Job description

Our client, a world leader in life sciences and diagnostics, is looking for Clinical Services Project Manager I (100% Remote) based out of Tucson, AZ.

Duration: Long term contract (Possibility of further extension)

As Clinical Services Project Manager I, you will manage clinical and lab services projects from initiation through contract completion by applying project management skills and experience in delivering projects on time, within budget and with high customer satisfaction. You facilitate cross-functional interactions to complete the assigned projects within the deadline.

Responsibilities:

Managing clinical testing and lab services projects collaboratively, from initiation through contract completion.
Performing tactical coordination of timelines for all projects and functions within CDx Pharma
Services such developing project plans, establishing and coordinating timelines for assigned projects and functions; managing execution of cross-functional plans and tracking the progress of activities; identifying gaps, potential bottlenecks or delays and challenge assumptions and propose options to close gaps
Oversees and guides day-to-day activities of sample process flow and accurate reporting of results. Implements best practices within the clinical sciences team; fosters continuous improvement by ensuring knowledge and experience exchange.
Guides and manages cross-functional interactions to complete the assigned projects within the deadline.
Interface with resources outside of the company (Contract Research Organizations (CROs), site investigators, client counterparts, etc.) and serves as single point of contact with Pharma clients.

Education/Skills:

Bachelor's Degree in a related field or equivalent combination of education and relevant work experience.
2 years’ experience of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation.
Experience is in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow in the Diagnostic and/or Pharmaceutical industry.
Knowledge of clinical sample process flow and testing.
Proficiency with word processing, spreadsheet, database, and email software (e.g., Microsoft Excel, Microsoft Word).