⚡ New

Clinical Research Associate

Kelly Science, Engineering, Technology & Telecom

São PauloFull-timeMid LevelOn-site

Job Description

Job Title: Clinical Research Associate (CRA)

Contract: 12-Month Fixed - Brazil

Start: To be Confirmed (Pipeline Opportunity)

Organisation: Leading global life sciences company (via Kelly FSP)

Location: Brazil (Hybrid)


Job Overview:

Kelly is pipelining talent for an evergreen CRA role in pharma. If you’re looking for a project-based career as a CRA, we’d love to have a preliminary conversation, connect with us to explore future opportunities!


This is a pipeline opportunity for proactive candidates interested in joining a global leader in the life sciences industry.

The Clinical Research Associate (CRA) is responsible for overseeing clinical trials and ensuring compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements. The CRA monitors the progress of clinical studies conducted at investigative sites and ensures that data is collected, recorded, and reported accurately.


Key Responsibilities:

  • Conduct site visits (initiation, monitoring, and closeout) to ensure adherence to study protocols and regulatory requirements.
  • Verify that study data and documentation are accurate, complete, and maintained according to GCP.
  • Identify, resolve, and escalate site issues related to protocol compliance or subject safety.
  • Act as the primary liaison between the sponsor and investigative sites.
  • Review and collect essential documents for the Trial Master File.
  • Train and support site staff on study procedures and protocol requirements.
  • Ensure timely reporting of adverse events and deviations.
  • Assist in subject recruitment and retention strategies.
  • Prepare and maintain accurate monitoring reports and documentation.
  • Communicate findings and follow-up activities to stakeholders.


Qualifications:

  • Bachelor’s degree in life sciences, pharmacy, or relevant field (required).
  • Prior experience as a CRA or in clinical research (3-7 years)
  • Knowledge of Good Clinical Practice (GCP) and relevant regulatory guidelines.
  • Strong attention to detail and organizational skills.
  • Effective written and verbal communication abilities.
  • Ability to travel frequently.


Preferred Skills:

  • Familiarity with Electronic Data Capture (EDC) platforms.
  • Problem-solving and conflict resolution.
  • Ability to work independently and in a team environment.
  • 3-7 years as a CRA


Why Join?

  • Opportunity to join a globally recognised life sciences company through Kelly’s FSP model.
  • Work with international experts on high-impact projects.
  • Gain global exposure and expand your clinical knowledge.
  • Be part of a collaborative, growth-focused work culture.
  • Pipeline opportunity with anticipated hiring in the near future, apply early to be considered once the position is formally approved and released.



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