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Work Study Creature Design Jobs in Colorado (NOW HIRING)

Design/organize the implementation of clinical research trials and coordinate trials as a Primary ... Must be self-directed with demonstrated ability to work in collaboration and cooperation with ...

Posted today

... studies, and controls system design to meet our clients' expectations and needs. This engineer will be required to travel for approximately 15% of the time. We offer a comfortable, collaborative work ...

Electrical Design Engineer

Fort Collins, CO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

... studies, and controls system design to meet our clients' expectations and needs. This engineer will be required to travel for approximately 15% of the time. We offer a comfortable, collaborative work ...

Transportation Design Engineer

Colorado Springs, CO · On-site

$40.86 - $52.88/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Colorado Springs, CO 80905 or Centennial, CO 80112 💻 Work Arrangement: Hybrid schedule ... Collecting, compiling, and analyzing data from the project site, prior studies, surveys, as-built ...

Transportation Design Engineer

Englewood, CO · On-site

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Colorado Springs, CO 80905 or Centennial, CO 80112 💻 Work Arrangement: Hybrid schedule ... Collecting, compiling, and analyzing data from the project site, prior studies, surveys, as-built ...

Transportation Design Engineer

Centennial, CO · On-site

$40.86 - $52.88/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Colorado Springs, CO 80905 or Centennial, CO 80112 💻 Work Arrangement: Hybrid schedule ... Collecting, compiling, and analyzing data from the project site, prior studies, surveys, as-built ...

Transportation Design Engineer

Centennial, CO · On-site

$85 - $110/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Basis Partners' Design Engineers work under a Senior Design Engineer (Design Lead) in their ... Collecting, compiling, and analyzing data from the project site, prior studies, surveys, as‑built ...

Showing results 21-40

Work Study Creature Design information

What is a work study creature designer?

A Work Study Creature Designer is typically a student or trainee who assists with the creation and conceptualization of creatures for media such as films, video games, or animation as part of a work-study program. Their responsibilities often include sketching, digital modeling, and collaborating with senior designers to develop original creature concepts. This role provides hands-on industry experience while supporting their education and creative portfolio. Work Study Creature Designers gain practical skills in design software, anatomy, and storytelling while contributing to real projects.

How does a work study creature designer typically collaborate with other departments in a creative studio or academic setting?

As a Work Study Creature Designer, you’ll regularly interact with concept artists, animators, writers, and even sound designers to ensure your creature designs fit the overall vision of the project. Collaboration may involve attending team meetings, sharing design drafts for feedback, and making adjustments based on narrative or technical requirements. This role often requires clear communication and adaptability, as you’ll need to balance your creative ideas with the project’s needs and deadlines. By working closely with different departments, you’ll also gain exposure to various stages of production, which can be invaluable for your professional development.

What are the key skills and qualifications needed to thrive as a work study creature designer, and why are they important?

To thrive as a Work Study Creature Designer, you need a strong foundation in art and design principles, anatomy, and a portfolio demonstrating creative character or creature concepts, often supported by formal art education. Proficiency in digital illustration tools such as Adobe Photoshop, ZBrush, or Blender is typically required, and familiarity with 3D modeling or animation software is advantageous. Creativity, attention to detail, and strong collaboration skills help you stand out by bringing unique ideas to life and working effectively with creative teams. These abilities ensure your designs are both imaginative and technically sound, meeting project goals in entertainment, gaming, or film industries.

What is the difference between Work Study Creature Design vs Work Study Character Design?

AspectWork Study Creature DesignWork Study Character Design
Required CredentialsPortfolio, basic art skills, possibly some art coursesPortfolio, character anatomy knowledge, art courses
Work EnvironmentAnimation studios, game development, film productionAnimation studios, game development, film production
Industry UsageDesigning creatures for games, movies, or animationsDesigning characters for similar media

Both roles involve creating visual designs for media projects, but Work Study Creature Design focuses on designing animals and fantastical creatures, while Work Study Character Design centers on human and humanoid characters. The skills, credentials, and work environments are similar, making them closely related but distinct specialties within the entertainment industry.

What are popular job titles related to Work Study Creature Design jobs in Colorado?

For Work Study Creature Design jobs in Colorado, the most frequently searched job titles are:

What job categories do people searching Work Study Creature Design jobs in Colorado look for?

The top searched job categories for Work Study Creature Design jobs in Colorado are:

What cities in Colorado are hiring for Work Study Creature Design jobs?

Cities in Colorado with the most Work Study Creature Design job openings:

Research Study Coordinator

ICON Eyecare

Grand Junction, CO

$27 - $28/hr

Full-time

Posted 7 hours ago

Posted today


Job description

POSITION SUMMARY

EVP Eyecare is a privately held, portfolio company of The Cortec Group. Based in Denver, Colorado, EVP owns and operates a super-regional network of eyecare practices and surgical centers that conduct business under premier brands in Colorado, Texas and Arizona. We believe that delivering on an outstanding patient experience starts with building an outstanding employee experience.

Our mission is to improve people's lives through better vision and outstanding patient experiences.

ESSENTIAL DUTIES AND RESPONSIBILITIES

The essential functions include, but are not limited to the following:

  • Design/organize the implementation of clinical research trials and coordinate trials as a Primary Coordinator.
  • Recruits participants following protocol guidelines and inclusion/exclusion criteria. Communicates with the Investigators regarding enrollment on a frequent basis.
  • Determines effective strategies for retaining participants in clinical trials.
  • Identifies and works to solve problems that may arise while a study is being conducted.
  • Attends professional investigator/coordinator meetings as needed to assure accuracy of protocol implementation and maintain required training.
  • Meets weekly and attends staff meetings to discuss updates.
  • Educates staff members and external partners on protocol requirements.
  • Corresponds and communicates between IRB, PI, and Sponsor to facilitate implementation of protocol.
  • Responsible to notify the Investigators of participant study related serious adverse events, adverse events with trending, safety issues, non-compliance, deviations, Endpoints, and study related charges/billing issues. All reporting will be done with transparency.
  • Facilitates communication between the Investigator and participant regarding the nature of the study, risks, benefits, and alternative treatments to enhance the participants' complete understanding of his rights and responsibilities. Informed consent is to be signed by participant prior to any study related procedures.
  • Evaluates participant's progress while participating in the study via coordinator's assessment and baseline data, history and physical, history, and compliance.
  • Design/Organize a system for each study to accurately maintain records for the study sponsor, IRB and per FDA regulations, if applicable.
  • Complete data entry and other time sensitive tasks to the sponsor or clinical coordinating center per protocol/sponsor timelines.

MINIMUM QUALIFICATIONS (KNOWLEDGE, SKILLS, AND ABILITIES)

  • Bachelor's Degree preferred.
  • Ophthalmic experience and knowledge preferred.
  • Two years (minimum) of related clinical research/industry, managerial, and administrative experience preferred.
    • Combinations of related education and experience may be considered
  • Must be self-directed with demonstrated ability to work in collaboration and cooperation with members of a multidisciplinary team.
  • Ability to effectively communicate and exchange information.
  • Strong organizational and multitasking skills including the ability to manage multiple competing priorities.