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Job description

Currently we are looking for a professional to coordinate clinical research studies activities, streamline processes, administration and communication between teams involved.

What is expected to be done?

• Support all types of feasibility inquiries at the respective site;
• Asist the site team with regards to subject pre-selection and recruitment;
• Help the site team in subjects’ visits planning and preparation;
• Organize various source of documentation;
• Complete Case Report Form and maintain Investigator Site File;
• Participate and coordinate any trainings and meetings (incl. Investigator Meetings) related to a specific study;
• Collaborate with the site team for any adverse events and safety information reporting and escalation;
• Organize and coordinate logistic of study medication, other study supplies and biological samples;
• Ensure timely site equipment maintenance and calibration;
• Handle subject expenses reimbursement;
• Support project team in the collection of site-specific documents;
• Support the site team in audit/inspection preparation, as needed.

Requirements

• Graduate or postgraduate degree, preferably in the filed of Biology, Pharmacy, Chemistry or other relevant;
• One year of experience in the leading role in a clinical research filed;
• Very good knowledge of clinical research process;
• Sound knowledge of current ICH/GCP guidelines and country-specific regulations;
• Particularly good organizational and coordination skills;
• Excellent communication skills both written and spoken;
• Working knowledge of Word, Excel, and Power Point;
• Fluency in English language.

We offer

• Great team of knowledgeable, high-achieving and experienced professionals;
• International and diverse work atmosphere;
• Challenging projects in a different therapeutical area as well as in early phases;
• Opportunity to enrich professional skills and progress in career development;
• Competitive salary and social benefits.