Pharmiweb ChannelsAll | PharmaCo | Clinical Research | R&D/BioTech | Sales/Mktg | Healthcare | Recruitment | Pharmacy | Medical Comms

Pharmiweb.com RSS Feed Pharmiweb.com RSS Feeds

Job Details

Clinical Trial Manager, global studies (Office-based Bucks) UK

Company: DOCS Global
Location: Marlow or Eastleigh
Reference: EK-gctm
Closing Date: 07 Jun 18
Type: Permanent
Salary (£): On Application
Benefits: car allowance, bonus, etc

Job Summary:

•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?

Requirements:

Clinical Trial Manager (Global Studies) - permanent

Office-based 3 days per week with with 2 days home working at either the Buckinghamshire or the Hampshire office.

  • 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 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 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

What is offered

Permanent contract of employment with DOCS seconded to the client;

Full-time;

The role is office-based at either the Marlow office in Buckinghamshire or at 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.

 

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 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*

 

Apply for this job: Clinical Trial Manager, global studies (Office-based Bucks) UK

Contact Information:

Address:  DOCS UK
2 Globeside, Globeside Business park Marlow
SL7 1HZ
England
Reasons to work for Docs International
Tel:  +44 (0) 2380 688500
Fax:  +44 (0) 2380 688501
Website:  Visit Our Web Site

Advertising
Site Map | Privacy & Security | Cookies | Terms and Conditions

PharmiWeb.com is Europe's leading industry-sponsored portal for the Pharmaceutical sector, providing the latest jobs, news, features and events listings.
The information provided on PharmiWeb.com is designed to support, not replace, the relationship that exists between a patient/site visitor and his/her physician.