Received and addresses various unsolicited medical requests from HCP sites. Planned and conducted safety assessments in close collaboration with Pharmacovigilance department. Served as a local medical TA expert and key contact for investigator sites and CRO staff. Led development and maintenance of relationships amongst HCPs. Liaised with IRBs and health authorities to streamline routine clinical operations; Responsible for training and development of junior staff and CRA teams;

Regional Associate Medical Director/ Lead CTL /Clinical Trial Liaison / Oversight CRA acting as field-based member of Medical/Clinical Ops team. Developed new and fostered existing HCP/KOL/PAG relations, representing the Company, its’ Brand and Values at the regional level in EMEA region Conducted Regeneron sponsored clinical trials support in the challenging and highly competitive trial landscape of Oncology, Cardio, Ophthalmology, Rheumatology and Rare diseases.Acted as Company Regional Oversight representative, performed oversight, enrollment booster, pre-study evaluation, Site Initiation visits. Maintained excellent communication between internal and external stakeholders, fostering matrix collaboration between departments to support strategic decision-making. Performed and reviewed study feasibility assessments using regional intelligence and previous experience. Developed creative innovative recruitment/retention strategies on a global and region-specific scale, including establishing referral site networks and cultivating patient connections. Provided strategic advice to internal clinical operations teams and senior project stakeholders on regional peculiarities and local intelligence. Reviewed and analyzed SAE/AESIs for assigned studies, developed narratives, and presented at DSMBs. Conducted TA on-boarding and ongoing trainings for new CTLs/CRO teams, educating and guiding clinical investigators and direct reports worldwide. Empowered the global CTL team, motivating to exceed expectations and outperform in an extremely competitive concurrent trials landscape. Developed presentation materials for scientific exchange, conferences and other medical education activities.Supported seamless study set up, maintenance and close out of assigned programs in EMEA countries;

Regional project management with line management function for the assigned personnel; Act as Lead CRA/Associate PM in the region for a protocol/project and assist in establishing monitoring plans as assignedReview progress of projects and initiate appropriate actions to achieve target objectives.Perform and track project specific and therapeutic trainings for European CRAs/newly assigned team membersParticipate in the development of protocols, patient information documentation, Case Report Forms, project plans/reports and manuals as assigned.Interact with internal work groups to evaluate needs, resources and timelines.Act as primary contact for clinical trial supplies and other vendorsResponsible for all aspects of registry management as prescribed in the project plans.Review and approve reports for assigned repartees within countries/regionsPerform accompanied field visits/QC visits with assigned staff.