Clinical Research Assistant Job at Elevate Clinical Research, Seabrook, TX

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  • Elevate Clinical Research
  • Seabrook, TX

Job Description

Job Description

Job Description

Salary: DOE

Research Assistant Expectations & Responsibilities
Participant Recruitment and Screening
Recruitment: Assist in identifying and recruiting study participants.
Screening: Conduct initial screening of potential participants to determine eligibility based on the study criteria.
Data Collection and Management
Data Collection: Capture data in CRIO using ALCOA-C and GCP guidelines.
Data Entry: Accurately enter data into Case Report Forms (CRFs) and electronic data capture systems.
Data Verification: Ensure the accuracy and completeness of data collected during the study.
Sample Collection: Assist with the collection, labeling, and processing of biological samples (e.g., blood, urine).
CRIO Task Management: Complete visits, progress notes, queries, and To-Dos in a timely and accurate manner according to ALCOA-C and GCP guidelines.
Study Coordination
Study Visits: Schedule and coordinate study visits for participants.
Informed Consent: Assist in obtaining informed consent from participants and ensure they understand the study procedures.
Documentation: Maintain detailed and accurate records of all study-related activities.
Participant Interaction
Communication: Serve as a point of contact for study participants, addressing their questions and concerns.
Follow-Up: Conduct follow-up visits and calls with participants to monitor their progress and collect additional data.
Support and Administration
Administrative Tasks: Assist with administrative tasks such as scheduling meetings, preparing study materials, and maintaining study supplies.
Collaboration: Work closely with the Principal Investigator (PI), Clinical Research Coordinators (CRCs), and other research staff to ensure the smooth operation of the study.
Reporting and Documentation
Reporting: Prepare and submit regular progress reports to the study team and sponsors.
Documentation: Ensure that all study documentation is organized, complete, and accessible for review and audits.
Training and Development
Training: Participate in training sessions and stay updated on new developments and best practices in clinical research.
Professional Development: Continuously seek opportunities for professional growth and development within the field.

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