Study Coordinator (full Time)- Vaginal Microbiome Study

ISGlobal

Barcelona, Spain
Depending on c + idate's experience + isglobal sca...
On-site
Coordinate recruitment of study participants
Oversee epidemiological questionnaire administration
Manage biological sample traceability and storage
ISGlobal is seeking a full-time Study Coordinator for a vaginal microbiome study focused on women in Mozambique, with responsibilities including participant recruitment, data collection, and ethical compliance. The ideal candidate should have a university degree in Health Sciences, proven experience in clinical or epidemiological studies, and advanced proficiency in English and Spanish

Job Summary

  • The role involves leading the operational implementation of a study characterizing the vaginal microbiome in women of reproductive age and pregnant women.
  • Candidates must ensure strict traceability of biological samples and coordinate their transport for 16S rRNA gene sequencing analysis.
  • The position requires acting as the primary liaison between the research team, recruitment centers, and study participants while maintaining ethical compliance.

Matching Summary

Match Score: 85

ISGlobal is seeking a full-time Study Coordinator for a vaginal microbiome study focused on women in Mozambique, with responsibilities including participant recruitment, data collection, and ethical compliance. The ideal candidate should have a university degree in Health Sciences, proven experience in clinical or epidemiological studies, and advanced proficiency in English and Spanish.

Salary

Depending on candidate's experience and ISGlobal scales

Skills & Requirements

Must-have

  • Coordinate recruitment of study participants
  • Oversee epidemiological questionnaire administration
  • Manage biological sample traceability and storage
  • Ensure adherence to Ethics Committee protocols
  • Handle informed consent processes professionally

Nice-to-have

  • Experience with sexual and reproductive health studies
  • Previous microbiome research experience
  • Empathy when handling sensitive health topics
  • Ability to manage appointment schedules effectively

Key Requirements

  • University degree in Health Sciences (Nursing, Biology, Medicine)
  • Master's degree in Public Health or Clinical Research
  • Proven experience coordinating clinical or epidemiological studies
  • In-depth knowledge of Good Clinical Practice (GCP) guidelines
  • Experience managing electronic Case Report Forms (eCRF)

Work Rights

Not specified

Tailored Resume

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