Clinical Research Assistant - Oncology Trials Recruitment

Community Health Network; Indianapolis (IN); On-site; USD 42,000 - 56,000; Full time

Job summary

Community Health Network invites qualified candidates to join our Clinical Research Oncology Team as a Clinical Research Assistant. The role involves recruiting, screening, interviewing and consenting patients per protocol, plus data entry and study documentation.

You will support coordinators and investigators and assist with administrative tasks for clinical trials. We value strong communication, healthcare experience, and attention to detail.

Qualifications

• Demonstrates knowledge of patient care process.
• Adheres to hospital policies and procedures.
• Excellent written and verbal communication to varied audiences.
• Interacts with people from diverse backgrounds.
• Demonstrates strong organizational and time management skills.
• Proficient computer skills: Word, Excel, Outlook, EMR.
• Minimum 1–2 years of healthcare experience.
• High school diploma or equivalent.
• Medical Assistant or Medical Office Assistant experience preferred.

Responsibilities

• Recruit, screen, interview and consent study patients per protocol.
• Complete study-related documentation and data entry.
• Assist with administrative duties for clinical trials and department support.
• Maintain data management system to track patient recruitment.
• Collect, process and ship specimens per protocol and regulations.

Skills

Patient care process

Compliance with standards

Communication skills

Diversity awareness

Organizational skills

Time management

MS Word

MS Excel

MS Outlook

EMR

Healthcare experience

Education

High school diploma or equivalent

Medical Assistant or Medical Office Assistant training

Tools

MS Word

MS Excel

MS Outlook

EMR

Job description

Community Health Network invites qualified candidates to join our Clinical Research Oncology Team as a Clinical Research Assistant. The role involves recruiting, screening, interviewing and consenting patients per protocol, plus data entry and study documentation.

You will support coordinators and investigators and assist with administrative tasks for clinical trials. We value strong communication, healthcare experience, and attention to detail.