Clinical Trial Project Planner

ICON Strategic Solutions; Canada; On-site; CAD 60,000 - 100,000; Full time

Job summary

Join a leading clinical research organization as a Clinical Trial Project Planner, where your expertise in project management and planning will drive successful outcomes. You'll collaborate with cross-functional teams to optimize schedules and resource utilization, ensuring timely delivery of critical milestones. This role offers a dynamic environment where your contributions will directly impact the efficiency of clinical trials. Enjoy a competitive salary and a range of wellness-focused benefits, all while being part of a diverse and inclusive team that values your unique skills and experiences.

Benefits

Varied annual leave

Health insurance

Retirement planning

24/7 employee assistance program

Life insurance

Country-specific benefits (childcare vouchers, gym, etc.)

Qualifications

• 3+ years of project planning and management experience, ideally in pharmaceuticals.
• Bachelor's degree required; Master's preferred with relevant experience.

Responsibilities

• Identify schedule conflicts and resource peaks for resolution.
• Monitor project activities towards milestones and support critical path analyses.

Skills

Project Planning

Risk Management

Resource Management

Critical Path Analysis

Scenario Planning

Education

Bachelor's Degree

Master's in Sciences

Tools

MS Project

Planisware

OnePager

Job description

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

What you will be doing:

1. Identify and raise schedule conflicts, risks, and resource peaks/troughs appropriately for resolution.
2. Participate and contribute to cross-functional and functional teams to discuss, review, and optimize protocol/project/program schedules and study cost estimates.
3. Contribute to the review and optimization of protocol/project/program schedules and resource management plans.
4. Monitor project activities towards milestones, anticipate variances, support critical path analyses, and collaborate with the Asset PM, Clinical Operations, and project team to identify solutions to schedule risks.
5. Perform scenario planning of project timelines across protocols and therapeutic areas to optimize resource utilization and ensure efficient milestone delivery.
6. Assist in validating resource information at the project level with the project team.

Vous possédez :

Formation :

• Diplôme de niveau baccalauréat; Maîtrise en sciences avec 3 ou 5 ans d’expérience selon le cas.

Expérience :

• Au moins 3 ans d’expérience en planification et gestion de projets, idéalement dans l’industrie pharmaceutique ou secteur similaire.

Compétences utiles :

• Certification PMP souhaitée mais non obligatoire.
• Expérience en planification réglementaire ou lancement de produits.
• Maîtrise des outils de planification (e.g., MS Project, Planisware, OnePager).

What ICON can offer you:

ICON valorise la diversité et le haut rendement. En plus d’un salaire compétitif, nous proposons des avantages axés sur le bien-être et l’équilibre vie professionnelle/vie privée, notamment :

• Congés annuels variés
• Assurances santé adaptées
• Planification de la retraite
• Programme d’aide aux employés 24/7
• Assurance vie
• Avantages spécifiques selon le pays (bons pour la garde d’enfants, gym, etc.)

Pour en savoir plus, visitez : https://careers.iconplc.com/benefits

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