Clinical Research Assistant II - IBD

Children's Hospital of Philadelphia•Philadelphia, PA

7d•$23 - $29•Onsite

About The Position

The Inflammatory Bowel Disease Center is seeking a full-time Clinical Research Assistant II (CRAII) to join a highly productive team focused on conducting a variety of research projects to understand inflammatory bowel disease (IBD), advance current treatments, improve quality of life, develop new therapies and find a cure for IBD. Under the supervision of the clinical research administrative director and/or Principal Investigator, the CRAII responsibilities include recruitment of research participants, informed consent, interfacing with clinical care and lab staff to schedule research visits, ensuring adherence to study protocols, and collecting and entering data into clinical study databases. This position will work closely with the lead clinical research coordinator to assist successful recruitment of subjects and collection of biospecimens during clinical procedures (such as colonoscopies, surgery). Excellent communication, organizational, and time-management skills are important. Under the direct supervision of the Principal Investigator and/or other study team members, this role provides experienced support in the conduct of clinical research. Job responsibilities may include human subject research activities including subject enrollment, data/sample collection, data entry, and regulatory submissions support.

Requirements

High School Diploma / GED Required
At least one (1) year of relevant clinical research experience Required
Basic knowledge of IRB and human subject protection.

Nice To Haves

Bachelor's Degree Preferred
At least two (2) years of relevant clinical research experience Preferred

Responsibilities

Providing technical and clinical support in the conduct of clinical studies
Filing and office organization
Patient/research participant scheduling
Patient/research participant history
Data collection/extraction from electronic medical record systems and entry into project databases and platforms
Data management, including assisting with quality control and data review
Laboratory procedures
Research Study Compliance
Adhere to IRB approved protocols and compliance with HIPAA and handling confidential materials
Support the safety of clinical research patients/research participants
Comply with Institutional policies, SOPs and guidelines
Comply with federal, state, and sponsor policies
Participate in the informed consent process for study subjects
Document and report adverse events
Maintain study source documents
Submit basic IRB reports
Assist with IRB/regulatory submissions
Complete case report forms (paper and electronic data capture)
Follow-up care
Order materials/supplies
Schedule research meetings