Axsendo Clinical
Clinical Research Coordinator in Phoenix
Axsendo Clinical, Phoenix, Arizona, United States, 85003
About Us
At Axsendo Clinical Research, we believe that successful clinical trials are built on true partnerships. We are deeply invested in the journey from discovery to delivery, with a singular focus on advancing life-changing medical therapies. Every aspect of our work centers around people-the patients we serve, the teams we support, and the processes we refine. Through this compassionate and dedicated approach, we aim to transform the landscape of medical treatment and access to healthcare.
Position Overview
We are seeking an experienced Clinical Research Coordinator (CRC) to join our team. The ideal candidate will have at least 3 years of clinical research experience, strong organizational and leadership skills, and a demonstrated commitment to patient care and research integrity.
This is an exciting opportunity to play a vital role in advancing clinical research while working closely with patients, investigators, sponsors, and cross-functional teams.
Key Responsibilities
Recruit, screen, consent, and enroll study participants while maintaining accurate and confidential records. Collect, process, and manage study data and specimens in compliance with study protocols and GCP. Support regulatory submissions (IRB applications, amendments) and assist compliance with required documentation. Coordinate daily study activities, including scheduling, monitoring visits, and ensuring protocol adherence. Collaborate with investigators, sponsors, and internal teams to ensure seamless study execution. Assist with audits, monitoring visits, and quality checks to ensure ongoing regulatory compliance. Qualifications
Bachelor's degree in a health-related field preferred. Minimum 3 years of clinical research experience required. CCRC or ACRP certification preferred. Strong organizational and communication skills. Phlebotomy experience required. Skills
Proficiency in phlebotomy and specimen handling techniques. Experience with CTMS (CRIO preferred but not required). Strong organizational and time-management skills with the ability to manage multiple priorities. Excellent verbal and written communication abilities. Proficiency in Microsoft Office Suite and clinical research software. Ability to work independently and collaboratively within a multidisciplinary team. Detail-oriented with a strong commitment to accuracy, compliance, and research integrity. Prior experience in Pulmonology, Podiatry, or Cardiology preferred. Other Requirements
Valid driver's license and reliable transportation for travel between local offices. Flexibility to adjust work hours Monday-Friday as protocol or subject visits require. Benefits
Competitive pay with opportunities for advancement. Paid time off and company holidays.
At Axsendo Clinical Research, we believe that successful clinical trials are built on true partnerships. We are deeply invested in the journey from discovery to delivery, with a singular focus on advancing life-changing medical therapies. Every aspect of our work centers around people-the patients we serve, the teams we support, and the processes we refine. Through this compassionate and dedicated approach, we aim to transform the landscape of medical treatment and access to healthcare.
Position Overview
We are seeking an experienced Clinical Research Coordinator (CRC) to join our team. The ideal candidate will have at least 3 years of clinical research experience, strong organizational and leadership skills, and a demonstrated commitment to patient care and research integrity.
This is an exciting opportunity to play a vital role in advancing clinical research while working closely with patients, investigators, sponsors, and cross-functional teams.
Key Responsibilities
Recruit, screen, consent, and enroll study participants while maintaining accurate and confidential records. Collect, process, and manage study data and specimens in compliance with study protocols and GCP. Support regulatory submissions (IRB applications, amendments) and assist compliance with required documentation. Coordinate daily study activities, including scheduling, monitoring visits, and ensuring protocol adherence. Collaborate with investigators, sponsors, and internal teams to ensure seamless study execution. Assist with audits, monitoring visits, and quality checks to ensure ongoing regulatory compliance. Qualifications
Bachelor's degree in a health-related field preferred. Minimum 3 years of clinical research experience required. CCRC or ACRP certification preferred. Strong organizational and communication skills. Phlebotomy experience required. Skills
Proficiency in phlebotomy and specimen handling techniques. Experience with CTMS (CRIO preferred but not required). Strong organizational and time-management skills with the ability to manage multiple priorities. Excellent verbal and written communication abilities. Proficiency in Microsoft Office Suite and clinical research software. Ability to work independently and collaboratively within a multidisciplinary team. Detail-oriented with a strong commitment to accuracy, compliance, and research integrity. Prior experience in Pulmonology, Podiatry, or Cardiology preferred. Other Requirements
Valid driver's license and reliable transportation for travel between local offices. Flexibility to adjust work hours Monday-Friday as protocol or subject visits require. Benefits
Competitive pay with opportunities for advancement. Paid time off and company holidays.