Oncology Clinical Research Assistant – Denver

Flourish Research; Denver (CO); On-site; USD 34,000 - 39,000; Full time

Benefits offered by this job

Health, dental, vision insurance

401(k) with employer match

Tuition reimbursement

Paid time off

Job summary

Flourish Research is hiring a Research Assistant for our Valkyrie Clinical Trials Denver site. The RA supports start-up, conduct, and close-out of oncology trial protocols, under supervision, ensuring accurate data and participant safety.

Responsibilities include reviewing protocols, documenting visits, obtaining informed consent, recruiting subjects, scheduling visits, and maintaining records in compliance with GCP and IRB requirements.

Qualifications

• Bachelor's degree in life sciences or related field preferred.
• 1-3+ years' experience in clinical or biological research; oncology experience is a plus.
• Excellent oral and written communication; proficient with Office 365.
• Professional, ethical, detail-oriented, and able to adapt to tasks.
• ECG and phlebotomy skills as required by protocol.

Responsibilities

• Read and understand protocols and assist with patient visits as directed.
• Document patient assessments, test results, and other data per regulations.
• Obtain informed consent according to regulations and IRB requirements.
• Assist in recruitment of qualified subjects to meet enrollment goals.
• Schedule, prepare, and conduct patient visits per protocol timelines.
• Maintain source documentation and complete case report forms accurately.
• Maintain confidentiality and communicate with study team per SOPs.
• Report adverse events to supervisors as needed.
• Assist in accountability of study materials and supplies.
• Participate in training and pursue educational opportunities.
• Represent Flourish Research professionally with stakeholders.

Job description

Flourish Research is hiring a Research Assistant for our Valkyrie Clinical Trials Denver site. The RA supports start-up, conduct, and close-out of oncology trial protocols, under supervision, ensuring accurate data and participant safety.

Responsibilities include reviewing protocols, documenting visits, obtaining informed consent, recruiting subjects, scheduling visits, and maintaining records in compliance with GCP and IRB requirements.