Clinical Research Coordinator I (Bilingual Portuguese; Per Diem)

Andover Eye Institute; Andover (MA); On-site; USD 60,000 - 80,000; Full time

Job summary

A leading eye care institute is seeking a Clinical Research Coordinator I to manage clinical trials. This entry-level role involves collecting and organizing research data, ensuring compliance, and working closely with participants and teams. Candidates should have a Bachelor's degree in Life Sciences and be fluent in Portuguese and English. A commitment to quality and teamwork is essential.

Qualifications

• 1 year experience in a clinical or lab setting including coursework.

Responsibilities

• Collect, record, and organize research information for clinical projects.
• Perform patient screening, recruitment, and enrollment.
• Maintain study documents and ensure compliance with protocols.

Skills

Fluency in Portuguese

Fluency in English

Team player attitude

Education

Bachelor's degree in Life Sciences

Job description

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Andover Eye Institute provided pay range

This range is provided by Andover Eye Institute. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.

Base pay range

$30.00/hr - $35.00/hr

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 (Bilingual) 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:

1. Performs clinical skills identified in the SOP at study visits.
2. Be compliant with SOP, ICH-GCP and regulations.
3. Login time and expenses in a timely manner, follow the guidelines and company expense policy.
4. Participates in study start-up activities such as putting together charts, pulling patient charts, ensuring site cleanliness.
5. Performs patient screening, recruitment, and enrollment.
6. Create study documents as assigned.
7. Maintains study documents, including source documentation, case report forms, and regulatory documentation.
8. Provide Quality Control of documents as required.
9. Adhere to all aspects of Andover Eye Institute quality system.
10. 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.
11. Clear and sustained demonstration of Andover Eye Institute values -- prioritizing kindness, operational excellence, cultivating joy and scientific rigor – as well as their linked behaviors.
12. Responsibilities may differ from the above based on the specific needs of the business.

What We Look For:

● Experience needed for the Role:

• Bachelor's degree in Life Sciences or 1-year experience in a clinical or lab setting including coursework.
• Fluency in Portuguese and English, both written and verbal communication.

● Additional Skills & Attributes:

• Previous experience as a research coordinator is strongly preferred.
• Certified Ophthalmic Associate or Certified Ophthalmic Technician certifications is strongly preferred.
• Advanced degree in related study is preferred but not required.
• Medical skills and/or certifications such as (CPT) certified phlebotomist technician, (EMT) Emergency Medical Technician is 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.

● Competencies and Personal Traits:

o 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.

o How We Do It:

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.

o Why We Do It:

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. Andover Eye Institute 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.

Seniority level

• Entry level

Employment type

• Other

Job function

• Research, Analyst, and Information Technology

Industries

• Research Services

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