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Sr. Cancer Research Program Coord

Building Name: UVMMC - UVM Given Building

Location Address: University of Vermont Campus, Burlington Vermont

Regular

Department: Hematology/Oncology II

Full Time

Standard Hours: 40

Biweekly Scheduled Hours:

Shift: Day

Primary Shift: -

Weekend Needs:

Salary Range: Min $26.76 Mid $33.46 Max $40.15

Recruiter: Naomi Kpesse

JOB DESCRIPTION:

The Senior Cancer Research Program Coordinator is responsible for working collaboratively with multi-disciplinary teams to manage an assigned portfolio of cancer clinical trials by coordinating and overseeing a variety of complex activities involved in collection, compilation, documentation, interpretation, and analysis of clinical research data. The position will manage the overall study coordination of a disease specific portfolio of cancer clinical trials including recruiting, screening, consenting, enrollment, study procedures, and follow up of patients. Serve as an essential member and co-leader of a multidisciplinary disease team in collaboration with the disease team leader. The position will also participate in quality assurance reviews of clinical trials.

Serve as a mentor, lead, and resource for Cancer Research Program Coordinators. Serve as a subject matter expert for the department. Provide training and educational programs for Cancer Research Program Coordinators. Provide coworkers with feedback to improve overall department performance. Collaborates with supervisor to design, implement, and direct day to day workflow of the department/division.

EDUCATION:

Associates Degree required; Bachelor’s degree preferred.

EXPERIENCE:

2+ years’ experience in clinical research or a combination of clinical research and oncology experience

Average salary estimate

$69583 / YEARLY (est.)
min
max
$55605K
$83561K

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 Sr. Cancer Research Program Coord, uvmhealth

If you're passionate about making a difference in the world of cancer research, then the role of Sr. Cancer Research Program Coordinator at the University of Vermont Medical Center (UVMMC) is tailor-made for you! Nestled in the vibrant community of Burlington, VT, this full-time position invites you to become a vital member of a multi-disciplinary team dedicated to advancing cancer clinical trials. As a Sr. Cancer Research Program Coordinator, you will take charge of a complex portfolio of trials, which means you’ll be conducting everything from recruiting and screening patients to overseeing their informed consent and enrollment. Your expertise will shine as you manage study procedures and maintain follow-up care, ensuring every detail is meticulously documented and analyzed. Collaboration is key; you’ll work closely with disease team leaders and other specialists, elevating the quality of care through comprehensive support and insight. Additionally, this role offers a fantastic opportunity to mentor and share your knowledge with other Cancer Research Program Coordinators. In doing so, you’ll not only assist with their professional growth but also help to improve overall department performance. With an eye on quality assurance, you’ll participate in reviews and offer valuable feedback. Ideal candidates will possess an Associate's degree (Bachelor’s preferred) and have at least 2 years of clinical research experience, ideally within oncology. Ready to embark on an impactful journey with UVMMC? We’d love to see how you can contribute to our mission!

Frequently Asked Questions (FAQs) for Sr. Cancer Research Program Coord Role at uvmhealth
What are the main responsibilities of a Sr. Cancer Research Program Coordinator at UVMMC?

As a Sr. Cancer Research Program Coordinator at the University of Vermont Medical Center (UVMMC), your core responsibilities revolve around managing a diverse portfolio of cancer clinical trials. You'll coordinate various intricate activities including patient recruitment, screening, consenting, enrollment, and follow-up. The role requires close collaboration with multidisciplinary teams, overseeing the logistics of study procedures, and ensuring the integrity of clinical research data is maintained through careful documentation and analysis.

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What qualifications do I need to become a Sr. Cancer Research Program Coordinator at UVMMC?

To qualify for the Sr. Cancer Research Program Coordinator position at UVMMC, an Associate's degree is required, while a Bachelor’s degree is preferred. More importantly, candidates should have at least 2 years of experience in clinical research or a relevant background that combines clinical research and oncology. This combination of education and experience is key to effectively manage and coordinate clinical trials.

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What role does mentorship play in the Sr. Cancer Research Program Coordinator position at UVMMC?

Mentorship is a significant aspect of the Sr. Cancer Research Program Coordinator role at UVMMC. In this position, you will not only lead your own portfolio but also serve as a mentor to other Cancer Research Program Coordinators. Your role includes providing training, guidance, and feedback, which is vital for fostering the growth and professional development of your colleagues within the department.

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How does collaboration impact the role of a Sr. Cancer Research Program Coordinator at UVMMC?

Collaboration is at the heart of the Sr. Cancer Research Program Coordinator's responsibilities at UVMMC. By working alongside multidisciplinary disease teams, you’ll actively participate in shaping clinical trial processes and ensuring the highest standards of patient care. This supportive teamwork environment allows for the sharing of insights and best practices, enhancing the quality and efficiency of cancer research.

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What is the expected work schedule for a Sr. Cancer Research Program Coordinator at UVMMC?

The Sr. Cancer Research Program Coordinator position at UVMMC is a full-time role, generally following a standard day shift schedule of 40 hours biweekly. This allows for a stable work-life balance while engaging in meaningful and impactful work in the cancer research field.

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Common Interview Questions for Sr. Cancer Research Program Coord
Can you describe your experience with clinical trials?

When answering this question, highlight any relevant clinical trial experience you have, detailing specific trials you've been involved in, your role in the process, and the outcomes. Describe the methods you used for patient recruitment, and data management, and how you ensured compliance with regulatory standards.

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How do you prioritize tasks when managing multiple clinical trials?

Discuss your approach to time management and prioritization. Provide examples of how you’ve effectively balanced the demands of multiple projects, perhaps using tools or techniques that help you stay organized and on track.

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What is your understanding of quality assurance in clinical research?

Provide a comprehensive overview of quality assurance principles in clinical research. Explain the significance of monitoring data integrity, compliance with protocols, and how you would address any discrepancies or issues that arise during trials.

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How do you handle difficult conversations with patients during the consent process?

Emphasize your communication skills and empathy. Share an example of a challenging situation where you successfully navigated a difficult conversation, ensuring patients felt informed and respected during the consent process.

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What motivates you to work in cancer research?

Share your personal motivation for entering the field of cancer research. This could be a personal story or professional reason that drives your passion for improving patient outcomes and contributing to medical advancements.

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How do you stay updated with the latest developments in oncology?

Discuss your commitment to continuous learning, such as attending relevant conferences, reading oncology journals, participating in webinars, or being part of professional networks that focus on oncology and clinical research.

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Describe how you would train a new Cancer Research Program Coordinator.

Outline your plan for onboarding and training a new team member, focusing on the mentorship aspect. Discuss the importance of providing them with resources, hands-on training, and regular feedback to help them succeed in their role.

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What strategies do you use to maintain accurate documentation in clinical research?

Highlight the importance of documentation in clinical trials and share specific strategies you have used to ensure accuracy and compliance, such as using well-defined templates, regular audits, and maintaining a checklist.

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Can you give an example of how you've contributed to a multidisciplinary team?

Provide an example that showcases your ability to work collaboratively within a multidisciplinary team. Explain how your input helped to drive the project forward and the value you brought to the team.

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How would you address a conflict within your team?

Describe your conflict resolution strategy, emphasizing the importance of communication, understanding different perspectives, and seeking a solution that benefits the project and team dynamics.

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EMPLOYMENT TYPE
Full-time, on-site
DATE POSTED
April 16, 2025

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