Senior Clinical Research Associate

New
P
Precision for MedicineClinical Trial Services
SerbiaFull-TimeSenior
Salary not disclosed
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Job Details

Languages
Serbian, English, Bulgarian
Experience
3+ years of CRA experience within the CRO or pharmaceutical industry

Requirements

  • 4-year college degree or equivalent experience.
  • 3+ years of CRA experience within the CRO or pharmaceutical industry.
  • Fluency in Serbian, English, and Bulgarian languages.
  • Availability for domestic travel including overnight stays (50-60% travel commitment).
  • Experience in biopharma or relevant therapeutics areas.
  • Understanding of clinical trial monitoring and site management.
  • Strong communication and conflict resolution skills.
  • Ability to identify potential study risks and propose mitigation solutions.
  • Graduate or postgraduate degree in a scientific or healthcare discipline (preferred).
  • Experience with study start-up activities (preferred).
  • Experience with Phase I studies (preferred).
  • Understanding of financial management (preferred).

Responsibilities

  • Monitor and own the progress of clinical studies at investigative sites to ensure compliance with protocol, SOPs, ICH-GCP, and regulations.
  • Coordinate all necessary activities required to set up and monitor a study, including identifying investigators and preparing regulatory submissions.
  • Conduct pre-study and initiation visits.
  • Support Project Managers with large-scale trials.
  • Train and mentor junior staff members.
  • Interact directly with clients, initiate payments, and participate in proposal activities and client presentations.
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