Clinical Research Professional

5 days ago


Fatih, Istanbul, Turkey Ascot Science Full time

Discover a career that truly makes a difference

A clinical research associate (CRA) plays a vital role in ensuring the integrity and quality of clinical trials. At Ascot Science, we are seeking an experienced CRA to join our team.

Job Overview

As a CRA, you will be responsible for monitoring and managing clinical trials to test the safety and efficacy of new drugs and treatments. You will work closely with site staff, including investigators, coordinators, and physicians, to ensure compliance with study protocols and regulations.

Clinical trials involve multiple stages, including recruitment, enrollment, and data collection. As a CRA, you will be responsible for verifying data accuracy, conducting site visits, and reporting any deviations or issues.

To succeed in this role, you must have excellent communication and interpersonal skills, as well as the ability to work independently and as part of a team.

Key Responsibilities
  1. Conduct qualification, initiation, monitoring, and closeout visits at research sites;
  2. Communicate with site staff to ensure compliance with study protocols and regulations;
  3. Verify data accuracy and report any deviations or issues;
  4. Support preparation of regulatory submissions when requested;
  5. Investigational product/drug accountability and inventory;
  6. Assess the clinical research site's patient recruitment and retention success and offer suggestions for improvement;
  7. Complete monitoring reports and follow-up letters;
Requirements
  • Bachelor's degree in health sciences, medical science, or a related field;
  • Four years of experience in clinical trials, with at least two years in monitoring;
  • Ability to communicate effectively in English;
  • Ability and willingness to travel;
  • Proficiency in project management tools and techniques;


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