Ora
Ophthalmic drug and device development
ClinicalResearchCoordinator
“Clinical Research Coordinator at Ora. Skills: Clinical research study conduct, Protocol adherence, Subject safety, Data integrity, Regulatory compliance. Conduct world-class research using proprietary methodologies. Administrate technician-based tasks by collecting, recording, and organizing subject and research information during clinical research study visits”
What You'll Achieve.
Bring new products and therapies to market; Efficiently bring new products and therapies to market; Achieve significant positive impact in the wider world
Industry & Context.
Travel to research sites as assigned for study visits, Willing to travel domestically up to 90% of the time including back-to-back trips and weekends, if necessary, Flexible schedule, including weekend availability
What They're Looking For.
Must Have
Bachelor's degree in Life Sciences OR 1-year experience in a clinical setting
Nice to Have
Previous experience as a research coordinator, Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications, Medical skills and/or certifications such as (CPT) certified phlebotomist technician, (EMT) Emergency Medical Technician
What You'll Do.
Conduct world-class research using proprietary methodologies
Administrate technician-based tasks by collecting
and organizing subject and research information during clinical research study visits
Ensure compliance with clinical project protocol and overall clinical objectives
Partner with tenured Clinical Research Coordinators and Clinical Project Managers to execute protocol directives
Work cross-functionally with internal and external teams
Participate in study start-up activities
Maintain study documents
Prioritize and deliver an exceptional subject experience
Collaborate with on-site staff
Perform patient screening
Perform clinical skills identified in the SOP at study visits
Participate in various parallel and compounding trainings
Maintain protocol compliance during clinical projects
Adhere to work instructions and discretion in handling intellectual property
Enter and submit time sheets and expenses
Prompt submission of work availability
Enter data into electronic database and resolves data queries
Adhere to all essential systems and processes that are required at Ora to maintain compliance to Ora’s data integrity & business ethics and regulatory requirements
How You'll Work.
Team & Collaboration
Partner with tenured Clinical Research Coordinators and Clinical Project Managers; Work cross-functionally with internal and external teams such as other Research Coordinators and Investigators; Collaborate with on-site staff, whether they be other Ora team members or clinic-based staff and Investigators; Be a team player
Communication Scope
Clear and Direct Communication; Feedback and Conflict Resolution; Giving and receiving feedback frequently
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