Clinical Trials Program Lead

Upstate Medical University; City of Syracuse (NY); On-site; USD 72,000 - 75,000; Full time

Job summary

Upstate Medical University in Syracuse is seeking a Clinical Trials Program Lead to provide technical expertise and training to research staff. Responsibilities include coordinating Oncology trials, ensuring compliance with federal guidelines, and enrolling patients for trials.

The ideal candidate will possess a bachelor's degree with 4 years of relevant experience, excellent communication skills, and SoCRA or ACRP certification. Join a dedicated team focused on delivering high-quality cancer research.

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Qualifications

• Bachelor's degree and 4 years related experience or equivalent combination of education and experience.
• SoCRA or ACRP certification required.
• Oncology research experience required.

Responsibilities

• Provide day-to-day technical expertise and training to research staff.
• Perform program research tasks and coordinate Oncology research trials.
• Enroll, register, and screen patients for clinical research trials.

Skills

Excellent oral and written communication skills

Attention to detail

Ability to work independently

Ability to work within a team

Mentorship and leadership capabilities

Education

Bachelor's degree and 4 years related experience

SoCRA or ACRP certification

Oncology research experience

Job description

Job Summary

The Clinical Trials Program Lead provides day-to-day technical expertise and training to research staff, with mentorship and one-on-one support. They perform program research tasks such as filling out and approving study forms and documents and submitting Expanded Access Program requests. They coordinate Oncology research trials for the Cancer Center and satellite sites, involving investigational medications and FDA-regulated trials (early or late phase) with a high level of complexity, ensuring compliance with federal guidelines. They interact with clinicians, sponsors, cooperative groups, Upstate's Institutional Review Board, and regulatory agencies. They enroll, register, and screen patients for Oncology clinical research trials, collect and submit clinical trial patient data, and perform administrative duties including collection and shipment of lab samples and regulatory upkeep of clinical research study supplies.

Minimum Qualifications

• Bachelor\'s degree and 4 years related experience or equivalent combination of education and experience.
• Excellent oral and written communication skills and attention to detail.
• Ability to work independently and within a team, with mentorship and leadership capabilities.
• SoCRA or ACRP certification required.
• Oncology research experience required.

Preferred Qualifications

• Work Days: Monday-Friday (Days)

Salary and Recruitment

Salary Range: $72,000-$75,000

Recruitment Office: Human Resources