In-house CRA

Your main responsibilities:

• Assisting CRAs in their routine work; 
• completing submission of documents to the Regulatory Authority (including safety reports) when required;  
• reporting safety data to Sponsor’s Pharmacovigilance Department and providing assistance when required; 
• performing remote monitoring and site management; 
• collecting, reviewing and tracking regulatory documents when required; 
• performing translations (only in case of appropriate education); 
• assisting with the completing of study specific documents, annotated Case Report Forms (CRFs), tracking forms, and other study
• related documents; 
• participating in study specific training;  
• providing status updates to CRAs and Project Manager; 
• participating in the preparation and coordination of investigator meetings; 

You have:

• Fluency in English and local language (written and spoken);
• higher education (a degree in science or a related field would be an asset); 
• knowledge of ICH-GCP and national regulations related to clinical trials; 
• good to excellent verbal and written communication skills; 
• computer literacy: skills of proficient work with MS Office; 
• good to excellent organizational, record retention, decision making, customer service, and interpersonal skills;  
• ability to establish and maintain effective working relationships with coworkers, managers and clients.

We offer:

• Competitive salary and benefits;
• Annual bonus scheme;
• Flexible working arrangements;
• Career opportunities at local, regional and global levels;
• Support for personal and professional development (trainings, coaching, career development, international assignments, etc).

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.