Clinical Research Associate 18 Month Ftc - Serbian Speaking

ProPharma

Hybrid
Serbian and english language proficiency
Clinical monitoring activities
Gcp and regulatory requirements
ProPharma is seeking a Serbian-speaking Clinical Research Associate (CRA) for an 18-month fixed-term contract. The role involves clinical monitoring and ensuring compliance with protocols and regulatory requirements while fostering a collaborative work environment

Job Summary

  • The Clinical Research Associate position is responsible for clinical monitoring for assigned protocols and investigational sites, ensuring compliance with study protocols, SOPs, GCP, and regulatory requirements.
  • Main responsibilities include conducting various monitoring visits (initiation, interim, close-out), writing monitoring reports, supporting study start-up activities, and managing site personnel training.
  • ProPharma partners with clients through an advise-build-operate model across the complete product lifecycle, offering customizable consulting solutions to de-risk and accelerate drug and device programs.

Matching Summary

Match Score: 85

ProPharma is seeking a Serbian-speaking Clinical Research Associate (CRA) for an 18-month fixed-term contract. The role involves clinical monitoring and ensuring compliance with protocols and regulatory requirements while fostering a collaborative work environment.

Skills & Requirements

Must-have

  • Serbian and English language proficiency
  • Clinical monitoring activities
  • GCP and regulatory requirements
  • Electronic data capture (EDC)
  • CTMS, IVRS, and eTMF experience

Nice-to-have

  • Proactive planning and goal accomplishment
  • Problem-solving and training abilities
  • Organizational skills and attention to detail

Key Requirements

  • Over 5 years of experience as a Clinical Research Associate
  • Bachelor's degree or equivalent experience
  • Knowledge of ICH Guidelines and GCPs

Work Rights

Not specified

Tailored Resume

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