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Base pay range
Direct message the job poster from Skills Alliance Recruitment Consultant at Skills Alliance
*Clinical Project Manager - UK Remote - Full-Time - 6 month contract* Are you an experienced Clinical Project Manager interested in joining our biotech client that is leading the way in developing innovative CAR-T cell therapies for cancer treatment? We're hiring for a fast growing clinical-stage bio-pharmaceutical company at an exciting stage of development and would like to appoint a Clinical Project Manager, with experience in oncology/haematology who would be responsible for managing day to day operations of clinical trials, implementing study plans, and ensuring compliance with protocols, SOPs, and regulatory requirements. Key Responsibilities Coordinates with CROs and vendors Implements study plans developed by Sr. CPM/Principal CPM Maintains study timelines and tracks deliverables Monitors study progress and metrics Supports budget tracking and forecasting Manages protocol deviations and corrections Reviews monitoring reports Ensures TMF completeness and quality Experience Experience in haematology/oncology phase I/II studies Experience with ATIMPs and managing pivotal trials is an advantage Adept at working in a global setting and matrix environment Working knowledge of ICH-GCP and FDA/EMEA regulations If you're interested and would like to find out more, reach out on LinkedIn or send your CV to lewis.ray@skillsalliance.com Seniority level
Mid-Senior level Employment type
Contract Job function
Research, Project Management, and Science Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr
Direct message the job poster from Skills Alliance Recruitment Consultant at Skills Alliance
*Clinical Project Manager - UK Remote - Full-Time - 6 month contract* Are you an experienced Clinical Project Manager interested in joining our biotech client that is leading the way in developing innovative CAR-T cell therapies for cancer treatment? We're hiring for a fast growing clinical-stage bio-pharmaceutical company at an exciting stage of development and would like to appoint a Clinical Project Manager, with experience in oncology/haematology who would be responsible for managing day to day operations of clinical trials, implementing study plans, and ensuring compliance with protocols, SOPs, and regulatory requirements. Key Responsibilities Coordinates with CROs and vendors Implements study plans developed by Sr. CPM/Principal CPM Maintains study timelines and tracks deliverables Monitors study progress and metrics Supports budget tracking and forecasting Manages protocol deviations and corrections Reviews monitoring reports Ensures TMF completeness and quality Experience Experience in haematology/oncology phase I/II studies Experience with ATIMPs and managing pivotal trials is an advantage Adept at working in a global setting and matrix environment Working knowledge of ICH-GCP and FDA/EMEA regulations If you're interested and would like to find out more, reach out on LinkedIn or send your CV to lewis.ray@skillsalliance.com Seniority level
Mid-Senior level Employment type
Contract Job function
Research, Project Management, and Science Industries
Pharmaceutical Manufacturing and Biotechnology Research
#J-18808-Ljbffr
