YCCI Project Manager, Oncology

Remote Jobs; Teletrabalho; BRL 540.000 - 652.000; Tempo integral

Resumo da oferta

A leading remote healthcare organization is seeking an experienced clinical research professional to lead oncology clinical trials and manage research projects effectively. Applicants should possess a Bachelor's degree in a relevant field along with a minimum of four years of clinical research experience, knowledge of Good Clinical Practice (GCP) guidelines, and proficiency in Microsoft Office applications. This remote position offers a salary range up to $120,500 and the opportunity for career advancement within the organization.

Qualificações

• Bachelor's degree in a relevant academic/scientific field.
• Minimum of four years of experience in clinical research or a related field.
• Strong knowledge of Good Clinical Practice (GCP) guidelines and federal regulations.

Responsabilidades

• Oversee and lead the execution of project plans for oncology clinical trials.
• Manage a portfolio of research projects, ensuring compliance with standards.
• Conduct risk assessments and develop performance metrics to monitor progress.

Conhecimentos

Clinical research experience

Strong organizational skills

Knowledge of GCP guidelines

Proficiency in Microsoft Office

Formação académica

Bachelor's degree in a relevant field

Descrição da oferta de emprego

Why consider this job opportunity

• Salary range up to $120,500
• Opportunity for career advancement and growth within the organization
• Flexible remote work model
• Engage in impactful oncology research that contributes to improved patient outcomes
• Collaborative work environment with a focus on continuous process improvement
• Support for professional development and training in clinical research

What to Expect (Job Responsibilities)

• Oversee and lead the execution and implementation of detailed project plans for oncology clinical trials
• Manage a portfolio of research projects, ensuring compliance with regulatory standards and successful project completion
• Collaborate with faculty and staff to enhance administrative management of clinical studies
• Conduct risk assessments and develop performance metrics to monitor project progress
• Ensure effective communication among stakeholders, including sponsors, regulatory teams, and clinical operations

What is Required (Qualifications)

• Bachelor’s degree in a relevant academic/scientific field
• Minimum of four years of experience in clinical research or a related field
• Strong knowledge of Good Clinical Practice (GCP) guidelines and federal regulations
• Exceptional organizational skills with a strong attention to detail
• Proficiency in Microsoft Office programs (Word, Excel, PowerPoint, etc.)

How to Stand Out (Preferred Qualifications)

• Proven experience with oncology research
• Certification as a Clinical Research Associate or Clinical Research Professional (ACRP, SOCRA, or equivalent)

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