Associate Project Setup Manager

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Company Description

Eurofins Scientific is an international listed life sciences company that provides its customers with high-quality laboratory research and advice. Eurofins is a real start in bio-analytical testing for food, water, environment, cosmetics, pharmaceuticals and contract research for agroscience. In addition, Eurofins is one of the world's largest providers of testing and laboratory services in genomics, forensics, CDMO, advanced materials science, drug development and clinical studies. Eurofins uses a unique amount of analysis methods and an unprecedented high level of knowledge and expertise.

Eurofins consists of more than 50,000 employees worldwide, spread over 800 state-of-the-art laboratories and is active in 50 countries with a pro forma turnover of €5.4B in 2020. Eurofins has strong growth ambitions (CAGR 24%). In addition to very strong organic growth with many of its own start-ups, Eurofins also made a large number of acquisitions in various countries last year.

Our people at Euros make an important contribution to issues such as the environment, food and general health. Employees are proud of the work they do and experience a lot of freedom in the performance of the job. Responsibilities are as low as possible in the organization so that the people with the right information can start taking the right ones. Eurofins invests structurally in the personal development of talent, both in the field of leadership, growth potential and substantive knowledge.

Eurofins Central Laboratory is a dynamic, strong organization that offers laboratory services worldwide. supporting us the pharmaceutical and biotechnology industry with a full suite of central laboratory services. In addition, we provide extensive support in Biomarkers, Bioanalysis of Small and Large Molecules, Immunogenicity, Microbiology and Genomics. Our facilities are located in the US, Europe, Singapore, China and India.

Job Description

Perform accurate and timely study configurations in database system to enable delivery of central laboratory services to Sponsor and investigators according to protocol requirements. Produce individual project specifications and configure investigator deliverables that are correct and have sponsor approval.

Key Accountabilities

  • Timely configure the central laboratory project into an operational database by translating the clinical protocol objectives into technical requirements.
  • Produce correct specifications reflecting the signed clinical protocol, signed contract and budget. In line with the specifications, define the investigator deliverables: Investigator Laboratory Manual (electronic or paper), kit and requisition form.
  • Contribute to discussions on study setup specific topics both internal and with the Sponsor to get the best solution for the study.
  • Perform timely, accurate changes to project configuration and investigator deliverables that meet signed amendments and internal guidelines, maintaining consistent documentation throughout.
Qualifications
  • Minimum of 1 years’ Project Management experience in complex project service industries.
  • Minimum of 1 years’ relevant clinical project experience with a CRO or Sponsor organization.
  • A Bachelor degree in Healthcare / Life sciences along with significant industry experience.
  • Analytical: is able to visualize, articulate, conceptualize or solve both complex and uncomplicated problems by making decisions that are sensible given the available information. Such skills include demonstration of the ability to apply logical thinking to breaking complex problems into their component parts.
  • Customer and Result Orientation: takes personal responsibility for decisions and delivering results, takes actions and decisions in case of customer needs, sets and achieves achievable goals; complies with quality, service and productivity standards and meets deadlines.
  • Good communication and interpersonal skills.
  • Energetic and enthusiastic with a flexible and dynamic work ethic.
  • Good at establishing and maintaining internal and external relationships.
  • Excellent command of English, spoken and written.
Additional Information

Are you the driven, proactive colleague we are looking for and would you like to join our team? We would like to receive your CV including motivation via the application button.

Dienstverband:
fulltime
Type vacature:
Intern

Vaardigheden

  • Er is geen minimale opleiding vereist

Wat wij bieden

Contract:
Fulltime
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