Clinical Trial Manager
Philadelphia, PA (Hybrid)
$130,000 - $160,000
Job Description
A pioneering precision medicine enterprise is actively seeking a Clinical Trial Manager to join its esteemed team. Renowned for leadership in targeted oncology, the company is dedicated to reshaping the landscape of cancer care. Utilizing state-of-the-art technologies, they tailor treatments to meet the unique needs of individual patients. Embracing a collaborative culture, the company fosters innovation, providing an opportunity for professionals to contribute to groundbreaking advancements in precision oncology. This CTM will hold a pivotal role in steering the evolution of healthcare, leaving a lasting impact on the lives of cancer patients.
Key Qualifications
- Proven track record with a significant duration of experience working specifically in the field of Oncology within the pharmaceutical or biotech industry.
- In-depth knowledge of Oncology clinical trials, including protocol design, patient recruitment, and monitoring, with a demonstrated ability to navigate the unique challenges associated with neurological disorders.
- Comprehensive understanding of regulatory requirements and guidelines, ensuring compliance with regulatory standards throughout the drug development process.
- Substantial experience in managing investigational sites, building and maintaining effective relationships, and optimizing site performance to ensure successful trial execution.
- Proficiency in overseeing data review processes, including source data verification and analysis, to ensure the accuracy and integrity of clinical trial data in the oncology therapeutic area.
Roles and Responsibilities
- Lead and oversee the planning, initiation, and execution of clinical trials, ensuring adherence to protocols, regulatory requirements, and ethical standards.
- Effectively manage relationships with investigational sites, fostering collaboration, providing support, and addressing site-specific needs to optimize site performance throughout the trial.
- Implement robust data monitoring processes, conducting regular reviews and source data verification to ensure the accuracy and integrity of data collected in clinical trials.
- Ensure all aspects of clinical trials comply with relevant regulatory requirements and guidelines, collaborating with regulatory affairs to address any compliance-related issues and facilitate successful trial outcomes.
- Proactively identify potential risks associated with Oncology trials and develop strategic plans for risk mitigation. Address and resolve issues promptly to ensure the smooth progression of the trial and meet project timelines.
Benefits
- 401(k) with percentage match
- Medical, Dental, Vision
- Performance and target based bonuses
- PTO and Holidays
