[Hiring] Clinical Trial Project Planner @Pharmaceutical Research Associates, Inc

Pharmaceutical Research Associates, Inc; Deutschland; Remote; EUR 60.000 - 80.000; Vollzeit

Zusammenfassung

A leading clinical research organization is hiring a remote Clinical Trial Project Planner. This role involves identifying schedule conflicts, contributing to project teams, and managing timelines. Candidates should have a Bachelor's degree and at least three years of project management experience in the pharmaceutical sector. A competitive salary and various benefits are offered, and the work environment promotes inclusion and accessibility.

Leistungen

Competitive salary

Health insurance

Retirement plans

Well-being programs

Qualifikationen

• 5+ years experience with a Bachelor's or 3+ years with a Master's.
• At least 3 years in project planning and management.
• Experience in the pharmaceutical industry or similar sector.

Aufgaben

• Identify schedule conflicts and risks for resolution.
• Participate in cross-functional teams to optimize schedules.
• Monitor project activities towards milestones and mitigate risks.

Kenntnisse

Project planning

Risk management

Problem-solving

Communication

Team collaboration

Ausbildung

Bachelor’s degree or equivalent

Tools

MS Project

Planisware

OnePager

Jobbeschreibung

Aug 03, 2025 - Pharmaceutical Research Associates, Inc is hiring a remote Clinical Trial Project Planner. Location: Canada.

Overview

As a Clinical Trial Project Planner, you will join the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.

Responsibilities

What you will be doing:

• Identify and raise schedule conflicts, risks, and resource peaks/troughs for resolution.
• Participate in and contribute to cross-functional teams to discuss, review, and optimize protocol/project/program schedules and study cost estimates.
• Monitor project activities towards milestones, anticipate variances, support critical path analyses, and partner with relevant teams to mitigate schedule risks.
• Perform scenario planning of project timelines to optimize resource utilization and ensure efficient delivery.
• Validate resource information at the project level with the team.

En quoi consistera votre travail:

• Identifier et soulever les conflits de calendrier, risques et pics/creux de ressources pour résolution.
• Participer et contribuer aux équipes pour discuter, examiner et optimiser les calendriers et plans de gestion des ressources.
• Suivre l’évolution des activités du projet, anticiper les écarts, et collaborer pour identifier des solutions aux risques liés au calendrier.
• Planifier les échéances des projets pour une utilisation optimale des ressources.
• Valider les informations sur les ressources avec l’équipe du projet.

Qualifications

You are:

Education

• Bachelor’s degree or equivalent; S. with 5+ years or M.S. with 3+ years of experience.

Experience

• At least 3 years in project planning and management.
• Experience in the pharmaceutical industry or similar sector.

Beneficial Capabilities

• PMP certification (preferred but not required).
• Experience with regulatory submission planning and product launch planning.
• Proficiency with planning tools like MS Project, Planisware, OnePager.

Vous possédez:

Formation:

• Diplôme de niveau baccalauréat ou équivalent; Maîtrise en sciences avec 3-5 ans d’expérience.

Expérience:

• Au moins 3 ans dans la planification et gestion de projets.
• Expérience dans l’industrie pharmaceutique ou secteur similaire.

Compétences utiles:

• Certification PMP souhaitée mais non requise.
• Expérience en planification réglementaire ou lancement de produits.

What ICON can offer you:

Our success depends on our people. We offer a competitive salary and a range of benefits including leave entitlements, health insurance, retirement plans, and well-being programs. Visit our careers site for more info: https://careers.iconplc.com/benefits

ICON values inclusion & belonging, providing an accessible environment for all candidates. We are committed to non-discrimination and equal opportunity employment. For accommodations, contact us through the provided form.