Global Study Manager / Permanent / UK

Clinical Trial Manager (Global Studies)

• Do you have experience of managing international commercial clinical studies within a CRO or pharma setting?

• Can you demonstrate strong planning and management skills to meet study deliverables and budget?

• Do you have global study oversight experience?
• if you do, please apply now.

The Clinical Trial 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 guidelines

  What is required

• 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 Trial or 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

What is offered

• Permanent contract of employment with DOCS seconded to the client;
• Full-time;
• Office-based near Southampton (Hampshire) with the flexibility of up to 2 days’ home-working per week.
• 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/trial manager looking for a new career opportunity with a rapidly growing and fast paced global leader, please send your CV today to me or for more details: Elisabeth.Knighton@docsglobal.com or ring +33 964 25 67 65.

*Applicants who did receive a response within two weeks should assume their application has been unsuccessful*