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
...sexual harassment, sexual assault, intimate partner and dating violence, and stalking for students and employees. The investigator serves... ...of sexual harassment, sexual assault, stalking, dating and domestic violence, and protected class discrimination and harassment involving...
...Renewable Natural Gas (RNG) Plant Operator Location: Malone, NY Employment Type: Full-time Sector: Renewable Natural Gas / Biogas About the Opportunity AD Energy Recruitment is supporting a growing Renewable Natural Gas (RNG) owner-operator with the hire...
...part of a team. Results-oriented with a focus on achieving and exceeding sales targets. Willingness to travel as needed. Must live in Orlando, Florida This position is salaried exempt, meaning that the successful candidate will not be eligible for overtime...
...Job Title: Sr Automated Test Engineer API Services Location: Denver, CO Duration: Long-term Interview Process: 1st Round : 30 Mints Video call 2nd Round : In-person interview About the Role We are looking for a Senior Automated Test Engineer to...
Location: Orange County, CA (On-Site) Employment Type: Full-Time | Exempt Role Description A privately held commercial real estate organization is seeking an experienced Property & Asset Operations Manager to support a growing portfolio of retail and mixed-use...