Description:

Job Responsibilities:

- Majority source verifying and data monitoring studies

- Monitoring data and reviewing data for accuracy and protocol compliance for Investigator initiated trials

- Reviewing the data (Not pharmacy or regulatory )

- Study start up/implementation and maintenance

- Review protocols before SRC and IRB (From QA standpoint to make sure they make they correctly written)

- Get the SIV up and running (as the protocol opens we will collect all Serious adverse/Adverse events data )

- Admin work maintaining files for the DMC

- Perform Internal auditing of our IITs

*Remote flexibility*

Qualifications:

Experience as a CRC

Experience in Oncology (1-3 years)

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. Were 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.