Project Support Specialist

The Project Support Specialist will serve as a member of the project team, providing cross-functional support to efficiently manage assigned clinical studies at Precision for Medicine, a Clinical Research Organization specializing in precision medicine, rare diseases, and oncology.

The position can be offered fully home-based in the following locations: Poland, Serbia, Slovakia, Hungary, or Romania.

Essential Functions:

• Creates and maintains the project timeline in MS Project or a similar system, ensuring updates are captured, documented, and distributed to study team members.
• Schedules internal and external meetings, prepares and circulates agendas, takes meeting minutes, and files meeting agendas and minutes in the Trial Master File.
• Performs various activities in the Clinical Trial Management System (CTMS), including maintaining study milestone dates, updating study contact lists, managing enrolment projections, and submitting helpdesk tickets for remediation.
• Prepares, assigns, and documents study-specific training in appropriate systems, manages training records, and identifies gaps in training to engage team members or escalate as needed.
• Establishes a study-level SharePoint site or similar shared working space, ensuring appropriate access for study teams, sponsors, and others.
• Creates project-specific email boxes and maintains access for study team members.
• Manages user access to study systems by submitting user requests to the Help Desk, reviewing team member access periodically, and documenting access reviews.
• Orders study supplies and addresses queries related to study supplies.
• Orders initial study binders, collects, collates, and prepares study binders, and ensures shipping to the proper locations through a printing vendor.
• Maintains various study trackers as directed by the Project Manager, Clinical Trial Manager, or other project leaders.
• Sends communications to study sites, investigators, and others as directed by project leadership, including SUSARs, email blasts, newsletters, and other required information.
• May support the distribution and tracking of IND Safety Reports/SUSARs/CIOMS according to study team procedures, potentially under Safety staff guidance.
• May support the translation process of site-level documents as applicable, adhering to local and regional standards.
• Acts as a point of contact for project-related requests from team members, sponsors, and third-party vendors.
• Supports the preparation, distribution, and reconciliation of study materials during applicable phases of the study (Operations Manual, ISF, patient cards, etc.).
• May support team leaders with the production of various study reports and updates (e.g., country/site initiation, activation, recruitment).
• Performs other duties as assigned by the Project Manager, Clinical Trial Manager, or other Project Leadership.