industry developments, such as attending conferences, subscribing to relevant journals, or participating in professional organizations. Highlight how this knowledge translates into best practices in your work.

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What specific challenges do you think you might face in this role?

Identify potential challenges, such as participant recruitment or regulatory changes, and present well-thought-out strategies for overcoming them. This shows your proactive mindset and readiness for the role.

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How do you prioritize tasks when managing multiple clinical trials?

Share your methods for prioritization, possibly involving task management systems or time management techniques. Use a real-life example to illustrate how you effectively handled competing demands while maintaining quality and compliance.

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What motivates you to work in the clinical trial space, particularly in mental health?

Express your passion for improving patient outcomes and highlight any personal or professional experiences that drive your commitment to mental health. Connecting this motivation back to Compass Pathways’ mission can show your alignment with the company’s values.

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MATCH
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FUNDING
DEPARTMENTS
SENIORITY LEVEL REQUIREMENT
TEAM SIZE
No info
HQ LOCATION
No info
SALARY RANGE
$160,000/yr - $240,000/yr
EMPLOYMENT TYPE
Contract, remote
DATE POSTED
March 26, 2025

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