Parexel

Sponsor pentru viza H1B Asistență medicală Consultanță Logistică

Parexel este o organizație globală de cercetare clinică ce deservește companii biofarmaceutice pe parcursul dezvoltării de medicamente noi. Activitatea sa acoperă studii clinice de fază I–IV, gestionarea portofoliilor și a studiilor, strategia de reglementare, accesul la piață și planificarea ciclului de viață. Cu peste 21.000 de profesioniști, Parexel îmbină expertiza clinică, de reglementare și terapeutică cu perspectivele pacienților și designuri inovatoare ale studiilor. Compania sprijină cercetarea în domenii precum oncologia, neuroștiințele și bolile rare, punând accent pe eficientizarea dezvoltării clinice și pe orientarea acesteia către pacienți.

Locurile de muncă ale companiei

Senior Clinical Trial Associate – Poland (Remote)

Support global clinical study teams at Parexel across trial operations, documentation, submissions, supplies, meetings, and Trial Master File maintenance. Coordinate study information and communications across affiliates, vendors, and internal stakeholders.

acum 1 săptămână

Polonia

România

Serbia

110.000 zł – 120.000 zł / an

Remote Normă întreagă Senior Limbă Obligatorie: engleză Limbă Obligatorie: poloneză Asociat pentru studii clinice General

Google Cloud Platform

Descriere

Provide logistical support to global study management teams throughout clinical study delivery
Build and maintain working relationships with study teams, affiliates, and vendors
Support the Clinical Trial Manager with communications between study teams and affiliates
Coordinate global study supplies through designated systems
Organize study meetings and prepare presentation materials
Consolidate study data for trackers and databases
Assist with protocol feasibility, country selection, and site selection activities
Support technical and logistical study operations
Maintain study documentation and report progress
Keep study management data, contact records, country contacts, and distribution lists current
Track Health Authority, IRB, and IEC submissions and approvals in CTMS, escalating delays and issues
Provide submission and supplementary materials to affiliates or Product Development Regulatory
Maintain study-level Trial Master File completeness under Clinical Trial Manager direction
Contribute to best practices and process improvements
Apply insights and recommendations from study debriefs and established best practices

Cerințe

At least three years of global clinical-trial experience as a project specialist
Proficiency with CTMS, EDMS, Excel, Word, and related computer tools
Working knowledge of ICH-GCP Guidelines, international and local regulations, Parexel procedures, and client-specific procedures
Strong written and verbal communication skills
Ability to manage competing priorities and meet project timelines
Effective problem-solving capabilities
Ability to mentor and train less experienced colleagues when appropriate
Ability to serve actively as a process or platform Subject Matter Expert with minimal line-manager oversight
Fluency in written and spoken English and Polish
Relevant qualification or equivalent professional experience
High school diploma required; a life-science or related degree is preferred

Beneficii

Premium salary
Attractive benefits package
Medical care plan covering health, dental, and vision
Life assurance
Positive work environment
Team-oriented and collaborative culture
Access to innovative technology
Comprehensive training
Annual performance-based bonus plan for eligible roles
Annual salary review for eligible roles
Total rewards incentives for eligible roles

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Senior Clinical Trial Associate – Poland (Remote)

Support global clinical study teams at Parexel across trial operations, documentation, submissions, supplies, meetings, and Trial Master File maintenance. Coordinate study information and communications across affiliates, vendors, and internal stakeholders.

Descriere

Cerințe

Beneficii

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