P

Precision for Medicine

Global CRO for precision medicine trials

Project Support Specialist 2

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 professional level.
  • Working knowledge of ICH-GCP, Precision standard operating procedures, and regulatory guidance.
  • Ability to work and plan independently as well as in a team environment.

Responsibilities

  • Manage the meeting lifecycle by scheduling internal and external meetings, preparing and circulating agendas, taking and circulating meeting minutes, updating minutes based on team member input, and filing agendas and minutes in the Trial Master File.
  • Assist in creating and maintaining the project timeline in Microsoft Project or a similar system; collect, capture, and document team-member updates and ensure they are communicated 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 appropriate training, documenting completion in appropriate systems, maintaining training records, and filing records in the Trial Master File.
  • Review team-member training compliance periodically, identify training 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 team-member access, and ensuring prompt removal of access for team members no longer affiliated with the study.
  • Order study supplies and address queries about study supplies.
  • Prepare study binder materials and coordinate with vendors to ensure proper binder creation and shipping to study sites; obtain project-related cost estimates, verify vendor quotes against invoices for completed binders, 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 specific tasks for time tracking.
  • Review and approve weekly time reporting by team members and identify and escalate time-reporting 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 translation completeness, and managing vendor payments.
  • Support management of project-specific vendors 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, including Operations Manuals, ISFs, 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 updates, by preparing initial drafts, collecting team-member input, and finalizing content.
  • Collect data and maintain monthly key performance indicators and project health data; circulate data to the Project Manager and internal team members as appropriate.
  • Collect functional-team input for quarterly inspection-readiness reviews.
  • Support team leaders with producing study reports and updates, including country/site initiation, activation, and recruitment updates, as needed.
  • 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 for Medicine

Global CRO for precision medicine trials

Precision For Medicine is a global clinical research organization (CRO) that helps life sciences companies run clinical trials from early to regulatory approval. It specializes in precision medicine, focusing on oncology, cell and gene therapy, and rare diseases. The company combines clinical trial services with specialty laboratory work and data sciences to improve speed, reduce costs, and increase the likelihood of success in bringing therapies to patients. It differentiates itself by integrating advanced technologies and data-driven biostatistics with specialized labs to support end-to-end trials across all stages. Its goal is to enable faster, more cost-efficient development of targeted therapies that meet regulatory requirements and reach patients in need.

Company size
1,001-5,000
Company stage
Growth Equity (Venture Capital)
Total funding
$225M
Headquarters
Bethesda, MD
Founded
2012

Recently Posted Jobs

Explore more opportunities at Precision for Medicine

See more jobs