IRT Project Management - Contract - Cambridge MA
Are you ready to lead cutting-edge IRT projects that accelerate clinical breakthroughs in biotech?
Proclinical is seeking IRT Project Management to support the operational execution of IRT systems for clinical studies ranging from Phase I to IV.
Primary Responsibilities:
This role is critical in ensuring patient safety and data integrity by overseeing the setup, testing, and lifecycle management of the IRT system. You will play a key role in aligning the system with clinical study protocols and ensuring compliance with GxP regulations.
Skills & Requirements:
- Strong knowledge of clinical study management processes.
- Expertise in setting up and managing Interactive Response Technology (IRT) systems.
- Solid understanding of Good Clinical Practice (GCP) and familiarity with Good Manufacturing Practice (GMP).
- Excellent project management skills with a focus on detail and organization.
- Strong communication skills, including fluency in English.
- Proficient presentation skills to effectively convey information to diverse audiences.
- Bachelor's degree or equivalent; advanced degree preferred.
The IRT Project Management's responsibilities will be:
- Lead the setup and testing of IRT systems to meet clinical study protocol requirements.
- Ensure compliance with GxP regulations throughout the IRT system lifecycle.
- Oversee implementation of amendments or updates to the IRT system as needed.
- Collaborate with cross-functional teams to ensure seamless integration of the IRT system into clinical operations.
- Provide expertise and guidance on IRT-related processes to stakeholders.
- Maintain accountability for the IRT system's performance and usability during its lifecycle.
Compensation:
If you are having difficulty in applying or if you have any questions, please contact Janelle Jones at j.jones@proclinical.com
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
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