Clinical Research Nurse

Great chance to get into Clinical ResearchMonday-Friday schedule!Job DescriptionRecruit, 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

Additional Skills & QualificationsRegistered Nurse with license in Commonwealth of Pennsylvania; BSN preferred

Minimum of two to three years clinical research experience required

Experience with cancer medications and adverse event reporting using CTCAE 4.0 preferred.

Effective communication and writing skills; ability to multi-task and problem solve; demonstrated ability to work as part of a team as well as independently; knowledge of IRB and human research protection regulations

Must possess strong computer skills and be able to independently and proficiently work in MS office suite. Position contingent upon funding

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.