Project Manager – Clinical Operations

Tech Observer; Cambridge (MA); Hybride; USD 90 000 - 130 000; Plein temps

Résumé du poste

Tech Observer in Cambridge/Boston, MA is seeking an experienced Project Manager in Clinical Operations with a strong background in Pharmaceutical Development.

This hybrid role (3 days onsite per week) focuses on planning, delivery, and cross-functional collaboration across Clinical Operations, Development, and Regulatory to translate business needs into actionable project plans.

Qualifications

• Experience in pharma/life-sciences project management.
• Understanding of Clinical Development and Clinical Operations processes.
• Excellent requirements analysis and documentation skills.
• Strong stakeholder management and communication skills.
• Experience managing complex cross-functional projects.
• Exposure to CMC regulatory processes is preferred.

Responsabilités

• Drive project planning, execution, and delivery across clinical development initiatives.
• Manage project timelines, milestones, risks, and dependencies.
• Work closely with cross-functional stakeholders across Clinical Operations, Development, Regulatory, and other teams.
• Translate business needs into actionable project plans and deliverables.

Connaissances

Business Analysis

Project Management

Clinical Operations

Documentation

Stakeholder Management

Cross-functional Projects

CMC Exposure

Description du poste

We are looking for an experienced Project Manager Clinical Operations with a strong background in Pharmaceutical Development and Clinical Operations.

Cambridge / Boston, MA | Hybrid – 3 days onsite per week

Key Responsibilities:

• Drive project planning, execution, and delivery across clinical development initiatives.
• Manage project timelines, milestones, risks, and dependencies.
• Work closely with cross-functional stakeholders across Clinical Operations, Development, Regulatory, and other teams.
• Translate business needs into actionable project plans and deliverables.

Required Skills & Experience:

• Strong experience in Business Analysis and Project Management within the pharmaceutical / life-sciences industry.
• Good understanding of Clinical Development and Clinical Operations processes.
• Excellent requirements analysis and documentation skills.
• Strong stakeholder management and communication skills.
• Experience managing complex, cross-functional projects.
• Exposure to CMC (Chemistry, Manufacturing & Controls) regulatory processes is preferred.

Engagement: 12+ months (can be extended further)