DOCS Global

Clinical Trial Manager / Global Studies / Buckinghamshire / UK

Location
Marlow, United Kingdom
Salary
Competitive
Posted
03 Jul 2019
Closes
02 Aug 2019
Ref
Ref AS-029624
Discipline
Clinical Research
Hours
Full Time
Contract Type
Contract
Experience Level
Experienced (non-manager)


Job Summary

This an a great career opportunity for an experienced clinical study manager looking for their next step up. The role offers a fresh challenge and the opportunity to manage global international commercial clinical trials. For full details, 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*

Roles & Responsibilities of the position

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

Job Requirements

• 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

Remuneration & other details

• Permanent contract of employment with DOCS seconded to the client;
• Full-time;
• The role is office-based at either the Marlow (Bucks) office or 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, pension and healthcare.

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