Oncology CRC II — Independent, Multi-Trial

PVH (Tommy Hilfiger/Calvin Klein); Fort Wayne (IN); On-site; USD 32,855 - 57,804; Full time

Job summary

Fort Wayne Medical Oncology and Hematology is seeking a Clinical Research Coordinator II (non-RN) to supervise and conduct complex clinical trials under medical supervision. The role requires independence and a strong grasp of protocol implementation across phase 1-3 designs.

Responsibilities include regulatory compliance, data integrity, budgeting and site feasibility, with annual trial accrual targets and patient-facing activities. Strong organizational skills are essential.

Qualifications

• Regulatory guidelines awareness (GCP/ICH)
• Clinical trial coordination and data handling
• Strong attention to detail and time management

Responsibilities

• Coordinate care for patients on clinical research protocols adhering to GCP/ICH.
• Assess subject eligibility and manage informed consent discussions per SOPs.
• Maintain accurate records of study materials, inventory, and regulatory documents.
• Support budgeting, contract processes, and sponsor communications for trials.
• Prepare and review safety reports and adverse event documentation.

Skills

Regulatory knowledge

GCP familiarity

Communication

Education

High school diploma

Some college / Bachelor's preferred

Licensed Practical Nurse preferred

Job description

Fort Wayne Medical Oncology and Hematology is seeking a Clinical Research Coordinator II (non-RN) to supervise and conduct complex clinical trials under medical supervision. The role requires independence and a strong grasp of protocol implementation across phase 1-3 designs.

Responsibilities include regulatory compliance, data integrity, budgeting and site feasibility, with annual trial accrual targets and patient-facing activities. Strong organizational skills are essential.