Senior Clinical Research Coordinator

Job Description

Job Description

Orso Health is a leading organization in clinical research, dedicated to advancing healthcare through innovative studies. We are committed to excellence in research and invite you to be part of our dynamic team. California and the Arizona market. Known for our high standards of excellence, we are committed to providing compassionate, patient-centered care for both pediatric and adult patients. Our dedicated team strives to improve lives through the expert diagnosis and treatment of a wide range of allergy and asthma conditions. We are looking for high-energy, kind, and collaborative individuals who are eager to grow personally and professionally to join our team.  

Position Summary

We are seeking a dedicated and experienced Senior Clinical Research Coordinator (CRC) to join our team. The ideal candidate will play a key role in managing clinical trials across multiple sites, ensuring compliance with regulatory requirements and study protocols while maintaining the highest standards of participant safety and data integrity. The position requires regular travel to study sites, making it essential for the candidate to be adaptable and organized.

This position requires some travel, with occasional support at our clinic sites in San Diego, Torrance, Long Beach, Scottsdale AZ. This role is non-exempt (hourly) and full-time, working 40 hours per week, Monday through Friday, Onsite in our El Centro Clinic. 

Key Responsibilities

Site Management:

• Oversee the day-to-day operations of clinical trials at various sites, ensuring adherence to study protocols, regulatory compliance, and good clinical practice (GCP).

Training & Mentorship:

• Provide training and support to junior CRCs and site staff, fostering a collaborative environment and ensuring proficiency in study procedures.

Participant Interaction:

• Engage with study participants, including recruitment, informed consent, and addressing any questions or concerns regarding the study process.

Data Collection & Documentation:

• Ensure accurate and timely collection, documentation, and reporting of study data in accordance with regulatory guidelines and sponsor requirements.

Regulatory Oversight:

• Maintain all necessary regulatory documentation, including IRB submissions, regulatory binders, and serious adverse event (SAE) reporting.

Sponsor & Stakeholder Communication:

• Act as the primary point of contact between the sponsor, study sites, and internal teams, facilitating effective communication and resolution of any issues that arise.

Quality Assurance & Compliance:

• Participate in site visits and audits, ensuring compliance with all study protocols and regulations.

Qualifications & Requirements 

Education:

• Bachelor's degree in a related field (e.g., life sciences, nursing, or similar).

Experience:

• Minimum of 5 years of experience in clinical research, with at least 2 years as a Clinical Research Coordinator.
• Experience in a variety of therapeutic areas is a plus.

Knowledge & Skills:

• Strong knowledge of GCP, FDA regulations, and clinical trial processes.
• Excellent organizational skills and attention to detail, with the ability to manage multiple projects simultaneously.
• Strong communication and interpersonal skills, capable of working collaboratively with diverse teams.
• Proven ability to work independently and handle challenging situations effectively.

Technology Proficiency:

• Proficient in using clinical trial management systems (CTMS) and electronic data capture (EDC) tools.

Travel:

• Willingness to travel frequently between sites as required.

Preferred Qualifications:

• Certification in clinical research (e.g., ACRP or SOCRA certification).

Benefits:

• Competitive salary and performance-based bonuses.
• Comprehensive health, dental, and vision insurance.
• Opportunities for professional development and continuing education.

Compensation

The hourly range for this position is $33.00-40.00/hour. The actual compensation for this role will be determined by a variety of factors, including but not limited to the candidate's skills, education, and experience.

Physical Requirements

Ability to stand, walk, and move throughout the clinic, if applicable, for extended periods; occasionally lift objects up to 25 lbs., bend, stoop, or reach as needed. Frequent use of hands and fingers for patient care and equipment operation. Must have normal (or corrected) vision and hearing and be able to respond quickly in a fast-paced clinical environment, if applicable.

What We Offer

• Competitive salary and benefits package, including medical, dental & vision insurance, 401(k) retirement plan with employer matching, and professional development opportunities
  • In addition, we offer paid time Off (PTO), sick time, floating holiday and holiday pay 
• Opportunity to shape the future of cutting-edge clinical research in beautiful San Diego (and across our expanding network)
• An opportunity to play an active role in medical advancement

If this role excites you, please submit your resume and a cover letter outlining your relevant experience and why you're passionate about joining our team. We look forward to hearing from enthusiastic candidates ready to drive our success!

California Consumer Privacy Act (CCPA) Notice
Orso Health ("OH") complies with the California Consumer Privacy Act ("CCPA"). Personal information provided in the job application process will be collected, used, and retained in accordance with applicable privacy laws. Candidates may request additional information regarding the categories of personal information collected and the purposes for which it is used during the hiring process.