Clinical Research Coordinator: Study Operations & Patient Care

Alcanza Clinical Research, LLC; Boston (MA); On-site; USD 45,000 - 65,000; Full time

Benefits offered by this job

Medical, dental, vision insurance

401k with safe harbor match

Job summary

Alcanza Clinical Research, LLC is seeking a Clinical Research Coordinator to ensure compliant execution of studies. The role collaborates with site teams to screen, consent, and follow patients, while handling data entry in EDC and coordinating lab procedures.

Qualifications include a Medical Assistant diploma or equivalent with 1 year of clinical research experience, and proficiency in basic clinical procedures.

Qualifications

• Medical Assistant diploma or equivalent with at least 1 year of clinical research or clinical experience.
• Proficiency performing basic clinical procedures (blood pressure, vitals, EKGs, phlebotomy).
• Bi-lingual (English/Spanish) preferred.

Responsibilities

• Screen patients for study enrollment and obtain informed consent.
• Conduct patient follow-up visits and ensure data accuracy.
• Document in source clinics and enter data in EDC.
• Obtain vital signs and ECGs; perform basic lab procedures when needed.
• Maintain study supplies and logs; ensure timely SAE/Deviation reporting.

Skills

Clinical procedures

Bi-lingual English/Spanish

HIPAA knowledge

Microsoft Office & EHR

Strong communication

Detail-oriented

Independent worker

Education

Medical Assistant diploma

LPN/LVN credential

EMT credential

Associate’s degree

Tools

EDC systems

Job description

Alcanza Clinical Research, LLC is seeking a Clinical Research Coordinator to ensure compliant execution of studies. The role collaborates with site teams to screen, consent, and follow patients, while handling data entry in EDC and coordinating lab procedures.

Qualifications include a Medical Assistant diploma or equivalent with 1 year of clinical research experience, and proficiency in basic clinical procedures.