Use Your Power for Purpose

Our mission is straightforward: empower healthcare decisions regarding the safe and appropriate use of medicines for patients. Whether you are developing the framework to ensure our evidence is scientifically robust, providing unbiased and medically essential expertise, or exploring ways to bridge data gaps, your role is vital. By ensuring our evidence is sound and offering necessary medical insights, we strive to improve patient care and treatment efficacy.

What You Will Achieve

In this role, you will:

Coordinate and support all activities related to clinical trials, assisting managers in their execution.Assist in site activation activities, including gathering necessary documentation.Review data for quality and completeness, ensuring timely submission to data management and supporting patient safety and eligibility.Coordinate with sites to finalize budget worksheets and contractual agreements, maintaining accurate site-level information on the clinical trials registry.Support the study team with regulatory submissions, maintain the Electronic Library and Records Archive, and attend investigator meetings as required.

Here Is What You Need (Minimum Requirements)

BA/BS with at least 2 years of experience or MBA/MS with any years of experienceDemonstrated success in prior roles, including within matrix organizationsDeep understanding of quality and regulatory requirements across various countriesKnowledge of International Conference on Harmonization Good Clinical Practices and local regulationsProficiency in applications used in clinical trialsSOP compliance knowledge and expertise on all relevant SOPsEffective verbal and written communication skills, and fluency in English

Bonus Points If You Have (Preferred Requirements)

A Master's degree combined with relevant therapeutic area experienceHigh level of project management skillsStrong analytical and problem-solving skillsAbility to work independently and as part of a teamExcellent organizational and time management skillsStrong attention to detailProficiency in Microsoft SharePoint and SharePoint DesignerAbility to adapt to changing priorities and work in a fast-paced environment

  
 

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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