Real World Evidence (RWE) Associate Project Manager
Real World Evidence (RWE) Associate Project Manager
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Job Description
For our Real World Solutions Team based in Prague we are looking for a Real World Evidence (RWE) Associate Project Manager.
Open Position Description
IQVIA is seeking a dynamic and experienced Associate Project Manager to lead and coordinate Real World Evidence (RWE) projects in the Czech Republic and CEE region. This role is ideal for a professional with vertical expertise in RWE including observational studies patient registries and clinical protocol development who can manage cross-functional teams and ensure successful project delivery.
Responsibilities:
- Coordinate organize and plan observational study activities managing timelines and projects quality while ensuring projects are delivered on budget
- Manage consistency of data sources with direct interactions with all the actors involved in the studies
- Coordinate junior IQVIA resources and external stakeholders (from the clinical side)
- Oversee (from a PM perspective) all activities related to CRF systems protocol definition patient registries relations with clinical sites etc.
- Manage clients communication
- Help organizing the work of junior team members and ensuring quality controls on projects
- Collaborate with internal and external stakeholders to define project scope timelines and deliverables.
- Ensure compliance with clinical protocols regulatory requirements and IQVIAs quality standards.
- Manage project budgets timelines and resources ensuring optimal allocation and performance.
- Serve as the primary point of contact for clients providing regular updates and strategic guidance.
- Coordinate with data management biostatistics medical writing and regulatory teams to ensure seamless project execution.
- Identify risks and implement mitigation strategies to ensure project success.
Requirements
- Bachelors or Masters degree in Life Sciences Public Health Pharmacy or a related field with deep expertise on clinical research world
- 3 years working experience in project management within the healthcare or life sciences industry preferably in RWE or observational research (CROs regulatory Pharmacovigilance)
- Ability to coordinate projects and resources
- Good expertise on clinical data management
- Excellent Microsoft Office Skills: strong skills in working with Excel and Power Point
- Proficiency in English and Czech both oral and written
- Strong communication skills both oral and written
- Ability to manage multiple projects juggle priorities and deliver on tight deadlines
- Affinity for a collaborative team-oriented environment
- Critical thinking and problem-solving attitude
Location: Prague Hybrid contract
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
Required Experience:
IC
Employment Type
Full-Time
