Study Start Up Analyst

We are looking for 2 Study Start Up Analysts on a contractual basis for a large CRO in Durham, NC.

The position will start immediately and last 6 months to hire.

Description:

The Analyst II role is to efficiently and expertly perform start up activities inclusive of site regulatory document collection, CSA negotiations, and clinical document review services (review clinical investigator site regulatory package documents, and protocols as related to informed consent forms). Participate in assigned Clinical Operations initiatives aimed at improving internal standards and systems. Also to mentor to Analyst I and Associate level staff.

Education:

4-year degree or relevant clinical or business equivalent.

Requirements:

Minimum of 2-3 years work experience, one of which has been involved in contract negotiation, site regulatory document collection and review, have performed start up activities and/or clinical site monitoring.

Skills: Demonstrated ability to successfully manage a full workload across multiple-projectsAbove average interpersonal skillsAbility to understand and maintain client confidentialityInterpersonal skills and ability to manage multiple projects requiredExtensive use of telephone and face-to-face communications which requires the accurate perception of speechComprehensive knowledge of relevant software:Windows, Word, Excel, Outlook. DatabaseExcellent negotiation skillsOrganized with solid oral and written communication skillsSolid analytical and problem-solving skills