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Clinical Trial Associate

 

Location:         Boston

Reporting to:   Senior Director, Clinical Operations              

 

Job Summary

Orchard Therapeutics is a global biotechnology gene therapy company dedicated to transforming the lives of people affected by rare diseases through the development of innovative cell and gene therapies. Orchard has its global headquarters in London and its U.S. headquarters in Boston and is a wholly owned subsidiary of Kyowa Kirin, a Japan-based Global Specialty Pharmaceutical Company.

Reporting to the Director of Clinical Operations, the Clinical Trial Associate (CTA) will be responsible for providing project administrative and tracking support to the Clinical Study Managers for their assigned clinical studies. The CTA will be able to operate independently on certain CTA related tasks and exercise good judgement and decision making on what to bring to the study manager’s attention. The CRA will have the ability to take on increasing level of study manager responaibilities with guidance from the study manager. The CTA will also be responsible for supporting  individual studies, as well as participating in process improvement initiatives for the department.

This person will be key in supporting the clinical study day to day activities, to ensure on time delivery of main clinical milestones in accordance with ICH GCP as well as supporting general department activities and initiatives.

Key Responsibilities

·         Provide full support to the Clinical Study Managers and members of the Clinical Operations team as required

·         Maintain Sponsor Oversight Files for assigned studies and facilitate flow of documentation between sponsor and CRO-held TMF

·         Review & oversight of TMFs for the programs

·         Maintain study trackers to support Clinical Study Managers with oversight of study timelines, key milestones and progress reporting

·         Prepare and issue meeting minutes where required, including action items, under the direction of Clinical Study Managers

·         Collaborate with Finance on PO and invoice reconciliation to support Clinical Study Manager with oversight of study budget and financial reporting

·         Collaborate with other internal and external partners to faciltate communication, information and documentation flow as required (e.g. Regulatory Affairs, Clinical Science, central laboratory)

Experience ideally required

·         Experience & knowledge of supporting clinical trials, particularly co-ordination/administration

·         2-years CTA experience

·         Experience in working with CROs and vendors

Education / Key Competencies

·         BsC in life sciences or RN

·         Excellent organisational, interpersonal and communication skills and demonstrate the ability to work successfully in a team environment.

·         Able to work effectively in a fast-paced environment using different systems

·         Ability to prioritise and manage multiple tasks.

·         Confidently and accurately uses MSOffice and project management tools

·         ‘Can-do’ attitude and willingness to be flexible

·         Excellent decision making capabilities

 

 

Average salary estimate

$72500 / YEARLY (est.)
min
max
$60000K
$85000K

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 Clinical Trial Associate, Orchard Therapeutics

Join Orchard Therapeutics as a Clinical Trial Associate (CTA) and be a vital part of our mission to transform the lives of individuals affected by rare diseases through groundbreaking gene therapies. Located in the vibrant city of Boston, you will report directly to the Senior Director of Clinical Operations. In this role, you'll provide administrative and tracking support to our Clinical Study Managers, ensuring everything runs smoothly in our clinical trials. Your contribution will be significant, and you'll take pride in maintaining sponsor oversight files, reviewing TMFs, and keeping study trackers updated. Think of yourself as the glue that holds the team together! You'll play a crucial role in fostering communication among internal departments and external partners, so strong interpersonal skills are key. If you have at least two years of experience supporting clinical trials, especially in administration and coordination, we would love to hear from you. A Bachelor's degree in life sciences or nursing is essential along with a knack for organization and a proactive attitude. If you thrive in fast-paced environments and are ready to dive into the world of clinical research, then this CTA role at Orchard Therapeutics could be your next big adventure!

Frequently Asked Questions (FAQs) for Clinical Trial Associate Role at Orchard Therapeutics
What are the main responsibilities of a Clinical Trial Associate at Orchard Therapeutics?

As a Clinical Trial Associate at Orchard Therapeutics, you will provide crucial support to Clinical Study Managers by maintaining oversight files for assigned studies, reviewing Trial Master Files (TMFs), and preparing meeting minutes. Your role will require meticulous attention to study timelines and key milestones while facilitating communication between various departments such as Finance and Regulatory Affairs.

