Digital Project Coordinator
hace 1 mes
Unlock a World of Opportunity
At Signant Health, we're pushing the boundaries of innovation in evidence generation. As a global leader, we empower our customers to digitally transform their clinical trial programs.
This is your chance to be part of a dynamic team that's shaping the future of healthcare. As a Digital Project Coordinator, you'll play a vital role in ensuring the success of our projects by coordinating and managing multiple tasks, collaborating with cross-functional teams, and driving project delivery forward.
About the Role:
- Coordinate and lead initial project delivery tasks, including software development lifecycle (SDLC) management for simple to medium complexity studies.
- Ensure project systems are built and released according to client expectations, leading the project system change control process.
- Support implementation of complex, multi-product projects as needed.
- Manage projects within established timelines, budget, quality standards, and contractual requirements.
- Review, approve, and maintain project and corporate systems and documentation.
- Handle client escalations independently, working with internal and client teams to resolve issues promptly.
- Communicate effectively with clients, serving as the primary contact for assigned projects.
- Accountable for financial health of assigned projects, including vendor services, licensing, payments, invoicing, devices, resource assignments, and vendor management activities.
- Collaborate with other functional areas to ensure timely delivery and meet client expectations within budget.
- Responsible for identifying and documenting incident reports with the Quality Management group, including client notification and closure.
- Report project status updates to stakeholders.
- Embody a culture of process improvement, focusing on streamlining processes to add value to our business and meet client needs.
Your Skills and Qualifications:
- Bachelor's degree or equivalent experience.
- Understanding of the software development life cycle and software product specification and configuration.
- Able to multitask and work effectively with multiple team members.
- Excellent time management, communication, and organizational skills.
- Detail-oriented, first-time quality delivery-focused.
- Proficient in MS Office Suite – Word, Excel, MS Project, PowerPoint.
- Ability to engage directly with clients, ensuring customer satisfaction while adhering to study budgets.
- Comfortable communicating with diverse audiences, having excellent written and spoken English skills.
- Experience in a project management role or equivalent.
- Show initiative and ability to work independently when needed.
We'd Love to See:
- Background in Pharmaceutical, Medical education, and/or CRO.
- Experience in clinical trials/pharmaceutical industry/life sciences.
- Ability to travel for business trips, including overnight stays (quarterly).
- Understanding of the clinical research environment and GCP principles.
- PMP or equivalent certificate.
Salary Range: $80,000 - $110,000 per year, depending on location and experience.
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