Clinical Project Manager, One Health
vor 6 Tg.

What if you could work for a cause, not just a company?

At Novozymes OneHealth, we are on a quest to help people live healthier and better lives, by rethinking tomorrow within human health, and finding the one-in-a-trillion verifiable solutions of probiotics and enzymes that can be proven to solve profound health challenges related to modern lifestyles.

We have started rethinking tomorrow within human health; thinking outside the box, working in new ways, building different partnerships, pioneering data science and digital approaches, discovering ground-breaking science and much more do you want to join our great team?

OneHealth is a newly established Strategic Opportunity Area within Novozymes working as a corporate venture with a start-up mindset.

We are a high-energy team with diverse backgrounds on a mission to develop solutions within gut and oral health aimed at the consumer care space.

We focus on probiotic- and enzyme-based solutions and drive development based on strong scientific hypotheses and identified consumer demand.

Join us as our new Clinical Project Manager, OneHealth

Have you ever wanted to make a difference to the health challenges we all face in this fast-living and constantly changing world?

This is your chance! We are building a business in human health linking Novozymes unique technology position and culture to products and routines that impact most people’s lives.

We are seeking a strong Clinical Project Manager to manage human clinical trials aimed at demonstrating the health benefits of our products.

In this role, you will work with a diverse team of scientists and business experts to design clinical trials aligned with scientific opportunities, commercial needs, and regulatory frameworks.

As a key member of the team you will advise project teams throughout the project life cycle from a clinical development point of view.

Once a project is ready to enter the clinical development phase, you will be in charge of the whole process including the writing of trial protocols, selection and management of CROs and keeping all stakeholders updated on clinical trials progress.

This position is exciting as it engages you at all parts of the project and allows you to see it from start to finish, all the while working with highly professional, driven, and fun colleagues.

In this role you’ll make an impact by :

  • Organizing, planning, and effectively executing clinical trials with health food ingredients aimed at supporting health claims and product launches.
  • Guiding scientific project teams and business developers from early discovery through to initiation of clinical trials to ensure that all work done aligns with the ultimate clinical trial objectives and complies with GCP standards and other regulatory requirements.

  • Leading the writing of relevant clinical trial documents like synopsis, protocols and investigator brochures
  • Identifying, evaluating, and selecting suitable contract research organizations and / or investigators for the execution of clinical studies.
  • Managing the relationship with CROs or investigators and oversee budget and timelines during the clinical trial.
  • Coordinating the preparation and review of all operational trial related documents.
  • Supporting QA with the conduct of onsite audits at CROs and trial sites.
  • Managing all planning and communication regarding clinical trials with commercial partners in case of co-development clinical studies.
  • Effectively communicating and presenting results to relevant stakeholders.
  • Contributing to the evaluation and publication of clinical trial data.
  • Contributing to the great OneHealth culture we have built and are proud of!
  • To succeed you must have :

  • A master’s degree or higher in life sciences or a related scientific domain.
  • At least 3 years of experience at managing human clinical trials in a pharma or a food company or at a CRO.
  • Full understanding of GCP principles.
  • Strong project management, organizational and communication skills.
  • Demonstrated ability to build collaborative relationships with key internal and external partners and stakeholders
  • Technical writing skills
  • Proven track record of effective project execution with a passion for delivering impact for patients and consumers.
  • Capability to work on several complex projects at the same time with flexibility and organization.
  • An entrepreneurial spirit and drive, ability to thrive in uncertainty and constant change and willingness to do what is required to make things move forward
  • A can-do-attitude and a great work ethic balanced with good humor and a zest for life.
  • Excellent oral and written English skills. Knowledge of any other major language is a plus.
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