Alexandra Sharp Email & Phone Number

United Kingdom

United Kingdom

• High-priority trial Ex-US Medical Science Liaison Lead (WW).A member of WW Core Field Medical team at international congresses.Organiser and a participant in scientific advisory boards, roundtables and preceptorship.
• Engagement with Healthcare Professionals:Develop and maintain relationships with Thought Leaders and Healthcare Professionals to answer scientific questions;Effectively present information to HCPs (1:1, group.
• Contribute to the Medical Plan:Create and implement territory Field Medical plans and thought leader interaction strategies aligned with therapy area objectives.
• Provide Medical Support:Deliver training and key scientific updates to internal stakeholders and provide scientific support at external meetings.
• Clinical Trial Support: Identify and assess potential study sites, facilitate patient recruitment and support investigators throughout the process.

United Kingdom

• Clinical sites’ main point of contact, accountable for quality and delivery of sites from Initiation to Close out of the trial. Oversee the conduct of the trial at designated sites ensuring the rights and well-being of.
• Build relationships with investigators and site staff.
• Facilitate and support site with access to relevant study systems and ensure sites are compliant with project specific training requirements.
• Address and resolve issues at sites. Determine and implement appropriate follow-up action.
• Perform and report on-site visits and remote contacts in accordance with the monitoring plan.
• Assess & manage test article/study supply including supply, accountability and destruction/return status.

United Kingdom

• Experience in Phase 3b - 4 clinical study development and start-up process (regulatory submissions at country & site level according to local requirements; support with contract negotiation) including initiation and.
• Responsibility for initiating and conducting initial and ongoing site, sponsor, and project staff clinical trials related training.
• Initiating new clinical sites and ongoing monitoring of clinical study progress (onsite and remotely) to ensure compliance with study protocol requirements, appropriate research ethics committee, government health.
• Experience in monitoring and tracking patient enrolment to ensure timely and accurate study data collection, including addressing data clean-up and data query resolution.
• Responsibility for tracking and maintaining clinical trial associated documents and payments, and also project related supplies.
• Assist the Study Sponsor/Project Team with problem solving and provide direct consultation on study related activities.

Reading, United Kingdom

Worked in the Real World Late Phase Research department as the primary point of contact with sites in phase 3b, 4 and observational research. Performed site selection, start-up, initiation and remote monitoring to ensure the proper conduct of the study protocol. Responsibilities included start/up regulatory submissions to the Competent Authority and Ethics.

Cosham, Portsmouth, United Kingdom

Clinical placement in Obstetrics & Gynaecology.

Saint Petersburg, Russian Federation

Clinical internship in gastroenterology, cardiology, pulmonology, allergology, endocrinology and cardiac electrophysiology.

Saint Petersburg, Russian Federation

While studying I worked part-time as a Front Office Manager for a private hospital. My role included liaising with patients, doctors and international insurance companies. I organised and translated documents as well as arranged appointments and treatments.

Saint Petersburg, Russian Federation

Bachelor Of Medicine (Mbbs), Medicine

Physician, Internal Medicine

Clinical internship in Internal Medicine.