Irt Lead

4 weeks ago

Mississauga, Canada Pfizer Full time

Posting closing date: June 17th, 2024

Date de fin d’affichage : le 17 juin 2024

Status: Regular, Full-Time

Statut : Régulier, temps plein
- (Français ci-dessous)_

IRT Lead

The IRT Global Oversight Team (IGOT) is a well-established high performing team within Pfizer's Global Clinical Supply unit striving to deliver best in class Interactive Response Technology (IRT) systems providing randomization and drug management capabilities in support of Pfizer's dynamic investigational product portfolio. The patients we serve are our number one priority and IGOT aims to employ the highest quality standards across our internal and vendor IRT solutions. As part of an innovative clinical supply chain, we routinely challenge the status quo in efforts to optimize our systems and processes.

ROLE SUMMARY

The IRT Lead is a role within the Engagement function in IGOT that will serve as a strategic partner and single point of accountability to partner lines for protocol assessments, requirements elicitation, system deployments, and resupply settings guidance for Pfizer’s IRT system developed with external vendors. The implementation of this role is intended to strengthen key interfaces within assigned therapeutic areas, streamline processes and increase agility.

The IRT Lead will be assigned when it is determined that an IRT system may be needed at the draft protocol stage. He or she will perform a preliminary protocol assessment with the Supply Chain Lead (SCL), Clinical Research Pharmacist (CRP) and clinical team members (e.g., clinician, biostatistician) to determine the most effective IRT strategy for clinical customer, investigator site, Global Clinical Supply, and ultimately for the patient. The IRT Lead will present the key preliminary requirements and IRT system recommendations to the IRT Protocol Assessment Group for final determination.

He or she will work to elicit additional protocol requirements from the clinical team, then partner with the IRT vendor to ensure the IRT system is programmed according to the protocol, test scripts are complete and accurate, and execute User Acceptance Testing (UAT) in order to successfully deploy the system into production.

The IRT Lead will serve as a member of the Clinical Supply Team and as the IGOT POC throughout the life of the study. For ongoing studies, he or she will also be available for guidance on IRT resupply settings and any requisite system amendments.

The IRT Lead will also partner with IGOT management for quality investigations, CAPA commitments and continuous improvements, SOP review and revision activities, support regulatory inspections, and limited duration teams where appropriate.

ROLE RESPONSIBILITIES
- Serve as a strategic partner and POC for protocol assessment and IRT system selection for assigned studies.
- Work with the IRT vendor to elicit and document system requirements for new and amended studies in partnership with the SCL, CRP and clinical team.
- Write and execute UAT test plans where UAT is employed.
- Work with the IRT vendor to create IRT supportive documents and investigator meeting slides for clinical teams and investigator site personnel.
- Train partnering lines on the system functionality applicable to their study.
- Provide technical expertise and knowledge sharing across engagement and system design teams to ensure consistency in standards, design and strategic decision making.
- Contribute to or lead cross line initiatives and quality investigations
- Provide input into SOPs and process development and aid in quality investigations and CAPA resolution.
- Serve as the IRT representative on Clinical Supply Teams for assigned studies.
- BA/BS, in computer science, life science, or business field desired in biopharma industry.
- Minimum 5+ years of industry experience with IRT, clinical supply and/or business analysis desired.
- Understanding of the nature of clinical data and concepts of IRT study configuration, resupply settings, blinding, privacy protection, and data quality/integrity standards
- Exposure to working in a GMP / GCP environment and with regulatory audit teams
- Project management and/or continuous improvement experience a plus
- Possess excellent English language written and verbal communication, interpersonal, collaboration and business partnership capabilities required
- Comfortable working with a global team, partners and customers in a change agile environment

PHYSICAL/MENTAL REQUIREMENTS
- Database query, business analysis and technical writing skills a plus
- Experienceparticipating in root cause analysis using tools such as FMEA, 5-Why, Cause & Effect Matrix and/or Fish Bone diagram desired
- Experience with business analysis and/or project management tools a plus (ex. MS Project, MS Visio, HP Quality Center, or any other requirements visualization and analysis tools)

We are proud to offer employees a flexible working model that is grounded on empowering colleagues to design their workdays so that t

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