Clinical Research Coordinator II (Data)

Data Manager (CRC II) ResponsibilitiesThe Clinical Research Coordinator II works under limited supervision, assists with running clinical trials, completes regulatory documentation and tracks IRB submission and approvals. May assist in the enrollment of human subjects. May provide clerical and technical support to ensure adherence to research protocols and quality of information received. Performs a variety of research, data base, biospecimen collection and processing, as well as clerical duties in support of clinical trials to assist investigators in organizing, gathering and compiling clinical research data.

Organizes and maintains documentation required for clinical trial(s).

Informs Principal Investigator and/or designated individual on any issues concerning patients response to treatment/medication/ any adverse effects overall to patients.

Assists Principal Investigator with regulatory body filings including IRB submissions.

May assist in the enrollment of human subjects.

May provide clerical and technical support to ensure adherence to research protocols and quality of information received.

About Actalent:

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.