Clinical Research Coordinator I

About the role

This role is a per-diem contract opportunity at Ora, a leading full-service ophthalmic drug and device development firm. Ora is dedicated to building the future of ophthalmic clinical research through its expert teams and unique methodologies.

Responsibilities

• Travel to research sites as assigned for study visits to prepare for or continue clinical study conduct
• Contribute to and maintain study documents, including source documentation, case report forms, and regulatory documentation
• Perform various tasks such as using proprietary technology, performing the Informed Consent process, documenting medical history and medications, taking vitals, scribing for medical staff, dispensing study drug, performing allergy skin tests, documenting controlled environment stats, and other ophthalmic assessments
• Prioritize and deliver an exceptional subject experience, putting subject safety and protocol adherence to the forefront of your work
• Collaborate with on-site staff, whether they be other Ora team members or clinic-based staff and Investigators
• Perform patient screening, recruitment, and enrollment
• Participate in various parallel and compounding trainings to continue advancement of required clinic skills
• Maintain protocol compliance during clinical projects and adherence to work instructions and discretion in handling intellectual property
• Enter and submit time sheets and expenses related to site travel in a timely manner, following the company expense policy
• Enter data into electronic database and resolve data queries

Requirements

Previous experience as a research coordinator is strongly preferred. A Bachelor's degree in Life Sciences or 1-year experience in a clinical setting is also required. Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications are strongly preferred, along with medical skills and/or certifications such as CPT certified phlebotomist technician or EMT Emergency Medical Technician.

Qualifications

• A team player attitude with a strong interest in clinical studies and enjoy interacting with patients
• A flexible schedule, including weekend availability, and the ability to travel domestically as needed
• Clear and sustained demonstration of Ora’s values -- prioritizing kindness, operational excellence, cultivating joy and scientific rigor – as well as their linked behaviors

Skills

Strong organizational and interpersonal skills, attention to detail, and the ability to prioritize tasks effectively are essential. Proficiency with electronic databases and compliance with clinical protocols are also required.

Benefits

Full-time employees of Ora working a minimum of 30 hours per week are eligible for Medical and Dental coverage after 6 months of service and working an average of 30 hours per week. Per diem workforce is eligible for benefits upon meeting eligibility criteria.

Pay

Compensation details are not specified in this posting.

Schedule

The role requires a flexible schedule, including weekend availability, and the ability to travel domestically as needed. Adherence to all essential systems and processes is required to maintain compliance with Ora’s data integrity & business ethics and regulatory requirements.