Senior Clinical Research Associate

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.

We provide equal opportunity to all qualified applicants and employees by prohibiting discrimination in employment decisions because of race, color, religion, sex, national origin, age, veteran status or disability.

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