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What qualifications do I need to become a Clinical Trial Associate at Orchard Therapeutics?

To be considered for the Clinical Trial Associate position at Orchard Therapeutics, you should have at least a Bachelor's degree in life sciences or be a Registered Nurse (RN). Additionally, two years of relevant experience overseeing clinical trial coordination and administration is required, along with excellent organizational skills and proficiency in MS Office and project management tools.

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How does a Clinical Trial Associate contribute to clinical trials at Orchard Therapeutics?

A Clinical Trial Associate plays a key role in ensuring the smooth execution of clinical trials at Orchard Therapeutics. This includes supporting Clinical Study Managers, maintaining oversight documentation, tracking study progress, and reconciling budgets. You'll help ensure that trials meet their milestones in accordance with ICH GCP guidelines, making your input essential to the success of our research efforts.

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What work environment can I expect as a Clinical Trial Associate at Orchard Therapeutics?

Working as a Clinical Trial Associate at Orchard Therapeutics means you’ll be in a dynamic, collaborative environment. You will become part of a dedicated team that values communication and teamwork, striving to improve processes and achieve clinical milestones. Flexibility and a 'can-do' attitude are vital, as you will often juggle multiple tasks in a fast-paced setting.

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What personal qualities are important for a Clinical Trial Associate at Orchard Therapeutics?

As a Clinical Trial Associate at Orchard Therapeutics, it’s crucial to possess excellent interpersonal and communication skills. You should be detail-oriented, organized, and have the ability to prioritize effectively. A proactive mindset, willingness to adapt, and strong decision-making capabilities are also essential traits that will contribute to your success in this position.

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Common Interview Questions for Clinical Trial Associate
What experience do you have in supporting clinical trials?

When answering this question, be specific about your previous roles and responsibilities in clinical trial support. Highlight any relevant experience from your resume and be sure to mention any tools or systems you've used to manage trial documentation or timelines.

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How do you handle tight deadlines in a clinical setting?

Discuss your time management strategies and provide examples from your past roles. Show how you prioritize tasks and communicate with your team to ensure milestones are met effectively, even under pressure.

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Can you explain what a TMF is and its importance?

A Trial Master File (TMF) contains all essential documents related to a clinical trial. Explain that maintaining a complete and accurate TMF is vital for compliance and ensures that all regulatory and operational standards are met, which is crucial for the trial's success.

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How do you maintain organization while managing multiple tasks?

Share specific tools or methodologies you use, such as project management software or organizational strategies like to-do lists and prioritization frameworks. Illustrate with an example from your experience where your organization skills led to a successful outcome.

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Describe a challenge you faced in prior clinical trial work and how you resolved it.

Use this opportunity to showcase your problem-solving abilities. Clearly outline the challenge, your thought process in addressing it, and the ultimate resolution—focusing on what you learned from the experience.

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What role do you think communication plays in a clinical trial setting?

Discuss how clear and concise communication is critical in clinical trials to ensure alignment among team members and stakeholders. Mention your experience in collaborating with different departments and your strategies for facilitating effective communication.

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How do you stay updated on current clinical trial regulations?

Talk about your commitment to continuous learning. Mention specific resources like industry workshops, webinars, and articles that you follow to stay informed about the evolving landscape of clinical trial regulation principles.

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What steps would you take to ensure compliance with ICH GCP?

Explain your understanding of ICH GCP guidelines and outline practical steps you would take, such as regular audits of documentation and ongoing communication with study teams to identify and rectify compliance issues proactively.

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Why do you want to work as a Clinical Trial Associate at Orchard Therapeutics?

Express your passion for gene therapy and rare diseases, aligning your personal goals with the company's mission. Talk about the specific aspects of working at Orchard Therapeutics that excite you, such as their innovative approach to clinical research.

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How would you contribute to team dynamics in a clinical setting?

Highlight your ability to work collaboratively and adapt to a team environment. Share ways you’ve successfully contributed to team morale and productivity in previous roles, paved by open communication and support for colleagues.

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DATE POSTED
April 17, 2025

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