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Precision AQ

Data-driven drug access and launches

Project Support Specialist 2 - Latam

Project ManagementConfirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A four-year college degree or international equivalent, or equivalent experience, ideally in a business, scientific, or healthcare discipline.
  • At least two years of relevant experience or demonstrated competencies in the key requirements of the role.
  • Fluency in Microsoft Office programs, including Outlook, Word, Excel, and PowerPoint.
  • Ability to communicate verbally and in writing in English at a proficient, professional level.
  • Working knowledge of ICH-GCP, Precision standard operating procedures, and regulatory guidance.
  • Ability to work and plan independently and in a team environment.

Responsibilities

  • Manage the meeting lifecycle, including scheduling internal and external meetings, preparing and circulating agendas, taking meeting minutes, updating minutes based on team input, and filing agendas and minutes in the Trial Master File.
  • Assist with creating and maintaining the project timeline in Microsoft Project or a similar system; collect, document, and communicate team-member updates to the cross-functional study team.
  • Perform activities and tasks in clinical systems applicable to the role and project scope.
  • Manage study-specific training by collecting, tracking, and loading training materials; assigning team members to training; documenting completion; maintaining training records; and filing records in the Trial Master File.
  • Review team-member training compliance periodically, identify gaps, engage appropriate team members to ensure training completeness, and escalate issues to the Project Manager as needed.
  • Establish a study-level SharePoint site or similar shared workspace and ensure appropriate access for the study team, sponsors, and others.
  • Create project-specific email boxes and maintain appropriate access for study-team members.
  • Manage user access to study systems by submitting requests to the Helpdesk or similar, periodically reviewing and documenting access, and ensuring prompt removal of access for team members no longer affiliated with the study.
  • Order study supplies and address related queries.
  • Prepare study-binder materials; coordinate with vendors on binder creation and shipping to study sites; obtain project-related cost estimates; verify vendor quotes against invoices; and consult the Project Manager to approve vendor payments.
  • Maintain study trackers as directed by the Project Manager, Clinical Trial Manager, or other project leader.
  • Manage adding and removing project-team members in the finance system, including assigning team members to tasks for time tracking.
  • Review and approve weekly team-member time reports and identify and escalate concerns to the Project Manager.
  • With oversight from the Safety Lead, support distribution and tracking of IND Safety Reports, SUSARs, and CIOMS according to study-team procedures in the project plan, as applicable.
  • Manage translation of site-level documents according to local and regional standards by collecting and tracking documents, collaborating with vendors, engaging stakeholders to evaluate completeness, and handling vendor payments.
  • Support project-specific vendor management by assisting with the Vendor Management Plan, providing project training and system access to vendors, tracking vendor issues, and overseeing vendor invoicing and payments.
  • Manage preparation, distribution, and reconciliation of study materials during applicable study phases, such as the Operations Manual, ISF, and patient cards.
  • Support the Project Manager in producing study plans, reports, and updates, including project-management plans and country/site initiation, activation, and recruitment materials; prepare initial drafts, collect team input, and finalize content.
  • Collect data, maintain monthly key performance indicators and project-health data, and circulate data to the Project Manager and internal team members as appropriate.
  • Collect functional-team input for quarterly inspection-readiness reviews.
  • Support team leaders in producing study reports and updates, such as country/site initiation, activation, and recruitment materials.
  • Support the Project Manager in creating and maintaining the sponsor-facing study story board.
  • Support the Project Manager in tracking out-of-scope work and prepare materials for change-order submissions with guidance.
  • Perform other duties as assigned by the Project Manager.

About the Company

Precision AQ

Data-driven drug access and launches

Precision AQ helps pharmaceutical companies get FDA-approved medicines to patients by using data, evidence, and market insights to shape access and launches. Its services combine medical science, commercial strategy, and technology development to create new pathways for drug availability and timely delivery. The company partners with drug makers to plan launches and expansion, using analytical and creative approaches to make medicines reachable and effective in real-world settings. Unlike firms that focus only on science or marketing, Precision AQ blends data-driven insights with strategic execution across development and commercialization to accelerate patient access. The goal is to raise standards in healthcare accessibility and impact by getting the right medicines to the right patients faster.

Company size
501-1,000
Company stage
Not listed
Total funding
Not listed
Headquarters
New York City, New York
Founded
Not listed

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