Project Director (Oncology) at Allucent | Torre

Project Director (Oncology)

You'll lead global clinical trials, delivering life-changing therapies to patients through expert project oversight.
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Full-time

Legal agreement: Employment

Compensation is to be agreed upon.
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Remote (for United States residents)
Shared by
Emma of Torre.ai
7 days ago

Requirements and responsibilities


At Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Project Director (PD) to join our A-team (office-based*/remote). As a PD at Allucent, you are responsible for coordinates and oversees operational project teams, customer satisfaction and continuous improvement of processes within the Global Clinical Operations (GCO) department. This position controls and monitors the quality and full-service delivery of clinical trial Allucent customers.About this role:As a proactive project director, you will:Oversee the project and be responsible for the overall quality and management of the deliver clinical trial projects and programs. This includes overseeing the budget, reviewing and approving content and costing of proposals, problem solving with project teams, and balancing multiple competing priotities.Serve as the key contact for assigned clients on delivery of scope, customer satisfaction on services and capabilities and the assessment of client needs.Lead the project team. You will demonstrate knowledge of and insight into general business principles and practices, demonstrate a growth mindset, and support the recruitment and interviewing of new employees.RequirementsTo be successful, you will posess:Minimum Bachelor’s degree in life science, healthcare and/or business degree; Master’s degree or greater preferredMinimum 8 years of relevant work experience, specifically experience in drug development and/or clinical research; CRA experience preferred.Minimum 8 years of project management experience, specifically as a clinical project manager; managing global clinical trials requiredExtensive clinical project management experience, with at least 5 years of clinical project management experienceExpert knowledge of ICH-GCP(R3), data and patient privacy practices, and applicable (local) regulatory requirementsStrong financial acumen, administrative excellence and analytical skillsIn some cases, an equivalency—consisting of a combination of appropriate education, training, and/or directly related experience—will be considered appropriate for an individual to meet the requirements of this roleTherapeutic expertise in Oncology requiredBenefitsBenefits of working at Allucent include:Comprehensive benefits package per locationCompetitive salaries per locationDepartmental Study/Training Budget for furthering professional developmentFlexible Working hours (within reason)Opportunity for remote/hybrid* working depending on locationLeadership and mentoring opportunitiesParticipation in our Buddy Program as a new or existing employeeInternal growth opportunities and career progressionFinancially rewarding internal employee referral programDisclaimers:*Our office-based work policy encourages a dynamic work environment, prescribing a minimum of 2 days in office per week for employees within reasonable distance from one of our global offices.“The Allucent Talent Acquisition team manages the recruitment and employment process for Allucent (US) LLC and its affiliates (collectively “Allucent”). Allucent does not accept unsolicited resumes from third-party recruiters or uninvited requests for collaboration on any of our open roles. Unsolicited resumes sent to Allucent employees will not obligate Allucent to the future employment of those individuals or potential remuneration to any third-party recruitment agency. Candidates should never be submitted directly to our hiring managers, employees, or human resources.”
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