Senior Clinical Research Associate

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Primary Location Hungary
Job ID: HU_BU_CO_CRA-0822
Job Type: Full-Time

JOB DESCRIPTION

Your main responsibilities:

  • Perform site visits and monitoring activities in accordance with protocol, SOPs, GCP/ICH;

  • Participate in study site selection, including on-site and remote (by phone) pre-study site evaluation visits and feasibility assessment activities;

  • Conduct monitoring activities, including on-site and remote monitoring visits and in-house monitoring activities between visits;

  • Assist in developing patient enrollment strategies with the project team and study sites;

  • Collaborate with and coordinate site investigators ensuring overall integrity of study and adherence to guidelines, protocol and regulations;

  • Perform and assist with project-specific administrative activities as a member of the project team.

You have:

  • Degree or postgraduate qualification in nursing, life sciences or medical sciences;

  • At least two years of clinical trials related experience (as investigator, CTA, IHCRA etc.);

  • Minimum one year of experience in oncology protocols;

  • Profound understanding of ICH GCP Compliance;

  • Ability to travel 65-75% of the month;

  • Strong oral and written communication skills in both English and local language;

  • Skills in building relationship with customer;

  • Ability to work in a team or independently if required;

  • Outstanding organizational, record retention, decision making and customer service skills.

We offer:

  • Career opportunities at local, regional and global levels;

  • Support for personal and professional development;

  • Competitive salary;

  • Annual bonuses and perks;

  • 5/2 working shift;

  • Work from home option.

If you are ready to start your journey at Cromos Pharma, please send your CV to cv@cromospharma.com.

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Cromos Pharma is an international contract research organization delivering integrated clinical research solutions that accelerate drug development.

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