Project Manager

Incendia Therapeutics Inc - Cambridge, MA

Full-time - Mid Level

Cambridge, MA

About the position

Incendia Therapeutics is seeking a dynamic and experienced Project Manager to join our early-stage biotechnology company. This role is critical to advancing our innovative pipeline and supporting our mission to provide novel therapeutics for cancer patients in need. The Project Manager will manage clinical and non-clinical projects, ensuring alignment with business goals, overseeing trial progress, and coordinating with CROs and internal teams.

Responsibilities

• Manage multiple aspects of our clinical development program, ensuring alignment with overall business objectives and timelines.
• Oversee the progress of clinical trials from early-stage through late-stage.
• Develop and maintain detailed project plans, including timelines, milestones, and resource allocation.
• Facilitate meetings with internal teams, external partners, and Contract Research Organizations (CROs) to track progress, resolve issues, and ensure successful project execution.
• Manage relationships with CROs, ensuring high-quality performance and adherence to project timelines and budgets.
• Oversee operational aspects of both non-clinical activities and clinical trial activities, including CRO selection and non-clinical study management, site selection, patient recruitment, and data management.
• Coordinate with cross-functional teams to integrate non-clinical, clinical, regulatory, and quality activities across all stages of development.
• Prepare project updates and dashboards, articulating project progress and challenges.
• Monitor and manage the company's pre-development projects.
• Work with teams to track progress, identify risks, and implement mitigation strategies.
• Ensure clear and effective flow of information between functions.
• Provide input on resource allocation to align with company goals and objectives.

Requirements

• Bachelor's degree in Life Sciences, or a related field; advanced degree preferred.
• Minimum of 6 years of project management experience in the biotech or pharmaceutical industry, with a proven track record in managing clinical and non-clinical projects.
• Strong understanding of clinical trial processes, regulatory requirements, and CRO management.
• Excellent organizational, leadership, and communication skills.
• Ability to work collaboratively in a fast-paced, dynamic environment.
• Proficiency in project management tools and software.
• Demonstrated ability to manage multiple projects simultaneously and to adapt to changing priorities.

Benefits

• Competitive salary and benefits package.
• Opportunity for professional development and career advancement.
• A supportive and innovative work environment.
• Access to cutting-edge technology and research tools.