Senior Clinical Research Associate - Global Trials (Hybrid)

Psi CRO

Australia

Hybride

AUD 100 000 - 150 000

Plein temps

Il y a 9 jours

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Avantages offerts par ce poste

Hybrid work arrangement
Gym access
Wellness leave
Development opportunities
Meaningful industry impact

Résumé du poste

PSI CRO Australia is seeking a knowledgeable Senior CRA to manage the clinical aspects of global projects. You will oversee site monitoring, ensure timelines and data quality, and build strong relationships with investigators and sites across Australia. Travel readiness and on-site monitoring in Phase II/III will be required.

You will mentor Jr. CRAs, deliver training, and contribute to audits and regulatory support, while working in a hybrid arrangement with flexible in-office days.

Qualifications

  • College/University degree in Life Sciences or an equivalent combination of education, training & experience.
  • At least 4 years of independent on-site monitoring experience in Australia.
  • Experience in Phase II and/or III monitoring visits.
  • Availability to travel and work across sites.

Responsabilités

  • Training, mentoring and supervising study level responsibilities for Jr. CRAs.
  • Preparation, conduct, and reporting of selection, initiation, routine and closeout monitoring visits.
  • Delivering training of investigators, site staff and project teams.
  • Work with complex studies and perform CRF review, source document verification and query resolution.
  • Be responsible for site communication and management.
  • Be involved in site identification process and contact for investigators, vendors and support services.
  • Participate in feasibility research and prepare/present at Investigator’s Meetings.
  • Support to Regulatory Affairs and maintenance of study-specific tracking systems.

Connaissances

Mentoring & supervision
Communication
Team collaboration
Adaptability
Travel readiness

Formation

Life Sciences degree

Outils

MS Office

Description du poste

PSI CRO Australia is seeking a knowledgeable Senior CRA to manage the clinical aspects of global projects. You will oversee site monitoring, ensure timelines and data quality, and build strong relationships with investigators and sites across Australia. Travel readiness and on-site monitoring in Phase II/III will be required.

You will mentor Jr. CRAs, deliver training, and contribute to audits and regulatory support, while working in a hybrid arrangement with flexible in-office days.

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