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Freelance Clinical and Regulatory Start Up Manager - Oferta z Jobs.pl

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Freelance Clinical and Regulatory Start Up Manager

Nr ref.: /JOBS.pl

  • Role: Clinical and Regulatory Start Up Manager

    Location: Anywhere in Europe

    Contract: 6 months - 1 year

    Are you looking for a change? Looking to make a difference, check us out!

    Premier Research helps highly innovative biopharmaceutical and medical device companies transform life-changing ideas into reality. We take on the most challenging areas of study, with a special focus on unmet needs in such areas as analgesia, CNS, rare diseases, medical device and diagnostics, and pediatric research

    We're looking for a strong Freelance Clinical and Regulatory Start Up Manager to join our team! You will be required to ensure the continuous improvement of quality of all Regulatory and Start-up components at the project level. This is a global position and can be located anywhere in Europe.

    You will need to start immediately and have 0.5 - 1.0 FTE availability.

    You'll be accountable for:

    Preparing Core Clinical Trial Applications for competent authorities
    Driving the overview of applications done by Start-up Managers to competent authority (CA) and Ethics Committees /IRBs
    Producing or reviewing some submission components like the Patient Information Form/ICF and or Investigational Medicinal Product Dossier (IMPD) or equivalent document as required
    Maintaining good, friendly and professional relationships with past, current and potential sponsors
    Contributing to the business development process by reviewing proposals, budgets and attending client meetings
    Keeping abreast of scientific developments and maintain technical expertise
    Working with the PM to understand financial aspects of the project; cascades to all start-up team members the number of hours/tasks available per contract; monitoring project performance

    You'll need this to be considered:

    Education to university degree level in pharmacy, medicine or related natural sciences
    Strong experience, including previous experience in Regulatory or Start-up functions ideally on a global level
    Hands-on experience in the submission of clinical trial applications
    Ability to multitask and work effectively in a fast-paced environment with changing priorities
    Maintains a positive, results orientated work environment
    Ability to read, write, and speak fluent English

    If you are looking for a career within a transparent and non-hierarchical organisation then please contact us at the email address listed below. We are open minded and flexible regarding the talent we recruit, ultimately we are looking for people who will share in our vision and realise the importance of communication, building relationships and adhering to the highest quality standards.

    Please note:- You must be eligible to live and work in the specified European country in order to apply for this role.

    Keywords:- Clinical and Regulatory Start Up Manager, Regulatory Start Up Specialist, RSU, Start Up, Regulatory, Permanent, Global, Office Based, Europe, Home Based, Contract Research Organization, CRO, Clinical Research, Clinical Trials, Pharma, Bulgaria, Poland, Spain, Italy, Germany, UK, France, Belgium, Netherlands, Ukraine, Czech Republic, Austria

    More: #.V-poG_krLIU#ixzz4LSXaG8I5


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