Weston - Project Manager

Company Overview:

Join our team of groundbreaking scientists and leaders today to change the world tomorrow.

External Description:

The successful candidate will be responsible for planning, executing, and monitoring drug development projects to ensure alignment with company goals and regulatory requirements.

Key Responsibilities:

1. Project Planning & Management

• Develop project plans, including timelines, milestones, and resource allocation for drug development projects.
• Monitor project progress and adjust timelines as necessary to keep projects on track.
• Identify potential project risks and develop mitigation strategies to minimize their impact.
• Coordinate with contract research organizations (CROs and CDMOs) to manage cost and timelines, ensuring timely and quality delivery of goods and services.
• Assist in budget and resource planning, working closely with the finance team to track and manage project budgets.
• Collaborate with functional heads to allocate resources, including personnel, equipment, and funding, to support project activities.

1. Scientific Coordination

• Support project teams with technical understanding of infectious disease and biologics development.
• Stay updated with relevant scientific literature to align project goals with industry advancements.
• Work with the regulatory team in preparing documents and data for regulatory submissions.
• Ensure project activities adhere to quality assurance standards and regulatory requirements.

1. Cross-Functional Team Leadership

• Facilitate communication and collaboration among cross-functional teams, including scientists, clinical, regulatory, and external consultants.
• Prepare and deliver project updates and reports to executive teams and key stakeholders.
• Escalate challenges and risks as needed, ensuring appropriate support for resolution.

Qualifications:

• 2-5+ years of project management experience in a biotech or pharmaceutical environment, preferably in drug development.
• Knowledge of biopharmaceutical drug development processes, including preclinical research, regulatory requirements, and clinical development.
• Experience contributing to IND submissions is a plus.
• Preferred: MS in a relevant scientific discipline (e.g., biology, pharmacology, immunology, biochemistry, etc.).
• Strong communication and interpersonal skills to facilitate collaboration across teams.
• Proficiency in project management tools and presentation software.
• Experience managing government-sponsored projects is a plus.
• Budget management and resource allocation experience preferred.
• PMP or other project management certification is desirable.

ModeX Therapeutics is an Equal Opportunity Employer