Clinical Research Associate (CRA)

• Assist in the management of the day to day operations of clinical trials including coordination and oversight of all CRO/clinical site/vendor activities, liaison between Clinical Operations Manager and CRO, manage scopes of work/budgets/invoice payments.

• Participate in development of protocol, case report form, CRF guidelines and other study documents.

• Prepare and/or review regulatory documents (e.g. ICF), contracts, requests for proposal.

• Ensure the training of CROs/investigators on protocol, regulatory, Client SOPs and data issues.

• Reviews and approves monitoring reports and ensures tracking of ongoing site issues.

• Minimum of college degree in a relevant discipline.

• Bachelors degree in relevant scientific discipline preferred.

• 1-2 years experience in pharmaceutical industry.

Sneha Shrivastava

Technical Recruiter (Clinical/Scientific)

Artech Information Systems LLC

360 Mt. Kemble Avenue, Suite 2000 | Morristown, NJ 07960

Office: 973.967.3348 | Fax: 973.998.2599

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