Clinical Trial Manager / Global Studies / Hampshire / UK

Docs International UK Limited ,
Eastleigh, Hampshire
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Overview

Our client is looking for a dedicated and motivated clinical trial manager with study management experience across several countries. The successful candidate will join a highly dynamic team. Do you have experience managing international studies within a CRO or pharma setting? Do you have strong study planning and management experience to meet study deliverables and budget? Do you have full service/study oversight experience? If you do, please apply. The Clinical Project Manager/Clinical Trial Manager main responsibilities will include: · Planning and management of clinical studies conducted by global development team through the leadership of the cross-functional clinical study team · Contributing to study-level risk assessments · Leading and continually review risk mitigation activities to ensure study delivery to plan · Identifying and resolving issues at a global level · Reporting study progress at appropriate forums and to management · Collaborating with Regional Clinical Trial Manager to ensure country level study delivery aligned with global delivery plans · Overseeing global insourcing/outsourcing partner deliverables to the required standards · Managing study-level budget and timelines · Partnering with Tech Services, Supplier Governance and Electronic Trial Operations - to ensure vendor set-up, conduct and quality oversight of deliverables · Leading global study-level documentation and required tool and systems set-up · Leading development and implementation of global Drug Supply Plan · Ensuring implementation of study(ies) in accordance with SOPs and ICH/GCP guidelines What is required · BA/BS/BSc or RN · Previous experience of project managing international/global commercial clinical studies within the clinical research industry, i.e. within pharma, CRO or biotech working environments · Previous clinical study management/clinical project management as a Clinical Study Manager · Experience in overseeing external clinical research vendors (CROs, central labs, imaging vendors, etc.) highly preferred · Project management experience including oversight of study deliverables, budgets, and timelines · Ability to use scientific and clinical knowledge to conceptualize study designs · Experience anticipating and resolving problems · Experience writing and presenting clearly on scientific and clinical issues · Experience collaborating and leading cross-functional teams (team/matrix environment) · Knowledge of project risk management assessment and mitigation approaches Full-time availability Full and valid UK working eligibility Full and valid driving licence Ideally able to start ASAP/negotiable Key competencies · Project Management · Risk assessment · Critical Thinking and Planning · Matrix Team organization/leadership · Metrics analysis · Written and oral communication · Delivery focus · Decision Making · Organizational savviness · Relationship management · Conflict resolution · Problem solving · Adaptability and flexibility What is offered Permanent contract of employment with DOCS seconded to the client; Full-time; The role is office-based at either the Eastleigh (Hampshire) office, 3 days per week with the flexibility of 2 days’ home-working; Competitive salary depending on level of skills and experience; Company benefits: 25 days’ annual leave, car allowance, bonus, p ension and healthcare. Why Join DOCS? If you are an experienced clinical study/trial manager with solid clinical research industry experience, contact me now for more details with your latest CV . Applicants who have not had a response within two weeks should assume their application has been unsuccessful This job was originally posted as www.totaljobs.com/job/89880578

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