Clinical Research Coordinator

The Clinical Research Coordinator at SI-BONE supports the clinical team in overseeing multiple clinical studies, ensuring compliance with best practices and quality assurance standards. This includes managing the Trial Master File, overseeing daily operations, preparing study documents, and ensuring all clinical sites adhere to research protocols.

While a Bachelor’s degree in life sciences is preferred, SI-BONE also values certifications such as the Association of Clinical Research Professionals. Candidates should be detail-oriented, proactive, and possess excellent verbal and written communication skills to excel in this dynamic role.

Essential skills for a Clinical Research Coordinator at SI-BONE include strong organizational abilities, effective multi-tasking, proficiency in Microsoft Office, and a commitment to ongoing quality control of clinical studies. Being a true team player is also pivotal in our collaborative environment.

SI-BONE maintains strict adherence to Good Clinical Practice (GCP) guidelines and continuously performs quality control audits on all studies. This commitment ensures that patient safety is prioritized and that all research practices align with the highest standards.

The working environment at SI-BONE is fast-paced, collaborative, and innovation-driven. Team members are encouraged to be creative and adaptive, working closely together towards the common goal of advancing solutions for sacroiliac joint conditions.

At SI-BONE, Clinical Research Coordinators are positioned for growth through mentorship, continuing education, and the dynamic nature of clinical research. Taking on broader responsibilities or moving into specialized roles in clinical operations can be pathways for advancement.

SI-BONE offers a competitive salary range of $72,000 to $80,000 for Clinical Research Coordinators, complemented by potential bonuses and stock options. Additionally, we prioritize employee well-being through benefits designed to support a healthy work-life balance.

When addressing conflicts within a clinical research team, it's essential to approach the situation with open communication. I would invite all parties to share their perspectives, aiming for a collaborative solution that aligns with our shared goal of patient safety and study integrity.

To ensure compliance, I meticulously review all study protocols, conduct regular audits, and provide training to team members on GCP guidelines. It's vital to create an environment where questions are encouraged, enabling us all to stay aligned with our compliance goals.

In my previous roles, I have been responsible for overseeing the Trial Master Files, which includes maintaining accurate documentation and ensuring that all files are updated in real time. I understand the importance of this role in ensuring a smooth audit process.

A successful Clinical Research Coordinator should be detail-oriented, proactive, and an excellent communicator. Balancing multiple responsibilities while maintaining thoroughness and adhering to timelines is essential in the fast-paced world of clinical research.

Effective communication with clinical sites is achieved through regular check-ins and clear documentation of all interactions. I also ensure that all requests from the sites are addressed promptly to foster a trusting and collaborative relationship.

To manage deadlines effectively, I prioritize tasks based on urgency and impact. I use project management tools to track progress across multiple studies, allowing me to allocate time efficiently while remaining adaptable to shifting demands.

Engaging clinical research staff starts with fostering a collaborative environment where everyone feels valued. I believe in setting regular team meetings to discuss progress and challenges while also providing opportunities for professional development.

To stay updated, I regularly attend professional conferences, participate in webinars and follow industry publications. Networking with fellow professionals also provides insights into emerging trends and innovative practices in clinical research.

One challenge I faced was managing site compliance issues. I overcame this by implementing a proactive monitoring system that identified problem areas early, allowing for timely interventions and maintaining study integrity.

I am motivated by the opportunity to improve patient outcomes and contribute to innovations in healthcare. Knowing that my work as a Clinical Research Coordinator has a direct impact on how patients are treated drives my commitment to excellence.