Find & Apply For Clinical Research Coordinator Jobs in Springfield, Massachusetts

Clinical Research Coordinator Voltaire Clinical Research Springfield, MA Job Details Full-time $26 - $30 an hour 1 day ago Benefits Health savings account Health insurance Dental insurance Flexible spending account Paid time off Vision insurance 401(k) matching Life insurance Qualifications Teamwork Clinical research Biostatistics Laboratory experience Phlebotomy specimen handling Patient care Organizational skills Full Job Description About Voltaire Clinical Research Voltaire Clinical Research is a patient-centered clinical research organization dedicated to advancing medical innovation through the successful execution of high-quality clinical trials across a broad range of therapeutic areas. We partner with sponsors, CROs, and healthcare providers to bring new treatments to patients while maintaining the highest standards of scientific integrity, regulatory compliance, and participant care. We are seeking an experienced and motivated Clinical Research Coordinator (CRC) to support the day-to-day execution of clinical trials at our research site. This role works closely with patients, investigators, sponsors, CROs, and other members of the research team to ensure studies are conducted safely, efficiently, and in accordance with study protocols and regulatory requirements. The site has a strong focus on nephrology and kidney-related clinical studies . The ideal candidate has at least two years of clinical research experience, is comfortable independently coordinating study activities, and enjoys working directly with patients. Previous nephrology or renal research experience is a plus but is not required. Key Responsibilities Coordinate the day-to-day execution of clinical research studies from study start-up through closeout. Conduct study visits and ensure all protocol-required procedures and documentation are completed accurately and on time. Participate in the informed consent process and ensure proper documentation is maintained. Support patient recruitment, screening, enrollment, scheduling, and retention. Perform phlebotomy and collect, process, and ship laboratory specimens according to study protocols. Obtain medical histories, vital signs, EKGs, and other protocol-required clinical information. Complete and maintain accurate source documentation and study records. Complete case report forms using paper and electronic data capture (EDC) systems and respond to data queries in a timely manner. Maintain investigational product accountability and assist with study drug dispensing when applicable. Identify, document, and report adverse events and serious adverse events according to study requirements. Ensure compliance with study protocols, Good Clinical Practice (GCP), FDA regulations, ICH guidelines, company SOPs, and applicable regulatory requirements. Maintain regulatory and essential study documentation. Coordinate and participate in site qualification, study initiation, monitoring, and closeout visits. Communicate effectively with investigators, sponsors, CROs, monitors, and other members of the research team. Support study timelines, enrollment goals, sponsor deliverables, and patient retention efforts. Maintain a patient-centered environment that prioritizes participant safety, confidentiality, and engagement. Assist with record retention and study archiving following study closeout. Qualifications Minimum of 2 years of Clinical Research Coordinator experience required Phlebotomy experience and proficiency required. Bilingual Preferred Experience independently coordinating clinical trials strongly preferred. Strong knowledge of Good Clinical Practice (GCP), FDA regulations, and clinical research operations. Experience with electronic data capture (EDC) systems. Strong organizational skills with the ability to manage multiple studies, patients, priorities, and deadlines. Excellent written and verbal communication skills. Strong attention to detail and commitment to accurate, timely documentation. Self-motivated, dependable, and accountable with the ability to work both independently and collaboratively. Strong patient-facing and interpersonal skills. Nephrology, renal, dialysis, or kidney-related clinical research experience is a plus, but not required. Experience in other patient-focused therapeutic areas such as cardiology, endocrinology, internal medicine, or similar specialties is welcomed. Clinical research certification such as ACRP, CCRC, CCRP, or equivalent is a plus. What We Offer Comprehensive benefits package. Opportunities for professional growth and development. Collaborative, patient-focused work environment. The opportunity to contribute to innovative clinical research that improves patient outcomes. Benefits 401(k) matching Dental insurance Flexible spending account Health insurance Health savings account Life insurance Paid time off Vision insurance

Work Location:

In person, 8am -5pm M-F with occasionally Saturday Applicants must be legally authorized to work in the United States and must not require current or future sponsorship for employment visa status. Voltaire Clinical Research is an Equal Opportunity Employer.

Pay:

$26.00 - $30.00 per hour Expected hours: 40.0 per week

Benefits:

401(k) matching Dental insurance Flexible spending account Health insurance Health savings account Life insurance Paid time off Vision insurance Application Question(s): Are you proficient in phlebotomy and comfortable independently performing blood draws on study participants? Do you have clinical research experience in nephrology, renal disease, dialysis, or kidney-related studies? Are you able to work onsite in Pontiac, MI OR Springfield, MA on a full-time basis?

Experience:

Clinical research: 2 years (Preferred)

Work Location:

In person