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Senior/Clinical Project Manager
Il y a 22 minutes
In order to support our growth, we are looking to hire a Senior Clinical Project Manager.
As a Senior Clinical Project Manager you will be the driving force behind the successful execution of clinical trials for our sponsor clients. You’ll manage multiple studies across various therapeutic areas with a focus on oncology , ensuring delivery on time, within budget, and in full compliance with regulatory standards and the QMS system of DICE. Lead the planning, initiation, execution, and closure of clinical trials
Develop and manage project quotes, project timelines, budgets, and resource allocation
Monitor quality metrics and ensure continuous improvement
Oversee selection and management of third-party vendors, including contracting, budgets and invoices.
Operational oversight of clinical operations, regulatory and pharmacovigilance teams that are either contracted or collaborate on the projects
Team Leadership
Coordinate cross-functional teams including, biostatistician, data managers, medical monitors and medical writers
Provide guidance, mentorship, and performance feedback to project team members
Client & Stakeholder Management
Master’s degree in Life Sciences, Nursing, Biomedical sciences, Pharmacy, or related field or similar through experience.
Minimum 10 years of clinical research experience, with at least 5 years in a CRO project management role
Proven track record managing Phase I–IV trials across multiple therapeutic areas. Experience in oncology is considered as a plus.
Proficiency in project management tools (e.g., DICE is a clinical research organization (CRO), that supports clinical studies for pharmaceutical and biotechnology companies. We offer full service projects delivery to our sponsors, and have an internal team that is specialised in clinical data management, bio statistics, central imaging review, medical writing and medical monitoring.
Possibilities to work from home
A personal development path with tailored courses and training
