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CSL Confidential Active Jobs Report dated: Tuesday, May 21, 2013

Review more information or apply at http://www.cslrecruitment.com/. Search for the CSL 4 digit code in orange using our Quick Job Search. To discuss a role, call our Candidate Hotline: 01932 219 320. Job status changes by the minute on the site and we recommend you apply via the site to ensure status is still 'Open for Applications'.

Senior Clinical Scientist, pharma, permanent

CSL Code: 7417

Job Title
Senior Clinical Scientist, pharma, permanent
Target Compensation
Day Rate/Negotiable, Confidential
Job Type
Clinical Study Management/Operations, Clinical Project/Program Management, Clinical Sciences/Genetics/Genomics, CRA Management, Project Control & Budgets
Location
Berkshire/Buckinghamshire, Middlesex, Oxfordshire, Surrey, Central/City, East London, North London, South London, West London, Hampshire/iow
Employment Type
Permanent Job
Employer Type
Biotech, Pharmacuetical Affiliate/Marketing Company, Pharmaceutical R&D HQ (Global Or EU)
Seniority
Senior Executive/Team Leader, Team Manager/Project Manager
Duration
 
FTE Hours
Full Time 35 - 40hrs Per Wk
Vacancy Status
Open For Applications
Date Posted
Wed 13th June 2012, 01:20pm
Senior Clinical Scientist- Permanent role
Phase II- IV European programme management
Major pharma based in Hampshire

Role

Superb positions with our client based in Hants, working on varied programmes of studies in several indications. This^is an excellent next step for individuals with study management experience in the EU and in complex indications, particularly those involving patient assessed efficacy criteria.

Our client is prepared to employ at different levels of experience for these roles so please call to review how your experience matches what they are seeking. To be considered at the more senior level, you must be able to demonstrate that you have written study protocols

Our client values:

Independent thinking
Problem solving skills
A cando attitude
Essential Skills & Qualifications Required
Previous experience of managing multi-centre clinical studies in the EU
Study management experience in Asia-Pac countries would be an advantage

All applicants^must have previous experienceof managing outsourced studies to vendors

B Sc as a minimum and ideally a higher degree
Demonstrated experience in a pharma headquarters, affiliate, bio-tech or international CRO managing studies in phases II - IV

Software Competence Required
Intermediate MSWORD
Intermediate EXCEL
Intermediate Powerpoint
Employer: Pharmaceutical Company
Employment Type: Permanent, full-time
Location: office based only in Hampshire

Keywords:

Clinical Research, Clinical Operations, Clinical R&D, CRA, CTM, CTA, GCP, Site Manager, Monitor, Manager, Study Manager, EUCTD, ICH GCP, Project Manager, Clinical Study, Clinical Programme, Feasibility Budget, vendor, RFP, variation, scope, outsource, CRO selection, Contracts, Clinical Trial Agreements, project manager, programme manager, clinical study protocol
Assigned Consultant: Gabrielle Gainsborough or Avril Horn at CSL on 01932 228 928
Please feel free to call for a detailed Job Description or additional information

Applications are reviewed within 24hrs, applicants will only receive feedback if they are suited to the role. The role may have been remarketed; if you applied for this role previously and were unsuccessful you will not receive a response. We are unable to respond to applicants who are notEU nationals unless they include evidence of right to work in full time employment with their application. Do apply with relevant information on required location or salary/day rate if you are a new^candidate.

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