IRT Sr Project Manager / Associate Director

Currently we have an opening for a IRT Sr Project Manager / Associate Director located in Cambridge, MA. Details for the position are as follows:

Pay Range: $73-$93/hour

Job Description:

• 12-month contract with the possibility of extending or converting to permanent based on performance and budget.
• Hybrid schedule: 2 days/week onsite in Cambridge, MA. 3 days/week remote
• The Interactive Response Technology (IRT) Project Manager [ "IRT Manager”] assumes responsibility for supporting the operational execution of the IRT system used for Phase I to IV clinical studies. The IRT is a critical system in ensuring safety of all patients taking investigational medicinal product (IMP) and if not set-up correctly, could jeopardize the usability of data obtained within the clinical studies. As an expert in IRT, the Project Manager leads the set-up and testing of the system, ensuring it meets the requirements of the clinical study protocol and that associated processes are fully compliant with GxP regulations. The Project Manager continues to assume accountability of the IRT during the system's life cycle, overseeing implementation for any required amendments.
• This will require strong collaboration from the IRT Manager to work with the following team members who sit on Clinical Trial Teams:
• the Clinical Operations Study Lead (COSL) and the Quality System & Compliance (QS&C) team members to ensure our IRT system(s) meet the protocol design and compliance requirements.
• the Investigational Supply Operations team members (ISO) to support assurance that the IRT settings allow for appropriate stock of Investigational Product (IP) for study sites to allocate Investigational Product (IP) to patients.
• the Data Management representative to support IRT integrations with the Electronic Data Capture (EDC) System.
• the Biostatistics representative to ensure the IRT system meets blinding requirements, as applicable
• Further, the IRT Project Manager is responsible for supporting the Senior Director of Clinical Operations in the build-out of this role within the Clinical Systems group. Examples may include creation of an IRT Playbook that helps study teams understand Blueprint standards for IRT technology, acting as the primary contact for the IRT vendor and seeking opportunities to improve the Sponsor-Vendor partnership, nominating and implementing process improvements in the IRT space and keeping the clinical development functions abreast of IRT industry trends and technology solutions. We are looking for an emerging or proven leader who can work independently and has the experience to help Blueprint create a seamless IRT process from vendor selection through system close-out.
• Clinical Business Operations-Clinical Systems is a business unit within the Clinical Operations Department. This role will report to the Senior Director of Clinical Operations & Head of Clinical Business Operations.

Key Tasks & Responsibilities:

• Advises on the development of the clinical study protocol with particular focus on the attributes of study drug management including comparators, medical devices, randomization and blinding in relation to IRT operational optimization.
• Acts as a core stakeholder for the selection of the IRT vendor for each project. Note: Blueprint is working with selected IRT vendors at this time, but this could change.
• Leads the IRT cross-functional efforts and is accountable for the set-up and maintenance of the IRT System for assigned studies with special attention to the proper set-up of study sites and study medication, including the correct drug dispensation according to the study protocol.
• Is responsible for reviewing IRT specifications and supports the Clinical Operations Study Lead (COSL) and ISO lead to ensure they understand the specifications.
• Reviews UAT scripts that are prepared by the Quality Systems and Compliance Team for accuracy.
• Participates and may even perform UAT for each study implementation (inclusive of amendments). Also, determines the resources needed to execute the UAT scripts and works with each study team to manage timelines and activities of the IRT UAT.
• Is available to collaborate with ISO to ensure an appropriate supply of study medication for all patients in a clinical trial by implementing optimal IRT supply strategies.
• Manages on-going IRT supplier oversight such as performance management and issue resolution.
• Helps to build IRT Standards within Blueprint so efficiencies are realized.
• Is the primary lead for QS&C for audits of IRT vendors.
• Is available to provide guidance and training to study teams, on the handling of study medication within the IRT System.
• Collaborates with ISO and the COSL in review of the pharmacy manual elements that affect the IRT system.
• Collaborates with Data Management and Biostatistics on development of IRT database for any data integrations with Electronic Data Capture (EDC) system, data stratification(s), or randomization. Ensures compliance with all relevant SOPs, GCP and ICH guidelines, and legal and ethical standards.

Qualifications:

• Bachelor's Degree or equivalent. Higher degree preferred.
• 6-8 years of experience for Sr. Manager/Minimum 8 years of experience for A.D.
• Profound knowledge in the clinical study management space
• Profound knowledge in setting up Interactive Response (IRT) Systems
• Profound knowledge in GCP and knowledge of GMP
• Excellent project management skills
• Excellent communication skills (including fluent English)
• Excellent presentation skills.