Title: Clinical Project Manager - Oncology
Location: Texas-based Candidates
Position Overview: As a Clinical Project Manager specializing in Oncology, you will play a pivotal role in overseeing the planning, implementation, and execution of clinical trials for our oncology drug development programs. You will collaborate closely with cross-functional teams to ensure the successful delivery of clinical studies while maintaining compliance with regulatory standards and timelines.
Key Responsibilities:
- Lead the planning and execution of oncology clinical trials from start-up to close-out, ensuring adherence to protocol, budget, and timelines.
- Coordinate cross-functional teams, including Clinical Operations, Data Management, Regulatory Affairs, and Medical Affairs, to drive study milestones and deliverables.
- Oversee site selection, feasibility assessments, and investigator meetings to ensure efficient study start-up.
- Manage vendor relationships and third-party vendors involved in clinical trial activities, including clinical research organizations (CROs), central laboratories, and imaging vendors.
- Monitor study progress, identify risks, and implement mitigation strategies to ensure the successful execution of clinical trials.
- Collaborate with internal stakeholders to develop study documents, including protocols, informed consent forms, and clinical study reports.
- Contribute to the development of study budgets, track project expenses, and manage financial aspects of clinical trials.
Qualifications:
- Bachelor's degree in life sciences or related field; advanced degree preferred.
- Minimum of 2 years of experience in clinical project management, with a focus on oncology drug development.
- Proven track record of successfully managing oncology clinical trials from start-up to close-out.
- Strong understanding of clinical trial operations, including site management, monitoring, and regulatory requirements.
- Excellent communication and interpersonal skills, with the ability to collaborate effectively across cross-functional teams.
- Detail-oriented with strong organizational and problem-solving abilities.
- Proficiency in project management tools and software applications.
- Experience working in a fast-paced, dynamic environment within the pharmaceutical or biotechnology industry.