Oncology Clinical Research Coordinator - Early Phase

START Center for Cancer Research; Grand Rapids (MI); Sur place; USD 52 000 - 68 000; Plein temps

Avantages offerts par ce poste

401(k) employer match

Performance bonus

Paid time off

Medical, dental, and vision coverage

Life and disability insurance

Employee Assistance Program

Flexible FSA/HSA

Résumé du poste

START Center for Cancer Research in Grand Rapids seeks a Clinical Research Coordinator to support early-phase oncology trials under senior staff guidance. You will ensure accurate conduct, adherence to protocols and patient safety, with direct patient interaction and data collection.

The role requires 2 years of clinical research experience, strong attention to detail, knowledge of GCP, and proficiency with Microsoft Office and trial management software.

Qualifications

• High School Diploma or GED required.
• 2 years of clinical research experience.
• Strong attention to detail and data accuracy.
• Working knowledge of GCP and regulatory requirements.
• Proficiency with Microsoft Office and trial management software.

Responsabilités

• Communicate with sponsors/CROs about protocol status and questions.
• Monitor day-to-day conduct of studies per protocol and GCP.
• Create/review forms to ensure protocol compliance.
• Maintain standardized trial documents and labeling.
• Train staff on protocols and amendments.
• Assist with patient screening and eligibility decisions.
• Facilitate informed consent process.
• Address protocol deviations with leadership.
• Support data coordination with case report forms and queries.
• Collaborate with PI to report Serious Adverse Events.

Connaissances

Clinical research

GCP knowledge

Data collection

Attention to detail

Microsoft Office

Formation

High School Diploma or GED

Outils

CTMS

Description du poste

START Center for Cancer Research in Grand Rapids seeks a Clinical Research Coordinator to support early-phase oncology trials under senior staff guidance. You will ensure accurate conduct, adherence to protocols and patient safety, with direct patient interaction and data collection.

The role requires 2 years of clinical research experience, strong attention to detail, knowledge of GCP, and proficiency with Microsoft Office and trial management software.