Project Manager

🔥 0 minutes ago

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Castor

WebsiteLinkedInAll Job Openings

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 concerning the availability, integrity, and confidentiality of customer, business partner, employee, and business information • Guide clients through complex project plans • Serve as a trusted advisor and high-level consultant to clients • Navigate project risks, identify downstream impacts, and architect solutions • Plan, lead, facilitate, and document effective meetings • Collaborate remotely using deep-work and asynchronous communication practices

🎯 Requirements

• 3+ years of Project Management experience in the Software Development Lifecycle (SDLC) • Understanding of EDC/CDMS, eConsent, and eCOA solutions and services • Customer-focused approach with strong ethics and integrity • Highly organized with strong attention to detail • Ability to plan, lead, facilitate, and document effective meetings • Collaborative, resourceful, can-do attitude and appetite to learn and grow • Understanding of ICH-GCP, FDA 21 CFR Part 11, and relevant GXP Regulations and Guidances • Ability to manage a high volume of lower-complexity studies • Ability to guide clients through complex project plans • Ability to shift from process following to solution leading and apply critical thinking • Ability to remain effective amid shifting priorities, rapid change, or undefined project parameters • Ability to proactively identify risks and downstream impacts • Ability to collaborate remotely and work asynchronously • Preferred: understanding of medical terminology in the clinical trials space • Preferred: ability to understand clinical protocols and translate them into client requirements/scope • Preferred: knowledge of data management processes, including SAE reconciliation, external data vendor reconciliation, local laboratory data, and new technology • Preferred: PMP, PRINCE2, or other Project Management certification • Preferred: life science, IT, or another suitable degree • Must be able to work within +2/-2 CET • Applications are not accepted from France, Germany, Spain, or Switzerland

🏖️ Benefits

• Remote-first work with work-life integration • Flexible scheduling and asynchronous communication • Unlimited annual leave with 25-day minimum • Quarterly downtime weeks • AI tools and training • Employee Stock Option Plan (ESOP) • Free access to Open Up for mental health • Specialized sleep courses for you and your family • Home office budget • Guaranteed "Happy Holidays" bonus every December