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Job Details

Global Clinical Trial Manager

Company: DOCS Global
Location: United Kingdom
Reference: Ref AS-016466
Closing Date: 25 Oct 16
Type: Contract
Salary (£): Competitive
Benefits: Excellent & Comprehensive

Job Summary:

DOCS has partnered with a highly prestigious organisation with one of the most robust pipelines in the industry. This is a fantastic opportunity for an experienced Global Project Manager who is ready to take on a new challenge, develop their career and enjoy a flexible working culture in our vibrant offices in either Marlow, Buckinghamshire or Eastleigh, Hampshire.


Roles & Responsibilities of the position

Key Responsibilities include:
• Leading and continually reviewing risk mitigation activities to ensure study delivery to plan
• Contributing to study-level risk assessments
• Identifying and resolving issues at a global level
• Reporting study progress at appropriate forums and to management
• Collaborating with Regional CTM 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
Critical Success Factors for the Role include:
• Working knowledge of International Conference on Harmonization (ICH), Good Clinical Practice (GCP), and applicable international regulations and guidelines
• Strong knowledge of Clinical Development process and procedures
• 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

Job Requirements

Requirements and Qualifications:
• BA/BS/BSc or RN
• Broad experience working in life sciences or medically related field
• General biopharmaceutical clinical research experience obtained working on clinical trials in a biotech, pharmaceutical or CRO company
• Experience in oversight of outside clinical research vendors (CROs, central labs, imaging vendors, etc.) highly preferred
• Eligibility to work and live in the UK

Key Competencies:
Project Management / Risk Assessment / Critical Thinking and Planning / Matrix Team / Organizational Leadership / Metrics Analysis / Strong Written and Oral Communication / Delivery Focus / Decision Making / Relationship Management / Conflict Resolution / Problem Solving / Adaptability and Flexibility

Remuneration & other details

What is offered:
• Permanent contract of employment
• Full-time
• Office-based and/or home-based
• Market leading salary based on level of skills and experience, plus company benefits (25 days annual leave, pension, life assurance, healthcare cover + discretionary bonus)

Training and development:
Full on boarding and training will be provided.

Apply for this job: Global Clinical Trial Manager

Contact Information:

Address:  DOCS UK
2 Globeside, Globeside Business park Marlow
Reasons to work for Docs International
Tel:  +44 (0) 2380 688500
Fax:  +44 (0) 2380 688501
Website:  Visit Our Web Site

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