Research Coordinator Jobs in Arizona

Title: Clinical Science Program Specialist
Duration: 12 Months
Location: Tucson AZ 85755

The Opportunity

- Manages multiple clinical testing and lab services projects from initiation through contract completion under supervision of Program Manager.
- Acts as primary point of contact to Pharma customers.
- Performs tactical coordination of timelines for all projects and functions within CDx Pharma Services and:
- Develops project plans, establish and coordinates timelines for assigned projects and functions;
- Manages execution of cross-functional plans and tracks progress of activities;
- Identifies gaps, potential bottlenecks or delays and challenge assumptions.
- Oversees and guides day to day activities of sample process flow and accurate reporting of results.
- Implements / pulls in 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.
- Interfaces with resources outside of the company (Contract Research Organizations (CROs), site investigators, client counterparts, etc.) and serves as single point of contact with Pharma and clients.
- Manages meeting activities such as setting agendas, organizing meeting time and editing meeting minutes.
- Tracks, maintains and communicates project reports and clinical study data to Pharma and clients.

Requirements

- At least 2 years of project and/or clinical trial coordinator/management experience in a regulated, CRO, diagnostic, and/or pharmaceutical industry with regulated documentation.
- Exposure to clinical studies.
- Experience with clinical projects that require rapid activity/milestone achievement.
- Strong communication, collaboration, and organizational skills are required.
- Bachelor's degree is required (Life Sciences is preferred).

Preferred

- Previous experience with standard project management process (PMI) desired.
- Experience in clinical trial management and knowledge of bio-sample (clinical testing) management and process flow preferred.
- Preferred experience in clinical studies or companion diagnostics.
- Diagnostic and/or Pharmaceutical industry and relevant diagnostic area knowledge preferred.

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