Freelance Regional Clinical Trial Coordinator

7 dni temu

zdalnie, Polska RHO Inc Pełny etat 40 000 zł - 60 000 zł rocznie

We are seeking a detail-oriented and collaborative Regional Clinical Trial Coordinator (RCTC) to support the execution of clinical trials at the site level. This role ensures operational excellence through administrative coordination, documentation oversight, and system management in compliance with ICH-GCP and local regulations.

Key Responsibilities:

  • Coordinate and support regulatory-defined trial activities and stakeholder communications.
  • Ensure timely delivery of trial materials and documentation across OPU and site levels.
  • Maintain and oversee technical systems for trial management, access control, and data completeness.
  • Support documentation processes including authoring, tracking, and translation coordination.
  • Facilitate meetings and interface management with trial teams, sites, and vendors.
  • Manage local trial supplies and ensure system accuracy and functionality.
  • Collaborate with Clinical Trial Managers and TMF teams to maintain country/site-specific records.

Requirements

Qualifications:

  • Experience in clinical trial coordination or related administrative roles.
  • Strong understanding of ICH-GCP, GDP, SOPs, and local regulatory requirements.
  • Excellent communication (including reading, verbal, and written in both local language and English) and organizational skills
  • Strong technical skills, including proficiency in Microsoft Office
  • Capabilities in managing multiple assignments and work independently

Please submit your CV/resume in English.

  • Senior Clinical Data Coordinator

    1 tydzień temu

    zdalnie, Polska Indero Pełny etat 40 000 zł - 80 000 zł rocznie

    The Senior Clinical Data Coordinator will participate in various clinical data management activities required to ensure that data captured in clinical trials undertaken, or managed by Indero, are collected, managed, and reported clearly, accurately and securely. In addition, this position is required to conduct all these activities in conformance with...

  • Clinical Operations Lead

    1 dzień temu

    zdalnie, Polska Incyte Corporation Pełny etat

    Overview:SummaryThe Clinical Operations Lead supports the Clinical Trial Manager/operational team in execution of the trial (s). The function includes direct liaison with CROs and other ancillary vendors, as appropriate, to manage relevant trial(s) operational tasks. The COL maintains effective communication with project team through oral and written...

  • Senior Clinical Data Manager

    7 dni temu

    zdalnie, Polska Indero Pełny etat 60 000 zł - 120 000 zł rocznie

    As a Senior Clinical Data Manager, you will ensure that data captured in multiple clinical trials undertaken or managed by Indero is collected, managed, and reported clearly, accurately and securely.This role will be perfect for you if:You want to work on studies end-to-end (involved from protocol review to database lock)You have the experience and...

  • Freelance Data Analyst, Poland

    3 dni temu

    zdalnie, Polska bb-8765-43b4-9ac1-7ab205575f0a Pełny etat

    Join us in redefining what it means to work for a CRO.When you work at Rho, it's more than just a job—you become part of the Rho Factor. We're a proud bunch of science nerds who love tackling big challenges together. We're not your typical CRO, and we're not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at...

  • Senior Regulatory Affairs Specialist

    5 dni temu

    zdalnie, Polska Indero Pełny etat 100 000 zł - 150 000 zł rocznie

    The Senior Regulatory Affairs Specialist will provide leadership for assigned projects regarding all regulatory activities that lead to startup of clinical trials and will oversee global/multinational complex large clinical trial submissions.This role will be responsible for sponsor-facing regulatory leadership and management of regulatory deliverables...

  • Business Development Manager

    1 tydzień temu

    zdalnie, Polska FutureMeds Pełny etat

    Your missionThis vacancy is available remotely in Spain, UK, Germany, Poland, Ukraine, Romania or Bulgaria and the applicant must have the right to work from one of these locations.FutureMeds is a research site network that supports the pharmaceutical industry through patient recruitment and retention via its network of research sites across seven countries,...

  • Start-Up, Project Manager

    7 dni temu

    zdalnie, Polska Indero Pełny etat 40 000 zł - 80 000 zł rocznie

    The Start-Up Manager is responsible for overseeing and managing the successful and timely activation of clinical trial sites across multiple countries. This role leads all start-up activities, ensures regulatory compliance, and collaborates with cross-functional teams to meet study timelines and client expectations. The ideal candidate will bring strategic...

  • Principal Biostatistician

    7 dni temu

    zdalnie, Polska Indero Pełny etat 80 000 zł - 150 000 zł rocznie

    The Principal Biostatistician will act as Lead Biostatistician on multiple phase 1 to 4 clinical trials and/or Biostatistical Oversight for programs of phase 1 to 4 clinical trials, providing input into the statistical sections of protocols (incl. sample size calculation/ validation), Risk-based Monitoring Plans, various Data Management (DM) documents, and...

  • Principal Biostatistician

    1 tydzień temu

    zdalnie, Polska Indero Pełny etat 120 000 zł - 180 000 zł rocznie

    The Principal Biostatistician will act as Lead Biostatistician on multiple phase 1 to 4 clinical trials and/or Biostatistical Oversight for programs of phase 1 to 4 clinical trials, providing input into the statistical sections of protocols (incl. sample size calculation/ validation), Risk-based Monitoring Plans, various Data Management (DM) documents, and...

  • Senior Statistical Programmer

    1 tydzień temu

    zdalnie, Polska Indero Pełny etat 60 000 zł - 120 000 zł rocznie

    The Senior Statistical Programmer will lead single and/or multiple clinical trials and be responsible for the development, maintenance, and validation of annotated Case Report Forms (aCRFs) as well as of specifications and statistical programming of Standard Data Tabulation Model (SDTM) datasets, Analysis Data Model (ADaM) datasets (or derived datasets, as...