Clinical Research Coordinator I

Position Title Clinical Research Coordinator I Department Global Project Delivery Job Type This role is a per-diem contract opportunity* About the Company Ora is a leading full-service ophthalmic drug and device development firm that guides clients across all phases of clinical research to bring new products and therapies to market. The Role Ora’s Clinical Research Coordinator I (CRC I) works closely with study subjects and collaborates with clinical teams across internal and external sites. Responsibilities include on-site study visit support, data collection, protocol compliance, and cross-functional coordination with other coordinators and investigators. What You’ll Do Participate in a 3‑week onboarding program (virtual and in‑person) to master introductory skill sets required for clinic work. Travel to assigned research sites for study visits, performing start‑up activities such as chart preparation and site cleanliness. Maintain study documents including source documentation, case report forms, and regulatory paperwork. Use proprietary technology to perform tasks such as informed consent, medical history documentation, vital sign taking, scribing for medical staff, dispensing study drug, allergy skin testing, and other ophthalmic assessments. Prioritize an exceptional subject experience, ensuring safety and protocol adherence. Collaborate with on‑site staff, including other Ora team members and clinic-based investigators. Screen, recruit, and enroll patients and perform clinical tasks defined in SOPs during study visits. Continue training to advance required clinic skills. Maintain protocol compliance with SOP, ICH‑GCP, and company regulations. Submit timesheets and expenses related to site travel in a timely manner. Enter data into electronic databases and resolve data queries. Travel domestically up to 90% of the time, including back‑to‑back trips and weekends if necessary. Adhere to Ora’s systems and processes to maintain data integrity, business ethics, and regulatory compliance. Demonstrate Ora’s core values: kindness, operational excellence, cultivating joy, and scientific rigor. Responsibilities may vary based on specific business needs. What We Look For Experience Needed for the Role Bachelor’s degree in Life Sciences or 1 year of clinical experience. Additional Skills & Attributes Previous experience as a research coordinator preferred. Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications strongly preferred. Medical certifications such as CPT (phlebotomist technician) or EMT (emergency medical technician) preferred. Flexible schedule with weekend availability and willingness to travel domestically. Team‑player attitude with a strong interest in clinical studies and patient interaction. Competencies and Personal Traits Execution Excellence: set goals, create structure, maintain focus, and collaborate for timely, high‑quality work. IQ, EQ, and SQ: agile, positive thinker and communicator who uses a growth mindset to work and lead with authenticity, transparency, resilience, and empathy. Clear and Direct Communication, Feedback, and Conflict Resolution: practice radical candor and promote psychological safety. Seek meaning and purpose, striving to be part of something larger than oneself. Benefit Eligibility Full‑time employees working a minimum of 30 hours per week are eligible for medical and dental coverage. Per‑diem workers become eligible after 6 months of service and an average of 30 hours per week. Equal Opportunity & Diversity Ora is a proud affirmative action and equal opportunity employer committed to equal employment opportunity and fair, equitable compensation regardless of race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status. We encourage applications from people of color, the LGBTQIA+ community, disabled candidates, and veterans. #J-18808-Ljbffr Ora