Axsendo Clinical
PRN Clinical Research Coordinator Position
Axsendo Clinical, Portland, Oregon, United States, 97204
Join a Growing Team Where You Can Make a Difference - Clinical Research Coordinator Opportunity (Portland, Oregon)
Axsendo Clinical Research is seeking a motivated and detail-oriented Clinical Research Coordinator to join our nimble, patient-focused team on a part-time or PRN basis, with potential for transition to full-time based on performance and project needs.
If you're in the Portland, Oregon area and looking for a refreshing alternative to the structured pace of a large academic medical center or corporate setting, Axsendo offers an opportunity to work in a collaborative, agile environment where your voice is heard, and your contributions truly matter.
What We're Looking For:
A strong interest in clinical research, with a focus on improving patient care. Detail-oriented and proactive mindset. Flexibility and readiness to adapt to evolving project needs. Willingness to travel within the Portland area (minimal travel required). Why Join Axsendo?
Smaller, people-first company culture that values initiative and collaboration. Opportunities to learn and grow within a supportive environment. Ability to make an impact without the layers of bureaucracy found in larger organizations. If you're ready to take the next step in your clinical research career with a company that values your contributions and promotes growth, we'd love to hear from you.
Key Responsibilities:
Assist in the planning, execution, and monitoring of clinical trials. Coordinate and manage study-related activities, including patient recruitment and scheduling. Ensure compliance with regulatory requirements and study protocols. Collect, maintain, and manage study data and documentation. Collaborate with investigators, sponsors, and study team members. Participate in training and orientation of new staff and study volunteers. Conduct site visits and assist with patient follow-ups as needed. Prepare and administer IP Unblinded experience a plus. Qualifications:
Previous experience in clinical research or a healthcare setting is a plus. Strong organizational and multitasking skills. Excellent communication and interpersonal abilities. Proficient in Microsoft Office and data management software. Must be willing to travel within the Phoenix area as needed. Benefits:
Opportunity for professional growth and development. Potential for transition to a full-time role based on project needs and performance.
Axsendo Clinical Research is seeking a motivated and detail-oriented Clinical Research Coordinator to join our nimble, patient-focused team on a part-time or PRN basis, with potential for transition to full-time based on performance and project needs.
If you're in the Portland, Oregon area and looking for a refreshing alternative to the structured pace of a large academic medical center or corporate setting, Axsendo offers an opportunity to work in a collaborative, agile environment where your voice is heard, and your contributions truly matter.
What We're Looking For:
A strong interest in clinical research, with a focus on improving patient care. Detail-oriented and proactive mindset. Flexibility and readiness to adapt to evolving project needs. Willingness to travel within the Portland area (minimal travel required). Why Join Axsendo?
Smaller, people-first company culture that values initiative and collaboration. Opportunities to learn and grow within a supportive environment. Ability to make an impact without the layers of bureaucracy found in larger organizations. If you're ready to take the next step in your clinical research career with a company that values your contributions and promotes growth, we'd love to hear from you.
Key Responsibilities:
Assist in the planning, execution, and monitoring of clinical trials. Coordinate and manage study-related activities, including patient recruitment and scheduling. Ensure compliance with regulatory requirements and study protocols. Collect, maintain, and manage study data and documentation. Collaborate with investigators, sponsors, and study team members. Participate in training and orientation of new staff and study volunteers. Conduct site visits and assist with patient follow-ups as needed. Prepare and administer IP Unblinded experience a plus. Qualifications:
Previous experience in clinical research or a healthcare setting is a plus. Strong organizational and multitasking skills. Excellent communication and interpersonal abilities. Proficient in Microsoft Office and data management software. Must be willing to travel within the Phoenix area as needed. Benefits:
Opportunity for professional growth and development. Potential for transition to a full-time role based on project needs and performance.