Clinical Project Manager - Dermatology

Overview Life Sciences Specialist working with Pharmaceutical and Biotech companies to source the best talent across Europe

Role : Clinical Project Manager - Dermatology (MUST HAVE EXPERIENCE WITHIN DERMATOLOGY AT PROJECT MANAGEMENT LEVEL)

Location : Spain (Remote)

Salary : Up to €100,000 plus bonus

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 internal teams (Site Selection, Regulatory Affairs, Data Management, Clinical Monitoring, Biostatistics, and Scientific Affairs) to ensure all tasks and deliverables are completed on time and according to applicable standards.

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 or apply via LinkedIn.

Seniority level Mid-Senior level

Employment type Full-time

Job function Project Management, Science, and Research

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