Apply on Employer Site

Boston Children's Hospital · 2 days ago

Clinical Research Assistant- Angelman Syndrome

Boston

Full-time

Hybrid

New Grad, Entry Level

$41K/yr - $61K/yr

Boston Children's Hospital is seeking a Clinical Research Assistant to assist with clinical research projects focusing on Angelman syndrome. The role involves coordinating clinical studies, recruiting participants, and managing study documentation under the supervision of the Principal Investigator.

Health CareHospitalMedical

Responsibilities

Assisting Principal Investigator (PI) in planning and implementing clinical research studies as assigned, including: coordinating preparation of protocol applications for submission to the IRB, study sponsor, regulatory authority, etc.; corresponding with the IRB, study sponsors, clinical research organizations, study participants, and referring physicians

Recruiting study participants for enrollment in clinical studies, including organizing strategies for recruiting study participants, screening study participants for eligibility, and completing informed consent procedures

Organizing study procedures and scheduling study participants for study visits. Assists the PI during study visits

Completing record abstraction of source documents, conducting required study measurements and completing study Case Report Forms (CRFs); conducting a QC check of completed CRFs prior to submission for data entry; coordinating resolution of all data queries

Maintaining regulatory binders, case report forms, source documents, and other study documents; monitoring the occurrence of adverse events and reporting to the PI, the study sponsor and the IRB, if any

Under the supervision of the PI, work with study staff to prepare for monitoring and audits by independent monitors, sponsors, and other regulatory agencies

Collection or processing of study specimens, delivery to appropriate labs or packaging and shipping to appropriate facilities

Assist PI and other study staff with conference presentations and manuscripts by extracting and compiling data from investigator-initiated studies