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Equivalent Experience
Description:
The Clinical Research Associate (CRA) will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements
Duration:
6 months 1099 or W2.
Skills:
Clinical research, oncology, cra
2+ years of clinical monitoring experience required. Knowledge of ICH and local regulatory authority regulations regarding drug Ability to travel Experience in monitoring all trial components (PSSV to COV) Experience in coaching/mentoring other CRA
Performance Expectations:
Protocols: 1-2 protocols could be 2 different sponsors. This group is only doing Oncology.
Days on Site: 8-10 days
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.
