Allucent is hiring a
Associate Project Director

Summary

The job is for an Associate Project Director at Allucent™, a remote position responsible for overseeing and managing clinical trials in various therapeutic areas. The role requires strategic planning, trial management, budget and resource management, team leadership, regulatory compliance, risk management, vendor management, data management, safety monitoring, communication, quality assurance, and documentation. The candidate should have a bachelor's degree in life sciences or a related field, at least 6 years of relevant work experience, and specific skills in project management, leadership, communication, data analysis, and English language proficiency.

Requirements

• Bachelor's degree in life sciences or a related field (advanced degree preferred)
• Minimum 6 years of relevant work experience
• Minimum 6 years of experience in drug development and/or clinical research, with at least 4 years of clinical trial project management
• Strong knowledge of regulatory requirements and GCP
• Excellent project management, leadership, and communication skills
• Ability to analyze complex data and make informed decisions
• Excellent written and verbal communication, planning, critical thinking and organizational skills, including command of English language
• Representative, outgoing and client focused
• Ability to work effectively in a fast-paced challenging environment with a growing company
• Proficiency with various applications including, but not limited to, Microsoft Word, Excel, and PowerPoint required
• Strong presentation skills

Responsibilities

• Strategic Planning: Develop and implement strategic plans for Rare Diseases, Neurology, and Hematology trials
• Trial Management: Oversee the planning, execution, and monitoring of clinical trials
• Budget and Resource Management: Manage project budgets and allocate resources effectively
• Team Leadership: Lead and supervise a cross-functional team
• Regulatory Compliance: Stay up-to-date with evolving regulatory guidelines and ensure that trials are conducted in compliance with relevant regulations
• Risk Management: Identify potential risks and develop risk mitigation plans
• Vendor Management: Select, contract, and manage external vendors and partners
• Data Management: Oversee data collection, analysis, and reporting activities
• Safety Monitoring: Implement safety monitoring protocols and procedures
• Communication: Maintain effective communication with internal teams, external stakeholders, investigators, and regulatory agencies
• Quality Assurance: Implement quality control processes and continuous improvement initiatives
• Documentation: Ensure accurate and comprehensive documentation of all trial-related activities

Benefits

• Comprehensive benefits package per location
• Competitive salaries per location
• Departmental Study/Training Budget for furthering professional development
• Flexible Working hours (within reason)
• Opportunity for remote working depending on location
• Leadership and mentoring opportunities
• Participation in our Buddy Program as a new or existing employee
• Internal growth opportunities and career progression
• Financially rewarding internal employee referral program
• Access to online soft-skills and technical training via GoodHabitz and internal platforms