DOCS Global

Global Study Manager / Permanent / UK

4 days left

Hampshire (GB)
competitive salary - great team - solid and stable company
09 Feb 2021
11 Mar 2021
Full Time
Contract Type
Experience Level

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: or ring +33 964 25 67 65.

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

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