DOCS Global

Global Clinical Project Managers

Location
Southampton Hampshire, Southampton Hampshire
Salary
Competitive
Posted
28 May 2021
Closes
27 Jun 2021
Ref
29515
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
You will demonstrate study management experience across several countries and multiple regions.

You will join a highly dynamic team of global clinical trial managers and join one of the most dynamic global study management team.

The Clinical Project 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

What is required

• BA/BS/BSc or RN
• Previous experience of project managing international commercial clinical studies within the clinical research industry, i.e. within pharma, CRO or biotech working environments, ideally 5 to 7 years.
• 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 and valid UK working eligibility
• Ideally able to start ASAP/negotiable

What is offered
• Permanent contract of employment with DOCS seconded to the client;
• Full-time;
• The role is office-based either near Southampton (Hampshire, UK) 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.

For more details please contact me at Elisabeth.Knighton@docsglobal.com or ring +33 964 25 67 65.

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