Clinical Research Coordinator (Research Assistant)
Onsite in Chapel Hill, NC
Contract till October 2026
The Research Assistant is responsible for supporting the lead coordinators in coordinating multiple complex trials through the protocol life cycles of activation, implementation and closure.
Specific Responsibilities:
Research Study Execution
* Collect study data through a variety of methods, per study protocol (e.g., administer surveys, observe/conduct study activities and record outcomes, electronic medical record data abstraction, biospecimens).
* Perform clinical tests and procedures in accordance with the study protocol, following adequate training.
* Record and organize study data and complete applicable case report forms (electronic or paper) as required in accordance with good clinical practice and ALCOA-C principles.
* Manage study visits as applicable (e.g., schedule/coordinate visits, prepare materials, manage research charges, etc.)
Research- Subjects/Ethics
* Maintain administrative study documentation (e.g., delegation of authority logs, training records)
* Assist in the development and submission of regulatory applications and/or study materials (e.g., recruitment materials, informed consent forms)
* Gather and store required regulatory documentation.
* Prepare for study monitoring, participate in monitoring visits, and assist with corrections as applicable.
* Track and document protocol deviations and adverse events.
Participant Management
* Screen and recruit study participants for studies per study protocol and applicable standard operating procedures.
* Obtain informed consent from study participants.
Research- Project Management
* Participate in basic study start-up activities.
* Participate in site initiation visits, study start-up meetings, and closeout visits for research studies.
Research- Quality Control
* Ensure accuracy of data collected by conducting quality assurance/quality control procedures.
* Report variations or discrepancies in data collected. Recognize discrepancies in patterns and make recommendations for process improvement.
Research- Lab Operations
* Maintain study supplies (e.g., laboratory kits, administrative supplies).
* Track and ship biospecimens, as applicable.
· Minimum Requirements
· One year of experience of patient facing clinical research experience
Preferred Qualifications
Experience in clinical research
EPIC medical records experience
...ARMStaffing is seeking a travel nurse RN ED - Emergency Department for a travel nursing job in Danville, Virginia. Job Description & Requirements ~ Specialty: ED - Emergency Department ~ Discipline: RN ~ Start Date: 11/10/2025~ Duration: 13 weeks ~36 hours...
...amenities, and the delightful details that make every visit feel personal and unforgettable. What will you do in this job? Safety,... ...dynamic guest service at the Talkeetna Alaskan Lodge. As Sous Chef, you will oversee and participate in the preparation of menu items...
Job Quick Facts: Specialty: Physical Medicine and Rehabilitation. Job Type: Locum Tenens. Location: Colorado Springs, CO. Service Setting: Inpatient. Reason For Coverage: Supplemental. Coverage Period: ASAP - Ongoing. Coverage Type: Clinical Only. ...
...the Patient Services Manager and the direction of the Clinical Nurse, performs specific duties that support patient care. These duties... ...or GED; and CNA or other educational equivalent, i.e. Medical Assistant, Phlebotomy Technician, Student Nurse who has completed one...
Make cash from Home by Participating in Surveys - Data Entry - Customer Service Representative - Part TimeWe are looking for people nationwide to join paid studies - Apply ASAP... ...determine your own participation schedule. At this work, you will be doing different tasks such as...