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- Tasks: Assist in clinical trials by collecting and organising research data while ensuring compliance.
- Company: Andover Eye Institute is pioneering eye care through innovative clinical trials and research.
- Benefits: Enjoy flexible hours, a supportive team environment, and the chance to make a real impact.
- Why this job: Join a mission-driven team focused on advancing medical breakthroughs and improving patient care.
- Qualifications: Bachelor's degree in Life Sciences or 1-year experience in a clinical setting preferred.
- Other info: Diversity is valued; all backgrounds are encouraged to apply.
The predicted salary is between 28800 - 48000 ÂŁ per year.
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Please note that this role is not for a position at Ora, Inc. This role is for a position at the company Andover Eye Associates, which is a close working partner of Ora, Inc.
POSITION TITLE: Per Diem, Clinical Research Coordinator I
DEPARTMENT: Clinical Studies
LOCATION: On-site, Andover, MA
Revolutionizing clinical trials with unparalleled expertise, patient-focused innovation, and a commitment to delivering results that advance medical breakthroughs
At Andover Eye Institute, our mission is to lead the future of eye care through innovative clinical trials and groundbreaking research. We are committed to advancing the understanding and treatment of ophthalmic conditions by exploring new frontiers in medical science. Our team of experienced and compassionate professionals works closely with participants and sponsors, ensuring that each clinical trial is conducted with the utmost care, precision, and attention to detail.
The Role:
Andover Eye Institute Per Diem, Clinical Research Coordinator I (CRC I) has close relationships with the subjects who participate in our clinical trials. Our CRC I’s will collect, record, and organize research information for clinical projects, while ensuring compliance with clinical project protocol and overall clinical objectives. Our CRC I’s will partner with Clinical Research Coordinators and Clinical Project Managers to execute protocol directives and work cross-functionally with internal and external teams such as other Research Coordinators and Investigators.
What You’ll Do:
- Performs clinical skills identified in the SOP at study visits.
- Maintains protocol compliance during clinical projects.
- Be compliant with SOP, ICH-GCP and regulations.
- Login time and expenses in a timely manner, follow the guidelines and company expense policy.
- Participates in study start-up activities such as putting together charts, pulling patient charts, ensuring site cleanliness.
- Performs patient screening, recruitment, and enrollment.
- Create study documents as assigned.
- Maintains study documents, including source documentation, case report forms, and regulatory documentation.
- Provide Quality Control of documents as required.
- Enters data into electronic database and resolves data queries.
- Adhere to all aspects of Andover Eye Institute quality system.
- Adhere to all essential systems and processes that are required at Andover Eye Institute to maintain compliance to Andover Eye Institute data integrity & business ethics and regulatory requirements.
- Clear and sustained demonstration of Andover Eye Institute values — prioritizing kindness, operational excellence, cultivating joy and scientific rigor – as well as their linked behaviors.
- Responsibilities may differ from the above based on the specific needs of the business.
What We Look For:
- Experience Needed for Role:
- Bachelor\’s degree in Life Sciences or 1-year experience in a clinical or lab setting including course work.
- Previous experience as a research coordinator strongly preferred.
- Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications strongly preferred.
- Advanced degree in related study preferred but not required.
- Medical skills and/or certifications such as (CPT) certified phlebotomist technician, (EMT) Emergency Medical Technician preferred.
- The ability to work a flexible schedule including weekends.
- A team player attitude with a strong interest in clinical studies and enjoy interacting with patients.
- What We Do:
- Execution Excellence: Ability to set goals, create structure and maintain a focused and collaborative approach to the delivery of timely and high-quality work.
- IQ, EQ and SQ: Agile and positive thinker, communicator and collaborator who uses a growth mindset to work and lead with authenticity, transparency, resilience, and empathy. Scientific, intellectual, and emotional/social curiosity creates the willingness and ability to innovate, make mistakes, learn and try again.
- Clear and Direct Communication, Feedback and Conflict Resolution: Practice radical candor in your communication and participate in active Giving and receiving feedback frequently, with an open heart and mind creates psychological safety and promotes faster, individual, team and company growth.
- Seek Meaning and Purpose and a Desire to be Part of Something Bigger than Yourself: Crave being part of a team that works together under shared values to achieve significant positive impact in the wider world.
We know a diverse workforce adds to our collective value and strength as an organization. People of color, the LGBTQIA+ community, disabled candidates and veterans are strongly encouraged to apply. Ora is proud to be an 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.
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Clinical Research Coordinator I employer: Ora
Contact Detail:
Ora Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Coordinator I
✨Tip Number 1
Familiarise yourself with the latest trends and regulations in clinical research, especially those related to ophthalmology. This knowledge will not only help you during interviews but also demonstrate your commitment to the field.
✨Tip Number 2
Network with professionals in the clinical research community, particularly those who work in ophthalmology. Attend relevant conferences or webinars to make connections and learn more about the role and its requirements.
✨Tip Number 3
Prepare to discuss your experience with patient interaction and data management, as these are crucial aspects of the Clinical Research Coordinator role. Think of specific examples that highlight your skills in these areas.
✨Tip Number 4
Showcase your team player attitude by highlighting any collaborative projects you've been involved in. Emphasising your ability to work well with others will align with the values Andover Eye Institute is looking for.
We think you need these skills to ace Clinical Research Coordinator I
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities and requirements of the Clinical Research Coordinator I position. Tailor your application to highlight relevant experiences that align with the job description.
Highlight Relevant Experience: In your CV and cover letter, emphasise any previous experience in clinical settings or research coordination. Mention specific skills or certifications that are preferred for this role, such as being a Certified Ophthalmic Associate or having medical skills.
Craft a Compelling Cover Letter: Write a personalised cover letter that showcases your passion for clinical research and your commitment to patient care. Use examples from your past experiences to demonstrate how you embody the values of Andover Eye Institute.
Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a role that requires compliance and precision.
How to prepare for a job interview at Ora
✨Understand the Role
Make sure you thoroughly understand the responsibilities of a Clinical Research Coordinator I. Familiarise yourself with clinical trial processes, patient interactions, and compliance regulations like SOP and ICH-GCP. This knowledge will help you answer questions confidently.
✨Showcase Relevant Experience
Highlight any previous experience in clinical or lab settings, especially if you've worked as a research coordinator. If you have certifications like Certified Ophthalmic Associate or Technician, be sure to mention them as they are strongly preferred for this role.
✨Demonstrate Team Spirit
Andover Eye Institute values teamwork and collaboration. Be prepared to discuss examples of how you've worked effectively in teams, particularly in clinical settings. Emphasise your ability to communicate clearly and resolve conflicts positively.
✨Align with Company Values
Research Andover Eye Institute's mission and values, such as kindness, operational excellence, and scientific rigor. During the interview, express how your personal values align with theirs and how you can contribute to their goal of advancing eye care through innovative clinical trials.
