Senior Manager/Associate Director, Project Management, Development

Description

Please make an application promptly if you are a good match for this role due to high levels of interest.

Why join Cardurion Pharma?

At Cardurion, we are advancing the understanding of signaling pathways that regulate heart cell function. Our programs seek to modulate these pathways to reverse the pathophysiological mechanisms that drive cardiovascular disease. We invite you to explore our website to learn more about our Company and how we are advancing our drug candidates to improve health outcomes and impact lives around the world.

The Role

The Senior Manager / Associate Director will play a pivotal role in supporting our drug development programs from preclinical stages through clinical trials. This position requires a flexible and perceptive problem solver, with a strong background in pharmaceutical development, project management, and cross-functional collaboration. The ideal candidate will assist a development team and work closely with internal and external stakeholders to ensure the successful progression of drug candidates. The individual will be supporting the Program Manager for one of Cardurion’s clinical assets and would be responsible for ensuring consistency and quality of the overall trial / program communications, direction implementation, coordination, execution, control, monitoring, and maintaining the integrated development plan and completion of cross-functional projects. The position works closely with all functional team development teams (e.g., Clinical, Operations, CMC, Regulatory, and all contributing partners).

This position reports to the Director of Project Management. We’d prefer this position to be hybrid based at our headquarters in Burlington, MA but will consider remote candidates.

Here’s What You’ll Do

• Key member of the Global Program Team driving cross-functional strategy and plans while creating a collaborative culture.
• Effective communication with all members of the Global Program team and Leadership.
• Collaborate with the Program Manager to track program progress, develop integrated development plans, identify risks, and implement mitigation strategies to ensure successful project delivery.
• Work with sub-teams and cross-functional team members to monitor, track, and evaluate the progress of the integrated development plan, identifying and logging risks and supporting the implementation mitigation strategies.
• Collaborates with the cross-functional team to ensure program budget and forecasts are maintained and updated with all cross-functional team members.
• Assist and manage drug development projects, ensuring alignment with corporate strategy and timelines.
• Support the planning and tracking of preclinical and clinical studies, including study design, protocol development, and regulatory submissions.
• Provide planning input during project meetings, maintaining clear communication with stakeholders.
• Collaborate and share expertise with team members, fostering a culture of innovation and continuous improvement.
• Maintain high-quality Project Management Standards and Deliverables.
• Knowledge of Project Management related and Microsoft Office Software Programs.

Here’s What We’ll Bring To The Table

Our Mission :

Translate our world-class expertise in cardiovascular signaling pathways into groundbreaking therapeutics for patients.

Cardurion is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person’s race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation, or any characteristic protected under applicable law. Cardurion will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.

Requirements

Here’s What You’ll Bring to the Table :

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