A global CRO specializing in dermatology is looking for a Clinical Project Manager to oversee and manage multi-center clinical trials. This remote role requires at least 6 years of industry experience, including managing dermatology trials. The ideal candidate will lead project teams and ensure audit readiness while controlling budgets and timelines. Competitive salary of up to €100,000 plus bonus.
Qualifications
At least 6 years of industry experience, including a minimum of 3 years leading multi-center clinical trials (phase II-III).
Experience leading concurrent multi-centered clinical trials with budgets in excess of $3M USD.
Experience managing dermatology trials at Project Management level.
Responsabilités
Oversee and actively participate in the preparation of project deliverables.
Ensure assigned studies are 'audit-ready' at all times.
Control the project budget, focusing on internal hours allocated.
Lead the core project team and ensure adequate training.
Connaissances
Project management
Quality assurance
Risk management
Team leadership
Budget management
Description du poste
Overview
Clinical Project Manager - Dermatology (MUST HAVE EXPERIENCE WITHIN DERMATOLOGY AT PROJECT MANAGEMENT LEVEL)
Location: Germany (Remote)
Salary: Up to €100,000 plus bonus
My client is a full-service global CRO focusing on the therapeutic area of Dermatology. The founder of the business is a Medical Dermatologist and is therefore very passionate about these therapy areas.
With expansion in North America, Europe, Asia Pacific and Latin America, vast, continuously growing relationships with investigators and patients; and a dedicated research clinic through which we design and execute their studies.
Responsibilities
Project planning – Oversee and actively participate in the preparation of project deliverables, including study plans, protocols, informed consent forms, electronic case report forms (eCRFs), tables / listings / figures (TLFs), and clinical study reports.
Participate in the planning and conduct of the Investigator’s Meeting.
Ensure that each site has the necessary materials to perform the study (e.g., investigational product, study supplies, special equipment, safety lab kits, etc.).
Quality and risk management – Ensure assigned studies are “audit-ready” at all times.
Monitor the quality of study deliverables (including vendor and SubCRO deliverables) and address issues as they arise.
Manage risk and control measures to assure project quality.
Analyze discrepancies between planned and actual results.
Review and approve responses to quality assurance audits.
Project budget and timelines – Control the project budget, with particular attention to internal hours allocated to all activities.
Identify out-of-scope activities for change orders.
Proactively manage operational aspects of the clinical trial, including trial timelines, budget, resources and vendors. Coordinate tasks and deliverables from all functional departments involved in the project.
Communicate effectively with study team members, functional departments, and senior management.
Manage and report on recruitment status and highlight initiatives needed to meet recruitment timelines.
Project team leadership – Lead the core project team, which may include: Associate Project Managers, Project Coordinators, and Project Assistants.
Ensure all team members have adequate training on the project.
Work closely with vendors and the following internal teams to ensure all tasks and deliverables are completed on time, according to plans and according to applicable standards: Site Selection, Regulatory Affairs, Data Management, Clinical Monitoring, Biostatistics, and Scientific Affairs.
Experience
At least 6 years of industry experience, including a minimum of 3 years leading multi-center clinical trials (phase II-III)
Experience leading concurrent multi-centered clinical trials with budgets in excess of $3M USD
Experience managing dermatology trials at Project Management level
Please contact Chris Boateng at chris.boateng@arm.co.uk or apply via LinkedIn
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