Company:
Signant Health
Industry: Pharmaceuticals
Deadline: Not specified
Job Type: Full Time
Experience:
Location: South Africa
Province:
Field: Project Management
As part of our team, your main responsibilities will:
- The Project Manager is responsible for the planning, execution and completion of projects considering budget, timelines, resources and task management. The Project Manager will communicate in a transparent and timely manner with the assigned Signant Health clients and internal stakeholders. He/she will manage project risks and ensure timely resolution while reporting out on project status with the appropriate internal and external stakeholders.
- The Project Manager contributes to the implementation of company-wide process improvements to ensure effective and efficient project delivery.
- This role requires an effective leader that excels in problem-solving, able to motivate a result-oriented team, and can build trust-based relationships with Signant Health’s clients.
You’ll need to bring:
- Bachelors’ degree or equivalent or relevant experience
- Understanding of the software development life cycle and the specification and configuration of software products
- Able to multi-task and work with multiple team members
- Must have excellent time management, communication (oral and written), and organizational skills
- Must be detail, and first-time quality delivery, orientated
- Must have solid MS Office Suite experience – Word, Excel, MS Project, PowerPoint
- Ability and experience of direct project activities and ensuring customer satisfaction while understanding and adhering to the study budget
- Must be comfortable speaking in front of diversified and/or large audiences
- Must be able to communicate and engage effectively with all levels of the organization and have excellent written and spoken English skills
- Must have experience in a Project Management role OR equivalent
- Must show initiative and be able to work independently as needed
Desirable:
- Background in Pharmaceutical, Medical education and/or CRO
- Experience of clinical trials/pharmaceutical industry/life sciences
- Ability to travel for business trips (overnight business trips could be expected quarterly)
- Experience/understanding of the clinical research environment and GCP principles is preferred
- PMP or equivalent certificate.
