Project Manager

🕒 August 10

🇺🇸 United States – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👷‍♀️ Project Manager

👻 Ghost score 35%

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Logo of Castor

Castor

201 - 500 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Castor is a modern clinical trials platform designed to facilitate research data management and patient experiences in clinical studies. It offers solutions such as Electronic Data Capture (EDC), electronic Patient Reported Outcomes (ePRO), and electronic Consent (eConsent), ensuring secure and compliant processes in line with industry standards like GDPR and HIPAA. The platform supports decentralized clinical trials (DCT) and integrates various sources to manage real-world evidence efficiently. Castor positions itself as user-friendly and supports academic, biotech, and pharmaceutical research sectors.

📋 Description

• Ensure individual study milestones are met while maintaining high data quality • Act as a bridge and consultant to customers • Drive project delivery across all phases of a study • Ensure strategic objectives are met and maximize customer satisfaction • Perform assurance activities related to the availability, integrity, and confidentiality of customer, business partner, employee, and business information • Manage a high volume of lower-complexity studies • Guide clients through complex project plans and serve as a trusted advisor • Lead solutions and apply critical thinking to project challenges • Navigate risk, identify downstream impacts, and architect solutions that safeguard project integrity • Collaborate remotely through deep work and asynchronous communication • Give and receive direct, data-driven feedback

🎯 Requirements

• 3+ years of Project Management experience in the Software Development Lifecycle (SDLC) • Understanding of EDC/CDMS, eConsent, and eCOA solutions and services • Passion for positive, customer-focused outcomes achieved with a high degree of ethics and integrity • Highly organized with strong attention to detail • Ability to plan, lead, facilitate, and document effective meetings • Collaborative and resourceful approach with a “can do” attitude and appetite to learn and grow • Understanding of ICH-GCP (Good Clinical Practice), FDA 21 CFR Part 11, and relevant GXP regulations and guidances • Solid understanding of medical terminology in the clinical trials space • Ability to understand clinical protocols and translate them into client requirements/scope • Knowledge of data management processes, including SAE reconciliation, external data vendor reconciliation, local laboratory data management, and new technology • Candidates accepted within +2/-2 CET • Applications not accepted from France, Germany, Spain, or Switzerland

🏖️ Benefits

• Remote-first work with schedule autonomy and asynchronous communication • Unlimited annual leave with a 25-day minimum • Quarterly downtime weeks for deep focus, learning, or catching up • AI tools and training • Employee Stock Option Plan (ESOP) options • Free access to Open Up for mental health • Specialized sleep courses for employees and their families • Home office budget • Guaranteed “Happy Holidays” annual bonus every December

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