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Description:
1. Conducts clinical trials in a manner that ensures compliance with AICR SOPs and policies, good clinical practices, FDA regulations, and study protocol
2. Participates in an integral way in the informed consent process by communicating clearly and openly with potential study patients about protocols open to enrollment
3. Possesses a thorough understanding of the study protocol(s) and answers all questions pertaining to the study posed during the informed consent process
4. Demonstrates ability to conduct a clinical trial from initiation to close in accordance with regulations, company policies and procedures
5. Maintains confidentiality of patient and/or protocol issues as appropriate and as bound by Confidentiality Agreements with AICR, between AICR and sponsors, and between AICR and other entities
6. Is creative and diligent in the recruitment of qualified study subjects into assigned protocols to fulfill enrollment obligations within the sponsor's timeline while following all policies and regulations governing medical ethics, IRB requirements, federal regulations/ICH guidelines, GCPs and AICR’s SOPs
7. Complies with all HIPAA regulations
8. Accurately assesses vital signs
9. Has training certificate in (or appropriate training in), and can competently perform, pediatric/adult phlebotomy
10. Obtains blood and urine samples and then processes and ships specimens as required.
11. Schedules patient visits according to protocol requirements and timelines
12. Able to accomplish protocol specified patient visits and procedures
13. Clearly and concisely documents patient assessments, observations, test results and other study related information per federal regulations/ICH guidelines, GCPs, AICR SOPs, sponsor/CRO and IRB requirements
Actalent connects passion with purpose. Our scalable talent solutions and services capabilities drive value and results and provide the expertise to help our customers achieve more. Every day, our experts around the globe are making an impact. We’re supporting critical initiatives in engineering and sciences that advance how companies serve the world. Actalent promotes consultant care and engagement through experiences that enable continuous development. Our people are the difference. Actalent is an operating company of Allegis Group, the global leader in talent solutions.
The company is an equal opportunity employer and will consider all applications without regards to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.
Other
$49k-66k (estimate)
12/17/2022
05/28/2023
The job skills required for Clinical Research Coordinator include Clinical Research, Coordination, Initiative, etc. Having related job skills and expertise will give you an advantage when applying to be a Clinical Research Coordinator. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Clinical Research Coordinator. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Clinical Research Coordinator positions, which can be used as a reference in future career path planning. As a Clinical Research Coordinator, it can be promoted into senior positions as a Clinical Research Manager that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Clinical Research Coordinator. You can explore the career advancement for a Clinical Research Coordinator below and select your interested title to get hiring information.