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Senior Clinical Project Manager - Dermatology

Advanced Resource Managers

Frankfurt

Remote

EUR 93.000 - 110.000

Vollzeit

Heute
Sei unter den ersten Bewerbenden

Zusammenfassung

A global CRO specializing in Dermatology is seeking a Senior Clinical Project Manager to oversee multi-center clinical trials. Candidates must have over 6 years in the industry, with at least 3 years in project management, particularly in dermatology. This role includes managing project budgets, ensuring audit readiness, and leading a project team. Remote work options are available. Competitive salary and bonuses are offered.

Qualifikationen

  • At least 6 years of experience in the clinical research industry.
  • 3+ years leading multi-center clinical trials (phase II-III).
  • Experience in managing dermatology trials.

Aufgaben

  • Oversee preparation of project deliverables like study plans and reports.
  • Ensure sites are adequately supplied for the study.
  • Manage risk and ensure audit readiness of studies.
  • Control project budget and timelines effectively.
  • Lead and train the core project team.

Kenntnisse

Clinical trial management
Team leadership
Risk management
Budget control
Regulatory knowledge
Jobbeschreibung
Overview

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

Location: Germany (Remote)

Salary: Up to €110,000 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
  • 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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