Clinical Trial Manager (Global Studies) - Office-based Bucks/ UK

Recruiter
Docs International UK Limited
Location
Southampton
Posted
10 Feb 2018
Closes
15 Feb 2018
Sector
Healthcare
Contract Type
Permanent
Hours
Full Time
Clinical Trial Manager (Global Studies)- Office-based 3 days per week either in Buckinghamshire or Hampshire,

with 2 days home working

- Do you have experience of managing international studies within a CRO or pharma setting?

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

- Do you have full service/study oversight experience?

Our client is looking for a dedicated and motivated clinical trial manager to join their well-established team of international trial managers.

The 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 guidelinesWhat 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 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 Marlow (Bucks) or Eastleigh (Hampshire) office3 days per week with the flexibility of 2 dayshome-working;
- 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 ********************************* or ring +33 964 25 67 65.

*Applicants who have not had a response within two weeks

should assume their application has been unsuccessful*

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