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Project Coordinator, eCOA (f/m/d)

78% Flex
EXTRA HOLIDAYS - EXTRA PARENTAL LEAVE
Remote: 
Full Remote
Contract: 
Work from: 

Offer summary

Qualifications:

BS, BA or equivalent, Experience with customer service orientation, Healthcare or medical experience preferred.

Key responsabilities:

  • Provide customer support for Clario products in clinical trials
  • Collaborate with diverse project teams
  • Manage project issues and tracking metrics
  • Fulfill study-specific tasks in project phases
  • Ensure compliance and manage project aspects
Clario logo
Clario Biotech: Biology + Technology XLarge https://clario.com/
5001 - 10000 Employees
See more Clario offers

Job description

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Your missions

Join our PMO office as a Project Coordinator (f/m/d) and partner with Clario's Project Managers to coordinate eCOA clinical studies, ensure client satisfaction - and make a positive impact on patients' lives!

What we offer:

  • Competitive compensation

  • Attractive benefits (security, flexibility, support and well-being)

  • Engaging employee programs

  • Remote working & home office allowance

  • OTP Szép Card

What you'll be doing:

  • Deliver superior customer service by providing best business practices and support in using Clario’s products for the duration of client’s clinical trials

  • Work and collaborate with project team/s of diverse talents (Project Manager, Data Management, Archive team, etc) in development and delivery of Clario products to help clinical research industry obtain high quality data.

  • Pro-actively manage lifecycle of issues from being reported by customer to its resolution by the support and development teams.

  • Record and track key project monitoring and tracking metrics.

  • Meet regularly with clients via phone and/or web to provide weekly monitoring updates, track on-going issues and communicate project status.

  • Meet regularly with Team Leader to discuss workload, communicate project issues and address individual development.

  • Fulfill Project Coordinator study specific tasks during each phase of the project.

    • Development – (Study Documentation, Deployment Planning, Internal Training)

    • Monitoring – (Project Reporting, Issue management and resolution, Project process improvements, Mid Study Changes, Inventory management)

    • Close Out – (Data reconciliation and resolution, Inventory reconciliation, Study documentation management)

  • You may also work to Ensure compliance with timely training completion/documentation, Respond to customer inquiries and participate in customer calls/meeting upon Project Manager request, Take the lead in managing various aspects of a project as requested and Work on related projects and tasks as assigned.

What we look for:

  • BS, BA or equivalent 

  • Ability to manage multiple tasks simultaneously

  • Ability to organize and manage multiple priorities with multiple stake holders.

  • Experience dealing with external customers and have a customer service orientation

  • Comfortable operating in a technologically dynamic environment.

  • Willingness to adopt new systems and adhere to established business practices.

  • Knowledge and comfort in using all applications included in the Microsoft Office Product Suite.

  • Healthcare and/or medical experience, preferred. Knowledge of or ability to learn about the drug development process.

  • Strong interest in the application of new technology to the clinical trials process

  • Comfortable working in a fast-paced environment.

  • Excellent Verbal and Written communication skills

At Clario, we put people first, always. We are united and driven by patients, committed to making a difference, and we are always looking for the best talent to help us transform lives.

Required profile

Experience

Industry :
Biotech: Biology + Technology
Spoken language(s):
English
Check out the description to know which languages are mandatory.

Soft Skills

  • Service Orientation
  • Interpersonal Skills
  • Multitasking
  • Teamwork
  • Proactivity

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