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Jobs in Munster, United States

Clinical Project Manager - Dermatology

Advanced Resource Managers

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EUR 90,000 - 100,000
21 days ago
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Clinical Project Manager - Dermatology
Advanced Resource Managers
Köln
Remote
EUR 90.000 - 100.000
Full time
21 days ago

Job summary

A leading CRO is seeking an experienced Clinical Project Manager with expertise in dermatology to oversee multi-center trials. The role includes managing project budgets, timelines, and a core project team, ensuring quality deliverables and audit-readiness. Candidates should have at least 6 years in the industry and 3 years of experience leading trials. This position offers a competitive salary of up to €100,000 plus bonuses and the flexibility of remote work.

Qualifications

  • At least 6 years of industry experience in clinical project management.
  • Minimum of 3 years leading multi-center clinical trials (phase II-III).
  • Experience managing dermatology trials at Project Management level.

Responsibilities

  • Oversee project deliverables including study plans, protocols, and reports.
  • Ensure studies are audit-ready and monitor quality of deliverables.
  • Control project budget, timelines, and resources effectively.
  • Lead the core project team and ensure adequate training on projects.
  • Communicate effectively with all stakeholders involved in the project.

Skills

Project management
Clinical trials management
Risk management
Budget control
Team leadership
Job description
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.

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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* The salary benchmark is based on the target salaries of market leaders in their relevant sectors. It is intended to serve as a guide to help Premium Members assess open positions and to help in salary negotiations. The salary benchmark is not provided directly by the company, which could be significantly higher or lower.

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