Clinical Research Coordinator
Há 10 horas
Job Title:
Site Support Colleague (Contract)
Location:
São Paulo, Brazil (Onsite)
Contract Length:
6 months
Workload:
0.5 FTE (part-time, approx. 2–3 days per week)
About the Role
We are working with a global leader in the life sciences sector to recruit a
Site Support Colleague
for their São Paulo operations. This part-time, 6-month contract is an excellent opportunity to gain experience in a highly regulated, clinical environment.
The role will provide
hands-on support at a local research and development site
, ensuring that clinical and operational teams have the tools, systems, and environment needed to deliver high-quality, compliant outcomes.
Key Responsibilities
- Act as a first point of contact for on-site staff, ensuring smooth day-to-day functioning of clinical systems and processes.
- Support site activities related to ongoing research and trials, addressing operational issues promptly to minimise disruption.
- Maintain accurate records of support activities to align with
Good Clinical Practice (GCP)
and internal quality standards. - Collaborate closely with site management, clinical operations, and IT to ensure seamless communication and issue resolution.
- Assist in monitoring compliance with site policies, SOPs, and regulatory requirements.
- Escalate complex technical or procedural issues to senior colleagues or global support teams when required.
What We're Looking For
- 1–3 years' experience
in a clinical research, site support, or related operational role. - CTA or Clinical Trial Coordinator background would be highly suitable for this position.
- Understanding of working within
GCP-regulated environments
is strongly preferred. - Strong problem-solving and troubleshooting skills with attention to detail.
- Excellent communication skills and a collaborative approach when working with multidisciplinary teams.
- Ability to work part-time on-site in São Paulo (approx. 2–3 days per week).
Why Join?
- Contribute to meaningful clinical research supporting global health.
- Gain valuable experience in a regulated, pharmaceutical environment.
- Flexible part-time role with exposure to cross-functional teams.
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