You are applying for a position through Medix, a staffing agency. The actual posting represents a position at one of our clients.

Job Summary

The Clinical Research Coordinator (CRC) will work independently or under general supervision to manage and coordinate clinical research protocols. Reporting to the Director of Research and/or Principal Investigator (PI), the CRC will oversee the day-to-day operations of one or more concurrent clinical studies, ensuring compliance with research protocols, regulatory agency policies, and Good Clinical Practice (GCP) guidelines. This role will focus on clinical research in prostate and bladder oncology, including subject recruitment, data management, and coordination of all study-related activities.

Key Responsibilities

• Execute and manage all phases of clinical research protocols, ensuring adherence to specific study requirements.
• Coordinate data collection, specimen handling, and study operations across multiple departments and services.
• Maintain accurate and timely documentation, adhering to local, state, and FDA GCP regulations.
• Serve as the point of contact for investigators, sponsors, and study personnel, ensuring effective communication and collaboration.
• Perform data entry, create and manage databases, and ensure accuracy in study results and reporting.
• Assist in protocol renewals, modifications, and the implementation of new clinical studies.
• Identify and screen eligible participants, including case and control subjects, for study inclusion.
• Travel to various Urology San Antonio offices as required.
• Adapt to changes within the growing research department and evolving study demands.

Qualifications

• High attention to detail with excellent organizational skills.
• Strong written and verbal communication abilities.
• Ability to work independently and manage multiple projects.
• Proficiency in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint).
• At least 3-5 years of experience in clinical research, with experience managing operations, coordinating patient visits, and supporting PIs.
• Knowledge of oncology treatments and the purpose of medications used in cancer care.
• Clinical research certification (e.g., ACRP, SOCRA) is a plus.
• Bachelor's degree in a science-related field (e.g., biology, life sciences) or equivalent experience.

Skills

• Proficiency in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint).
• Strong written and verbal communication abilities.
• High attention to detail and excellent organizational skills.
• Patient & Customer Focus: Demonstrates a strong commitment to patient care and satisfaction.
• Ethical Conduct: Maintains the highest standards of ethical behavior and confidentiality.
• Flexibility: Adapts to shifting priorities in a dynamic work environment.
• Initiative: Takes proactive steps to ensure study success.
• Personal Effectiveness/Credibility: Demonstrates reliability and integrity in all tasks.
• Stress Management/Composure: Handles pressure effectively while maintaining a positive attitude.

Additional Requirements

• Current Basic Life Support (BLS) certification.
• Three or more years of recent clinical research experience involving human participants.
• Previous experience in a facility offering similar services.

Medix Overview:

With over 20 years of experience connecting organizations with highly qualified professionals, Medix is a leading provider of workforce solutions for clients and candidates across the healthcare, scientific, technology, and government industries. Through our core purpose of positively impacting lives, we’re dedicated to creating opportunities for job seekers at some of the nation's top companies. As an award-winning career partner, Medix is committed to helping talent find fulfilling and meaningful work because our mission is to help you achieve yours.