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Precision Medicine GroupProject Director
Precision Medicine Group is hiring a full-time Project Director to oversee oncology clinical trials and help advance the development of novel compounds. Operating remotely from the…
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About This Role
Precision Medicine Group is hiring a full-time Project Director to oversee oncology clinical trials and help advance the development of novel compounds. Operating remotely from the UK, Spain, Poland, Hungary, Romania, Serbia, or Slovakia, this role suits experienced clinical research professionals who take a consultative approach to trial management and client partnership. The Project Director serves as a key representative on the project management career path, frequently managing global or…
Job Description
Precision Medicine Group is hiring a full-time Project Director to oversee oncology clinical trials and help advance the development of novel compounds. Operating remotely from the UK, Spain, Poland, Hungary, Romania, Serbia, or Slovakia, this role suits experienced clinical research professionals who take a consultative approach to trial management and client partnership.
The Project Director serves as a key representative on the project management career path, frequently managing global or large study portfolios and acting as a primary liaison for clients. Responsibilities include directing project managers, managing budgets and financial health, maintaining quality and inspection readiness, driving change orders, and leading cross-functional teams. This position also involves supporting senior leadership with process improvements, contributing to business development, and mentoring junior project management staff.
Precision Medicine Group operates as a people-focused contract research organization combining clinical trial designs, biomarker and data analytics solutions, and operations focused on oncology and rare diseases. The organization offers a collaborative work environment that emphasizes work-life balance and team development.
Responsibilities
- Serve as the primary point of contact and liaison for clients to deliver customer service and participate in proposals and presentations
- Oversee all aspects of clinical research trials to guarantee consistency across assigned portfolios
- Direct assigned project managers through project setup, planning, initiation, procurement, execution, and closure
- Manage study budgets and financial health to keep projects within scope, maintain profitability, and handle billable hours
- Drive change orders and ensure all functional areas understand and manage study scope
- Develop and oversee comprehensive project plans with timelines, risk management, and mitigation strategies
- Ensure quality management, eTMF inspection readiness, and implementation of corrective action plans
- Establish tracking metrics and prepare status updates for senior management and clients
- Lead internal and client meetings, set team expectations, and drive program strategies
- Communicate protocol issues and deviations to sponsors and management while implementing necessary actions
- Support business development, marketing activities, and bid defense preparation including travel as needed
- Mentor associate project managers and project managers while providing ongoing feedback and annual reviews
Requirements
- Minimum of 8 years of clinical research experience or proven competencies for the role
- Minimum of 5 years of direct project management experience
- Experience managing clinical studies within Oncology
- High proficiency with Microsoft Office Products, Microsoft Project, eTMF, EDC, and CTMS
- Expertise in pharmaceutical and/or device research
- Mastery knowledge of ICH-GCP and relevant company standard operating procedures
- Ability to travel domestically and internationally including overnight stays
- Legal authorization to work in the country of employment without employer sponsorship
Qualifications
- Bachelor’s degree or equivalent combination of education and experience in a science or health-related field for North American applicants, or a general degree or equivalent for EU applicants
- Advanced degree in a science or health-related field
- Experience managing studies within RadioPharm
Core Skills
Frequently Asked Questions
Answers are based only on the employer’s listing; where it doesn’t say, neither do we.
Is this position remote?
Yes, this role is offered fully remote from the UK, Spain, Poland, Hungary, Romania, Serbia, or Slovakia.
What is the employment type?
The position is full-time.
What experience is required for this role?
Candidates must have a minimum of 8 years of clinical research experience, including at least 5 years of direct project management experience with studies in Oncology.
What salary does this position offer?
The salary is not specified in the job posting.
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