data verification

Clinical Research Associate

posted by: spj_bot

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

 

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical part in driving innovation and making an impact in the clinical research space, while enjoying a stimulating professional environment that encourages personal and intellectual growth.

 

Main Responsibilities:

  • Perform monitoring of international clinical trials across Phases I–IV, ensuring protocol adherence and data integrity at investigational sites.
  • Guarantee scientific, regulatory, and technical quality through meticulous oversight and application of GCP and local regulatory standards.
  • Manage investigational product (IP) logistics including reconciliation, storage, dispensing, and inventory, with special focus on blinded/randomized protocols.

Beyond that, you will also be able to:

Job Skills

View the job post & apply
Login/Signup

Clinical Research Associate (Closeout)

posted by: spj_bot

About the Job

Join Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.

This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will be responsible for monitoring clinical studies and ensuring compliance with regulatory requirements, while supporting investigators and site staff to ensure the safety and integrity of participants.

Main Responsibilities:

  • Perform closeout visits in accordance with study protocols and GCP guidelines.
  • Ensure timely and accurate collection of study data, including on-site source data verification.
  • Assist in the preparation of monitoring reports, ensuring compliance with internal and external standards.
  • Provide training to site staff on protocol requirements, data entry, and study procedures.
  • Communicate effectively with study teams and site personnel regarding study progress and challenges.
  • Identify and resolve issues that may impact the integrity of data or the rights and safety of participants.
  • Support the preparation for audits and inspections, maintaining compliance at the site level.

Requirements

About You:

Job Skills

View the job post & apply
Login/Signup
Subscribe to data verification

SPJ is not just a platform; it's a transformative force in the maritime sector. We reinvent job discovery and collaboration, leveraging cutting-edge AI to create a space where careers thrive and innovations set sail.

Featured Posts

Contact