Roles & Responsibilities of the positionThe Clinical Project Manager key 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 guidelinesJob Requirements• BA/BS/BSc or RN • Previous experience of project managing international/global commercial studies within the clinical research industry, i.e. within pharma, CRO or biotech working environments • Previous 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 flexibilityRemuneration & other details• Permanent contract of employment with DOCS seconded to the client; • Full-time; • Home-based or office-based at either Marlow (Bucks) or Eastleigh (Hampshire); • Competitive salary depending on level of skills and experience; • Company benefits: 25 days annual leave, car allowance, bonus, pension and healthcare. Why Join DOCS? If you are an experienced clinical study/clinical trial manager professional looking for a new career opportunity, please send your CV today to Elisabeth.Knighton@docsglobal.com or ring +33 964 25 67 65. *Applicants who have not had a response within two weeks should assume their application has been unsuccessful.