• Design, initiate and execute ex‐US and global clinical development strategies, plans and trials.• Support global clinical trials for specific medical questions and issues• Possess and maintain up‐to‐date expertise in GCP compliant, clinical trial design andexecution• Provide clarifications on medical items within the clinical trials

• Partnership with Medical Community;• Scientific exchange;• Clinical trials support;• Responses to unsolicited requests for information from company and other customers;• Support pre-launch and post-launch process;• Internal Interactions and support.

• Managing of clinical trials phases I-IV;• Studies preparation: feasibility research and analysis, documents and systems preparation and creation, trainings performing for all the members of study team and involved departments, study budget planning, communication with Sponsors;• Studies conduction: monitoring supervision (reports review, co-monitoring visits, compliance with GCP, SOPs and work instruction checking), refreshing trainings conduction, ensure in appropriate safety reporting, milestones achievement, budget updates and maintenance, support of interaction between departments, regular teleconferences with Sponsors;• Studies close-out: keep the timelines for data clarification and database cleaning, supervision on close-out activities, clinical report writing assistance, compliance with all the predefined timelines;• Bid defences participation;• External and internal audits preparation, participation and follow-up;• KOL interactions.

• Maintenance of the clinical trials phases I-IV;• Feasibility research, site qualification, initiation, routine monitoring and close-out visits performing;• External (Sponsor and third-side) and internal (co-monitoring and independed QA visits) audits participation;• Trainings preparation;• Investigator meetings coordination;• ICH GCP compliance checking on sites;• Managing of subjects recruitment;• Supervision on entry level CRAs;• Co-monitoring visits conduction within the mentor role;• Pharmacovigilance.

• Start of CRA responsibilities performing;• Trainings participation;• Support of clinical trials from initiation to closure stages;• Participation in clinical trials phases II-III;• Performing of all the types of monitoring visits to sites.

• Screening, diagnosing, treatment and follow-up of the patients with different cancer indications;• Non-cancerous breast conditions treatment.• Palliative therapy;• Minor surgery in primary care;• The primary and secondary prevention of Breast cancer.

• Set-up and improving of oncologist responsibilities on the basis of General oncology and Oncourology department under the supervision;• Extensive clinical work;• Intensive surgical activity;• Local and systemic chemotherapy prescription;• Scientific activity;• Familirization with clinical trials as a sub-investigator.