01st July, 2025
Project Manager - Observational Clinical Studies - Real-World Data
Location: Remote - Europe / UK
Sector: Health Informatics | Real-World Evidence | Patient Registries
Ref: KEM-PM-RWE0625
Are you an experienced project manager passionate about advancing healthcare through real-world data?
KEMIO Consulting is supporting a leading health informatics company on a critical hire: a Project Manager to oversee complex clinical data projects in rare disease, oncology, and chronic conditions.
This is a unique opportunity to play a pivotal role in delivering patient-centric studies that are transforming how therapies reach the market. You\'ll be joining a mission-driven team focused on making real-world evidence matter.
What You\'ll Be Doing
This is more than a job - it\'s a chance to help reshape the future of healthcare by managing projects that directly support patients, researchers, and the life sciences industry. You\'ll thrive in a collaborative, fast-paced environment where innovation is encouraged and outcomes matter.
Apply now through KEMIO Consulting or contact us directly for a confidential discussion. #J-18808-Ljbffr
Project Manager - Observational Clinical Studies - Real-World Data
Location: Remote - Europe / UK
Sector: Health Informatics | Real-World Evidence | Patient Registries
Ref: KEM-PM-RWE0625
Are you an experienced project manager passionate about advancing healthcare through real-world data?
KEMIO Consulting is supporting a leading health informatics company on a critical hire: a Project Manager to oversee complex clinical data projects in rare disease, oncology, and chronic conditions.
This is a unique opportunity to play a pivotal role in delivering patient-centric studies that are transforming how therapies reach the market. You\'ll be joining a mission-driven team focused on making real-world evidence matter.
What You\'ll Be Doing
- Leading end-to-end delivery of study projects in line with protocols, contracts, SOPs, and timelines.
- Coordinating cross-functional teams to implement study plans, budgets, communication frameworks, and risk assessments.
- Managing large datasets and clinical deliverables using platforms like Wrike and RAID.
- Liaising with internal teams (e.g. Quality, Data Management, Biostats, Clinical Ops) to ensure clean, validated, and regulatory-compliant outputs.
- Communicating with sponsors, patient advocacy groups, and regulatory partners to ensure smooth delivery and strong engagement.
- Overseeing documentation, timelines, change requests, and master file integrity.
- Supporting innovation in real-world data platforms and patient registry design.
- Proven track record in observational clinical study project management - ideally within RWE, registries, or health data platforms.
- Strong knowledge of GCP/GPP, GDPR, HIPAA and global regulatory environments.
- Experience managing multi-functional project teams across Clinical, Biostats, Regulatory, Medical Writing, and Quality.
- Expertise in interpreting and acting on operational metrics/KPIs.
- Excellent communication and leadership skills with the ability to inspire cross-team collaboration.
- Proficiency in project management tools and documentation systems.
This is more than a job - it\'s a chance to help reshape the future of healthcare by managing projects that directly support patients, researchers, and the life sciences industry. You\'ll thrive in a collaborative, fast-paced environment where innovation is encouraged and outcomes matter.
Apply now through KEMIO Consulting or contact us directly for a confidential discussion. #J-18808-Ljbffr
