Description:

Must haves: Recruit, Screen, Enroll subjects in to clinical trails Explain Informed Consent process Document adverse events Collect study documents, protocols, regulatory documents, informed consents, case report forms and source documents Prepare the Institutional Review Board, IRB applications

Skills:

enrollment, Informed Consent, patient, oncology, patient consenting, clinical research coordinator, clinical trial, Gcp, Cra, Chart review, Clinical research, Clinical trial, Patient recruitment, Irb, Data entry

Top Skills Details:

enrollment, Informed Consent, patient, oncology, patient consenting, clinical research coordinator, clinical trial,Gcp,Cra,Chart review

Additional Skills & Qualifications:

BA/BS preferred - Experience with in-hospital clinical research -1- 3 years clinical research experience required - Experience with adverse event reporting -Experience with patient recruitment and consenting -Effective communication and writing skills -Knowledge of IRB and human research protection regulations

Experience Level:

Intermediate Level

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.