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CSL Confidential Active Jobs Report dated: Wednesday, May 22, 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'.

R&D Clinical Outsourcing Manager

CSL Code: 7577

Job Title
R&D Clinical Outsourcing Manager
Target Compensation
Day Rate/Negotiable, Confidential
Job Type
Clinical Contracts & Outsourcing, Clinical Study Monitoring/Leadership, Clinical Study Management/Operations, Clinical Project/Program Management, CRA Management, Finance/Bids/Proposals, Project Control & Budgets
Location
Bedfordshire, Berkshire/Buckinghamshire, Middlesex, Surrey, South London, West London, Humberside, Tyne & Wear, Yorkshire, Cheshire, Cumbria/Lancashire, Greater Manchester, 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
Tue 31st July 2012, 05:13pm
Position R&D Clinical Outsourcing Manager - Permanent
FMCG Company in the North East or Berkshire

Introduction

Our client's health, home and hygiene brands are sold in over 180 countries around the world.
Their entrepreneurial and creative people drive its marketing, sales, research and development programs
Our clients and strategy and vision are a world where people are healthier and live better.
Our client's purpose is to make a difference by giving people innovative solutions for healthier lives and happier home.

If you feel you share their ideals please read on

Job Summary

In this instrumental role you will search for new CROs and clinical suppliers globally that will both match our clients business and clinical trial programme needs as well as enabling development of and trial of new clinical trial methodologies. An equally important part of this role will be to review costings of all clinical programes globally and become involved in reducing costs whilst also maintaining quality and timelines. You will also lead discussions on cost, efficiency and synergies, driving down the overall cost of our client's clinical trial programmes.

Key Challenges

To continually monitor CROs and Clinical suppliers to ensure that our client is aware of new services and new capabilities and to ensure that our client have a global breadth of high quality CROs and clinical suppliers that cover all our trial phases and types.
To work with the clinical team on^anticipating which trials are on the horizon and ensure our client has a suitable CRO or clinical supplier that has both the methodologies and location to best meet their requirements.
Working with the other relevant internal experts to effectively^assess the capabilities and standards of potential new CROs globally and influence internally for trials to be placed with them
To be aware of and feedback to the business on relevant clinical trial centres of excellence / expertise for relevant therapeutic areas / methodologies.
Impact and influence on senior managers within the business.

Essential Skills & Qualification

Appropriate scientific &/or medical degree with broad clinical and consumer healthcare (or pharmaceutical) industry^knowledge and experience
Significant depth and breadth of clinical trial expertise and operational experience including trial design, protocol development, trial monitoring and clinical project / CRO management
Proven ability to drive down clinical costs through negotiations with customers &/or CROs
CRO assessment and audit experience, preferably at a global level (or experience within a global CRO)
Knowledge of international regulatory frameworks as they relate to clinical requirements for product registration
Strong understanding of planning, budgeting, priority setting, project management

Supplementary Requirements:

Software Competence: MS Office, MS Project,
Valid Driving License: Essential
Working Language(s): English
Flexible Working Hours: No

Employment Information:

Employer: Pharmaceutical Company
Employment Type: Permanent
Hours: Full time
Location: Berkshire or East Yorkshire
Plan Start Date: Negotiable
Employer Benefits:
Company Pension, Life^Insurance, Private Healthcare, Dental Care, Flexible Package Plan, Stock Options/Purchase Plan, Bonus, Free gym, Free Bus, Childcare Vouchers. Relocation Assistance.

Keywords:

MS Office, MS Project,Clinical Research, Clinical Operations, Clinical R&D, , CTM, CTA, GCP, , CRO Manager, Study Manager, EUCTD, ICH GCP, Project Manager, Clinical Study, Feasibility , Essential Documents, GCP, SOPs

Assigned Consultant: Stewart Hulse at CSL Recruitment on 01932 228928
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 demonstrate the skills the role requires in their application. The role may be remarketed; if you applied for this role previously and were unsuccessful you will not receive a response. We request that non EU Nationals include evidence of right to work in the country concerned with their application to be considered. Do supply supplementary information on required location, notice period and expected salary/day rate if you are a new candidate

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