DOCS Global

Local Trial Manager *** UK***

Location
Istanbul, UK
Salary
Competitive
Posted
19 Mar 2021
Closes
14 Apr 2021
Ref
27745
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
Are you looking for a new role as Local Trial Manager within a large international pharmaceutical company? DOCS Global is hiring an experienced Local Trial Manager.
This role is permanent.
Description
• Responsible for country do-ability (if applicable) and site feasibility assessment in conjunction with CTA (if applicable), SM and GTM. Implements any local criteria for site selection. Ensure consistent conduct of pre-trial assessment visits and instruct teams on appropriate follow-up of pre-trial visit report and country feasibility report. Recommends suitable sites for selection to participate in trial.
• Collaborate with the CPL, GTM, local management/Country Head and Protocol Owner to select final site list.
• Lead and coordinates local trial team activities in compliance with GCO Standard Operating Procedures (SOP), Work Instructions (WI) and applicable regulations.
• Lead local project planning activities to meet recruitment targets and to deliver high quality data on time and within study budget. Including but not limited to: development of local trial specific procedures and tools, recruitment planning, contingency and risk management, and budget forecasting.
• Ensure that all SAEs/PQCs are reported within reporting timelines and documented as appropriate.
• Monitor country progress and initiates corrective and preventive actions when the trial deviates from plans and communicates study progress and issues to study management teams.
• May submit requests for vendor services and may support vendor selection
• May lead negotiation of trial site contracts and budgets, with the assistant from a LTM II or III. Forecasts and manages country/local trial budget to ensure accurate finance reporting and trial

Your Profile:
• A degree in a health or science related field is preferred.
• Must have experience in Clinical Research or equivalent qualification
• At least 1,5 years' experience in a similar position
• Strong working knowledge of ICH-GCP, company standard operating procedures, local laws and regulations, assigned protocols and associated protocol specific procedures including monitoring guidelines.
• Strong IT skills in appropriate software and company systems. Willingness to travel with occasional overnight stay away from home.
• Good written and oral communication skills.

If you think this is the job for you, please send your application to Stephanie: Stephanie.broize-arrieu@docsglobal.com

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