Site Coordinator

What is expected to be done?

Support all types of feasibility inquiries at the respective site;
Assist 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.
Why join Comac Medical?

Great team of knowledgeable, high-achieving and experienced professionals;
International and diverse working 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.

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