Clinical Supply Strategist

hace 4 meses

Buenos Aires, Argentina Pfizer A tiempo completo

This role will be accountable for activities involved in developing and implementing mid to long term Pfizer clinical supply chain strategies and networks for the Latin America (LATAM) region. One of the main roles will be to manage clinical supply operations in Argentina, including the conduction of Import/Export and vendors’ oversight.

This a regional role with global action and will have multiple responsibilities across main Global Clinical Supply (GCS) functional lines as Clinical Supply Operations (CSO), Innovative Sciences Operations (ISO), Clinical Supply Strategy & Management (CSSM) and Clinical Research Pharmacy (CRP).

Clinical Supply Operations (CSO)

Support the clinical supply end-to-end operations for LATAM countries, especially Argentina, from packaging to delivery to patients. Main roles will include Clinical Supply Logistics aiming to drive automation and efficiency in Import/Export, transportation, and distribution networks.

Innovative Sciences Operations (ISO)

Support Global Clinical Supply regional strategic plan to R&D Clinical portfolio in alignment with Pfizer’s Corporate plans.

Support the identification of key opportunities, strategies and goals to facilitate trials conduction for clinical supplies in LATAM region.

Enable Global Clinical Supply and Pfizer partners to meet patients’ needs in the region.

The role will proactively ensure quality and compliance through risk identification and mitigation plans, strategic planning and execution, and overall design input on a program and protocol basis.

Clinical Supply Strategy & Management (CSSM)

Support clinical supply strategic plans, including product demand and customized studies designs, to ensure timely delivery and resource optimization for Clinical Trials and Early Access programs conducted in the region (e.g., Compassionate, Expanded & Post-Trial Access programs).

Clinical Research Pharmacy (CRP)

Support of Investigational Product (IP) handling activities to ensure optimal clinical trial conduct in LATAM by acting as Pfizer IP Coordinator (PIPC). Educate clinical site personnel through in-services, investigator meetings and clinical site initiations or follow-up visits on the proper handling and use of investigational products, when necessary.

Support Clinical Research Pharmacy (CRP) strategy implementation and continuity across LATAM.

MUST-HAVE QUALIFICATIONS: - B.S. degree (or equivalent) is required (Pharmacy preferred), with 1 year minimum of relevant experience (preferably in or with the pharmaceutical industries). - Previous experience with clinical supply importation process and/or commercial importation process in Argentina. - Work experience must include some of the following: drug development, clinical study design, scientific research, pharmaceutical manufacturing / packaging / labeling, cGMP requirements, leading project teams. - Ability to speak major languages (English and Spanish) in the region to communicate with local authorities & partners, and read local documents related to clinical supplies. - Great verbal and written communication skills with strong internal and external relationship skills. - Advanced Microsoft Office Suite skills and strong competency with tools.

PREFERRED QUALIFICATIONS - Clinical Research Experience (i.e., CRA/Monitoring, regulatory, clinical supply chain) preferred. - A degree in Pharmacy is preferred.

Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

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