Greetings from IT Engagements
Role: Clinical Science Program Specialist (Contract W2 Role)
Location: Remote
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.
Thank You
vinaya [at] itengagements [dot] com