logo

+44 208 985 0565

Senior Vice President Clinical Operations


This job does not exist anymore.

Try running a new search or browse our vacancies.

Or fill in the form below to receive job alerts.

https://www.pop-science.co.uk/1181-senior-vice-president-clinical-operations/clinical-research/central-london/job2020-11-04 17:57:521970-01-01 Pop Science
Job Type Permanent Full Time
Location London
Area Central London, UK Central London UK London
Sector Clinical Research
Salary Based on experience
Currency gbp
Start Date ASAP
Advertiser remoteapi
Job Ref 962
Job Views 661
Description

We are delighted to be partnering with our client, a fast growing and profitable medical data analytics company, providing data management and advanced analytics to the pharmaceutical clinical trials market, to help them find an expert Clinical Operations Leader to head up their team as the Senior Vice President Clinical Operations.

It's a great opportunity to join a market leading company at the Senior Leadership level. You will get to lead and develop your own team, which is the largest in the company. You therefore need to know what excellence looks like and be able to model this. You would also need a strong background in delivering to clients, including working with business development and other functional teams to develop and deliver outstanding services.

Purpose of the Role

  • Operational leadership bring a delivery orientated culture to the Clinical Operations team;includes clear planning, scheduling and "on budget" delivery of both client projects and internal operational improvements
  • Expected to bring "best in class" industry expertise and a track record of being able to diagnose operational areas of most impactful operational improvements to service level and company P&L. The candidate is expected to significantly enhance capabilities to scale and deliver on ambitious growth plans.
  • Participate at the Senior Leadership level to deliver Clin Ops services
  • Work with Business Development ito win new clients, by pitching operational capabilities to support all phases of clinical trial, globally. Includes identifying opportunities to expand operational footprint in support of growth; in particular in North America.
  • Contribute to the annual growth strategy reviews including, supporting the CEO in operational due diligence in of potential M&A opportunities

Budget Responsibilities:

  • Forecasting and delivery of total revenues, cost of sales and gross profit/margin.
  • Forecasting resources, costs and timelines for new client projects 
  • Forecasting and delivery of grant income and expenditure.
  • Individual project financial performance (project revenues/income, costs and gross profit/margins) & client governance KPI's.
  • Staff budgets. Clinical Operations cost centre, including all internal resources, third-party supplier, conference/travel and training costs.
  • Motivate and develop talented individuals within the department; whilst addressing development or performance issues identified early in order to optimise organisational performance. 

Personal attributes, experience & qualifications:

  • An individual who can think strategically, sees more than one route to a solution.
  • An individual able (and willing) to roll up their sleeves and work with the team to address bottlenecks, system inadequacies and unnecessary complexity. I.e. Able to be strategic and also take a 'Hands On' approach to make things happen when required.
  • Has the gravitas to engender confidence at Board level and externally to clients or partners
  • A strong people manager, someone who looks to build a high performing team by hiring staff who are at least as good as they are if not better.
  • Comfortable in the detail but not obsessed by it.
  • Strong experience in a Clinical Operations leadership role with responsibility for a wide range of technical functions.
  • A track record of developing and implementing successful operational strategies within the clinical trials, outsourcing market. Requires evidence of a proven track record of managing the delivery of technical services in multiple geographies across all phases of clinical trials to the global pharmaceutical industry
  • Experience and familiarity in operating within a metrics governance framework and formal continuous improvement programmes.
  • Experience of formulating & executing continuous improvement initiatives in a highly regulated business environment to deliver enhanced service levels more efficiently, first time.
  • Formal training or experience of Lean (e.g. Six Sigma) programs would be highly beneficial in the role.
  • Experience in working across international boundaries and time zones in support of the global pharmaceutical industry; understanding of the North American and European CRO landscape (knowledge of the Asian market would be a plus)
  • Excellent line management skills and able to set clear direction of expectations at a departmental and individual staff level.
  • Ability to demonstrate a track record of achieving extraordinary results
Keywords
SectorClear
AreaClear
Job TypeClear
SalaryClear
CurrencyClear
Sign in
Register
Similar Jobs
  • CMC Regulatory Affairs Consultant
    UK, Central London
    Clinical Research
    £0 per year

    Position Summary

    We are seeking an experienced freelance CMC Regulatory Affairs Consultant to support the development, submission, and lifecycle management of regulatory CMC documentation for biologics, pharmaceuticals and/or advanced therapies. The consultant will provide strategic and ope...

  • Non-Clinical Expert/Signatory
    UK, Central London
    Clinical Research
    £0 per year

    Freelance Non-Clinical Expert (EU/UK-Based)

     

    We are seeking an experienced freelance Non-Clinical Expert to act as a regulatory signatory for non-clinical overviews in the EU/UK. The ideal candidate will be capable of reviewing and signing non-clinical reports and non-clinical s...

  • Senior Medical Device Consultant (with SaMD)
    UK, Central London
    Clinical Research
    £0 per year

    We are seeking a freelance Senior Medical Device Consultant with experience in class I-III medical devices and software as a medical device (SaMD). The successful candidate should have a thorough knowledge and understanding of the Software Life Cycle processes, be able to conduct thorough technic...

Email Me Jobs Like This
Subscribed to similar jobs notifications
We use cookies to provide you with the best possible browsing experience on our website. You can find out more below.
Cookies are small text files that can be used by websites to make a user's experience more efficient. The law states that we can store cookies on your device if they are strictly necessary for the operation of this site. For all other types of cookies we need your permission. This site uses different types of cookies. Some cookies are placed by third party services that appear on our pages.
+Necessary
Necessary cookies help make a website usable by enabling basic functions like page navigation and access to secure areas of the website. The website cannot function properly without these cookies.
ResolutionUsed to ensure the correct version of the site is displayed to your device.
essential
SessionUsed to track your user session on our website.
essential
+Statistics
Statistic cookies help website owners to understand how visitors interact with websites by collecting and reporting information anonymously.
Google AnalyticsGoogle Analytics is an analytics tool to measure website, app, digital and offline data to gain user insights.
Yes
No
Money Penny
Yes
No

More Details