Biotechnology

Job Title: Project Management Specialist

The PM will be responsible for supporting the core pillars of project management as follows:

Project Coordination & Timeline Management

Establish and track project timelines for various initiatives, ensuring all milestones are clearly defined and achieved.

QA/RA (Quality Assurance / Regulatory Affairs)

R&D; / Manufacturing (Research & Development / Manufacturing)

Clinical (Clinical Operations)

Planning & Resource Management

Support the planning process by assisting in the assessment and allocation of required resources.

Monitor and track the availability and utilization of key project resources, including:

Financial resources and budgets

Accelerate project progress by identifying bottlenecks and streamlining processes.

Proactively identify potential project risks and support the development of effective mitigation plans.

Experience:



0–10 years of proven experience in a project support role, PMO setting, or a relevant functional area.

Master’s/ Bachelor’s degree Science field.

Key Qualities:

Clinical, R&D;).

Technical Skills: Proficiency in project management tools (e.g., MS Project, Excel dashboards) and the Microsoft Office Suite (Excel, PowerPoint).

Preference- PMP certified candidates- BioPharma / Biotech industries

At Micro Crispr, you’ll be part of an innovative biotech environment where collaboration and scientific excellence drive progress.

This pivotal role offers significant exposure to the entire project lifecycle and an excellent opportunity to advance your career in project and portfolio management.

You will play a key part in driving organizational efficiency and ensuring the successful delivery of projects.

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