Hobson Prior are currently working with a multinational pharmaceutical and life sciences company whose products and services are designed to benefit people and improve their quality of life. Our client is looking for a Country Lead Monitor/LTM to join them on a permanent basis in London.

Job Responsibilities:

• You will act as the key country study contact for the core study team and overall responsible for country deliverables regarding timelines, budget and quality for assigned studies from feasibility all the way through archiving.
• Establishes proper collaboration with local functions such as medical affairs, pharmacovigilance, regulatory, legal, compliance to ensure the study is conducted in accordance to local requirements and regulation.
• Responsible to align the relevant stakeholders internally and externally, to support regulatory and country start-up activities and to coordinate quality initiatives.
• May be assigned to be the primary liaison for CRO and ARO-run studies.
• Accountable for the overall quality of the study in his/her country by using relevant IT systems, among other tools.
• May act as a mentor for new or less experienced CRAs and CLMs.
• May be assigned to specific local and global expert working groups, roles, initiatives or other activities at the discretion of the CHSM.
• Accountable for planning, managing and tracking local study budget in close liaison with the assigned CTPS specialist as well as the core study team.
• Identifies budget/estimate issues and proactively develops a plan until resolution.
• Any other assigned duties.

Key Skills:

• Effective written and verbal English communication skills, strong oral presentation, interpersonal, decision-making and issue resolution skills are required.
• Excellent planning and organization skills, attention to detail and excellent follow through.

Requirements:

• Must have a bachelor's degree (or equivalent) with 6 - 7 years of relevant healthcare experience including 4 years of monitoring & site management experience.
• In-depth knowledge of the drug development process including monitoring and site management, local and international regulations, ICH - GCP, drug safety requirements, data management processes and investigator grant parameters.
• You will have awareness and an understanding of cultural differences as well as regional operational differences and budget management.

Apply now:

If you are interested in learning more or applying to this exciting opportunity then please click "Apply" and upload a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist directly, please select "Contact me" at the top of this page.

Hobson Prior is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Hobson Prior is acting as an Employment Agency in relation to this vacancy.