Clinical Research Coordinator I - Patient-Centric Trials

Iterative Scopes; City of Albany (NY); On-site; USD 65,000 - 90,000; Full time

Job summary

Iterative Health is hiring a Clinical Research Coordinator I to help run day-to-day clinical trial activities and ensure patient safety and protocol compliance. You will work with sponsors, CROs, investigators, and internal teams to deliver high-quality trials and improve patient outcomes.

The role requires 1–3 years of clinical research experience, strong organizational skills, and the ability to perform blood draws and EKGs in line with state regulations.

Qualifications

• Associate’s or Bachelor’s degree in a scientific, healthcare, or related discipline required.
• 1–3 years of clinical research or healthcare experience required.
• Must be able to perform blood draw, medical review (blood pressure, height, weight etc.) & EKGs, as applicable by state law.
• Strong organizational skills and attention to detail.
• Ability to manage competing priorities in a fast-paced environment.
• Ability to read, interpret, and apply research protocols and clinic policies.
• Proficiency with standard office software and willingness to learn clinical research systems.
• Familiarity with CTMS or EDC systems preferred.

Responsibilities

• Coordinate patient visits, procedures, and study-related activities in accordance with protocol requirements and study timelines.
• Support patient recruitment and outreach, scheduling, and informed consent coordination.
• Conduct protocol-required patient visits and assessments in accordance with study protocols, GCP guidelines, and SOPs.
• Perform protocol-required clinical procedures including vital signs, ECGs, specimen collection, and investigational product accountability.
• Maintain accurate and timely study documentation including source records and CTMS updates.
• Maintain high-quality data entry and timely resolution of data queries.
• Serve as a point of contact for study participants throughout participation.
• Support preparation for sponsor, CRO, and regulatory monitoring visits.

Skills

Blood draw

EKGs

Organizational skills

Attention to detail

Communication

Education

Associate’s degree

Bachelor’s degree

Tools

CTMS

EDC systems

MS Office

Job description

Iterative Health is hiring a Clinical Research Coordinator I to help run day-to-day clinical trial activities and ensure patient safety and protocol compliance. You will work with sponsors, CROs, investigators, and internal teams to deliver high-quality trials and improve patient outcomes.

The role requires 1–3 years of clinical research experience, strong organizational skills, and the ability to perform blood draws and EKGs in line with state regulations.