Project Director – Oncology

This is a fully remote position, open to applicants in United States.

📋 Description

• Act as the main point-of-contact liaison with clients, engaging in proposal activities and delivering client presentations.

• Supervise all components of clinical research trials and the assigned portfolios.

• Guide project managers through the phases of project establishment, planning, initiation, procurement, execution, and closure.

• Oversee study budgets, scope, change orders, and ensure financial health.

• Create or manage comprehensive project plans, timelines, and risk management strategies.

• Ensure quality management, eTMF inspection readiness, and the formulation of corrective/preventive action plans.

• Set up tracking metrics and monitor the progress of trials and teams.

• Prepare project status updates, KPI reports, and presentations for clients and senior management.

• Facilitate internal and client meetings while driving program or study-level strategies.

• Manage cross-functional project teams and the execution of trials.

• Communicate protocol/study-related issues and take necessary actions.

• Deliver formal presentations, including bid defenses.

• Ensure compliance and provide study-specific training.

• Assist in business development and marketing efforts, including preparation for bid defenses and travel.

• Mentor associate, project, and senior project managers.

• Engage in departmental updates and contribute to the development of company SOPs.

• Offer continuous feedback and conduct annual performance reviews for team members.

• Identify performance issues at the project level and ensure corrective measures are implemented.

• Complete required organizational training, time reporting, and administrative tasks.

• Travel domestically and internationally as needed.

⛳️ Requirements

• Bachelor’s degree or an equivalent combination of education and experience in a science or health-related field (North America).

• At least 8 years of clinical research experience or demonstrated competencies for this role.

• Minimum of 5 years of direct project management experience.

• High proficiency in Microsoft Office Suite (Outlook, Word, Excel, PowerPoint), Microsoft Project, eTMF, EDC, and CTMS.

• Experience in managing highly complex and global studies or a portfolio of studies.

• In-depth knowledge of ICH-GCP and the relevant Precision SOPs.

• Extensive experience in pharmaceutical and/or device research.

• Willingness to travel domestically and internationally, including overnight stays.

• Candidates must possess legal authorization to work in the country of employment without employer sponsorship.

🏝️ Benefits

• Discretionary annual bonus.

• Health insurance.

• Retirement savings benefits.

• Life insurance.

• Disability benefits.

• Parental leave.

• Paid time off for sick leave and vacation.