Clinical Trials Data & Regulatory Support Specialist

Indiana University; Indianapolis (IN); Vor Ort; USD 52.000 - 76.000; Vollzeit

Benefits dieser Stelle

Health insurance

Health Savings Account (HSA)

Flexible spending accounts (FSA)

Life insurance

Retirement plan

Tuition subsidy

Paid holidays

Paid time off

Employee assistance program (EAP)

Zusammenfassung

Indiana University Simon Comprehensive Cancer Center (IUSCCC) Clinical Trials Office seeks a committed professional to support and facilitate clinical research for adult and pediatric trials. The role includes coordinating visits, ensuring regulatory compliance, and maintaining data integrity across studies.

You will assist with recruitment, scheduling, and communications while staying current on best practices in clinical research.

Qualifikationen

• Bachelor's degree in science or health-related field with 1 year health-related or research experience.
• Associate's degree in allied health with 3 years health-related or research experience.
• Proficient written and verbal communication skills; professional demeanor.

Aufgaben

• Assist with identifying and recruiting potential research study subjects and determine eligibility per IRB/protocols.
• Coordinate study visits, screenings, consent, scheduling, and follow-up activities for participants.
• Record study data, samples, and results in databases and generate reports for investigators.
• Monitor compliance with SOPs and regulatory paperwork; communicate concerns to the PI.
• Support communications and materials development for recruitment and participant information.
• Stay current on regulatory affairs and best practices through ongoing education and meetings.
• Provide broader project support including budget, invoicing, and patient billing resolution as needed.

Kenntnisse

Communication skills

Professionalism

Time management

Quality focus

Flexibility

Dependability

Initiative

Relationship building

Ausbildung

Bachelor's degree in science/health

Associate's degree in allied health

Jobbeschreibung

Indiana University Simon Comprehensive Cancer Center (IUSCCC) Clinical Trials Office seeks a committed professional to support and facilitate clinical research for adult and pediatric trials. The role includes coordinating visits, ensuring regulatory compliance, and maintaining data integrity across studies.

You will assist with recruitment, scheduling, and communications while staying current on best practices in clinical research.