Cromos Pharma is premier Irish-based regional Contract Research Organization (CRO) providing full service in
clinical trials in Central and Eastern Europe, CIS and the USA. Our team of clinical trial professionals
contributes to improvement of people's health by translating breakthrough scientific discoveries into innovative medical treatments.
To our clients Cromos means quality, commitment and cooperation.
To our team Cromos is career, competence and creativity.
We are where the patients are.
We are looking for a talented Global Project Manager to become part of our team.
Your main responsibilities:
Management of global international multicenter clinical trials;
Be a main contact for a Client in an assigned project;
Presenting the company to Sponsors, including preparation and attending at Bid Defense meetings;
Management of CRAs and in house CRAs (IHCRAs) in frames of the clinical trial project;
Acting as the main contact for cross-departmental requests ;
Developing the Project Management Plans as per the needs of a business;
Reviewing and adapting study documents to country-specific requirements;
Maintaining the country-specific project files;
Completing and maintaining internal study metrics for the whole study and for CRAs and IHCRAs involved to a project (e.g. Operational/Financial Status Reports and other project specific tools);
To work with Clinical Trial Management System or other project related tracking tools;
Reporting to the Financial department services performed (for invoicing purposes);
Ensuring correct documentation and reporting to the Financial Department of project-related pass-through expenses;
Coordinating and controlling project team work, checking and coaching CRA, including Co-Monitoring Visits;
Assisting in audits/inspections and management of CAPAs on the project level;
To perform Vendor Management in Western/Central/Eastern Europe and Asia region (if required).
Degree or postgraduate qualification in nursing, life sciences or medical sciences;
At least 4-5 years of clinical trials related experience as PM, SPM, CPM;
At least 2-3 years of clinical monitoring experience;
Knowledge of ICH-GCP and national regulations related to clinical trials;
Excellent command of written and spoken English language;
Excellent verbal and written communication skills;
Computer literacy: skills of work with MS Office;
Excellent organizational, record retention, decision making, customer service, and interpersonal skills;
Ability to establish and meet priorities, deadlines, and objectives;
Readiness to undertake extensive business trave;
Focus on quality, precision, and punctual delivery of results;
Ability to be assertive and work independently without direct supervision as well as in a team environment.
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.
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