Primary Location Hungary
Job ID: HU_BU_CO_CRA-0822
Job Type: Full-Time
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.
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.
Career opportunities at local, regional and global levels;
Support for personal and professional development;
Annual bonuses and perks;
5/2 working shift;
Work from home option.
Cromos Pharma is an international contract research organization delivering integrated clinical research solutions that accelerate drug development.