What are the responsibilities and job description for the Clinical Science Program Specialist position at IT ENGAGEMENTS, INC.?
Greetings from IT Engagements
IT Engagements is a global staff augmentation firm providing a wide-range of talent on-demand and total workforce solutions. We have an immediate opening for the below position with one of our premium clients.
Job Summary
Job Title: Clinical Science Program Specialist
Work Location: 1910 East Innovation Park Drive, Tucson, AZ USA - 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 Roche 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 Roche 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.
Regards,
Satya