Let’s get started
By clicking ‘Next’, I agree to the Terms of Service
and Privacy Policy
Jobs / Job page
Bilingual Clinical Research Coordinator I image - Rise Careers
Job details

Bilingual Clinical Research Coordinator I

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, Bilingual 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 (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:

  • 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.
    • Fluency in Spanish and English, both written and verbal communication.
  • Additional Skills and Attributes:
    • 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.
  • Competencies and Personal Traits:
    • 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.
    • 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.
      • 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.
    • 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. 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.

Our Privacy Policy | Ora (oraclinical.com)

Average salary estimate

$50000 / YEARLY (est.)
min
max
$40000K
$60000K

If an employer mentions a salary or salary range on their job, we display it as an "Employer Estimate". If a job has no salary data, Rise displays an estimate if available.

What You Should Know About Bilingual Clinical Research Coordinator I, Ora

At Andover Eye Associates, we're excited to expand our team with a Bilingual Clinical Research Coordinator I! This role is pivotal as we seek to advance medical breakthroughs through innovative clinical trials. As our Clinical Research Coordinator I, you will serve as a key point of connection between our dedicated research team and our participants. You'll perform various clinical skills during study visits while ensuring strict adherence to study protocols. This isn't just about data collection; it’s about nurturing relationships with patients while collecting and organizing critical research information. We're looking for someone who thrives in a collaborative environment, possessing the ability to smoothly work with Clinical Research Coordinators and Project Managers alike. Your participation will include everything from patient screening and recruitment to data entry and quality control of study documents. It’s a great opportunity to dive deep into the heart of clinical research and make a significant impact in the field of eye care. If you’re fluent in both Spanish and English and hold a Bachelor's degree in Life Sciences or have experience in a clinical or lab setting, we would love to hear from you! Join us in our mission at Andover Eye Associates to transform lives through the power of research.

Frequently Asked Questions (FAQs) for Bilingual Clinical Research Coordinator I Role at Ora
What are the main responsibilities of a Bilingual Clinical Research Coordinator I at Andover Eye Associates?

As a Bilingual Clinical Research Coordinator I at Andover Eye Associates, your main responsibilities will include performing clinical skills at study visits, ensuring protocol compliance throughout clinical projects, and actively participating in tasks such as patient recruitment and enrollment. Additionally, you'll collect and organize research data, maintain regulatory documentation, and collaborate with other research team members to ensure the smooth execution of clinical trials.

Join Rise to see the full answer
What qualifications do I need to apply for the Bilingual Clinical Research Coordinator I position at Andover Eye Associates?

To apply for the Bilingual Clinical Research Coordinator I position at Andover Eye Associates, you should have a Bachelor's degree in Life Sciences or equivalent experience of at least one year in a clinical or lab setting. Fluency in both Spanish and English, along with proficiency in clinical research protocols and ethics, is essential. Previous research coordination experience and relevant medical certifications are strongly preferred.

Join Rise to see the full answer
How does the role of a Bilingual Clinical Research Coordinator I contribute to clinical studies at Andover Eye Associates?

The role of a Bilingual Clinical Research Coordinator I is vital to the success of clinical studies at Andover Eye Associates. By acting as a liaison between participants and the research team, you help to foster trust and understanding, ensuring a smoother study process. Your expertise in gathering and managing research data supports the overall clinical objectives, ultimately leading to valuable insights in ophthalmic research.

Join Rise to see the full answer
What skills are essential for success as a Bilingual Clinical Research Coordinator I at Andover Eye Associates?

Successful Bilingual Clinical Research Coordinators I at Andover Eye Associates possess several essential skills, including strong communication abilities in both English and Spanish, exemplary organizational skills, and a keen attention to detail. Additionally, being a team player with a passion for clinical studies and a commitment to ethical practice will benefit you in this role.

Join Rise to see the full answer
What does the team culture look like for Bilingual Clinical Research Coordinator I at Andover Eye Associates?

At Andover Eye Associates, the team culture for Bilingual Clinical Research Coordinators I emphasizes collaboration, kindness, and a shared commitment to advancing eye care. We foster an environment where open communication is encouraged, and team members are valued for their contributions. Our collective goal is to positively impact the lives of our participants through innovative clinical research.

Join Rise to see the full answer
Common Interview Questions for Bilingual Clinical Research Coordinator I
Can you describe your experience as a Clinical Research Coordinator?

In answering this question, be specific about your previous roles and responsibilities relevant to clinical research. Mention specific studies you've coordinated, your involvement in patient recruitment and data management, and how you ensured compliance with protocols.

Join Rise to see the full answer
How do you ensure compliance with clinical project protocols?

Emphasize your methods for maintaining compliance, such as regular training, staying updated on regulations, and proactive communication with both the study team and participants. Mention any tools or systems you've used to track compliance.

Join Rise to see the full answer
What strategies do you use to effectively recruit participants for clinical trials?

Discuss your understanding of the target population, your experience utilizing various recruitment channels, and your skills in building rapport with potential participants. Personal stories or examples can enhance your response.

Join Rise to see the full answer
How would you handle a situation where a participant is not adhering to the study protocol?

Showcase your problem-solving skills by discussing your approach to addressing non-compliance—such as open communication with the participant to understand their perspective, providing reminders about study requirements, and documenting the situation appropriately.

Join Rise to see the full answer
What role does communication play in your work as a Clinical Research Coordinator?

Highlight the importance of clear and direct communication with team members, participants, and sponsors. Share examples where effective communication has resolved issues or improved study outcomes.

Join Rise to see the full answer
How do you manage your time and prioritize tasks during a clinical study?

Discuss your organizational skills and any time management techniques or tools you employ. Explain how you prioritize tasks based on urgency and importance, and ensure that all study milestones are met on schedule.

Join Rise to see the full answer
What do you know about the ethical guidelines in clinical research?

Defining key ethical principles such as informed consent, confidentiality, and data integrity is essential. Discuss your familiarity with regulatory guidelines and the importance of ethical considerations in ensuring participant safety and study integrity.

Join Rise to see the full answer
Why are you interested in working with Andover Eye Associates?

Express your enthusiasm for the mission of Andover Eye Associates in advancing eye care through research. Relate personal reasons or experiences that align with the organization’s goals and emphasize your desire to contribute to meaningful work.

Join Rise to see the full answer
How do you deal with cross-functional teams during a clinical trial?

Show your collaborative skills by discussing previous experiences working with cross-functional teams. Emphasize your ability to build relationships, share information, and facilitate communication to ensure everyone is aligned.

Join Rise to see the full answer
What qualities do you believe make an effective Clinical Research Coordinator?

Identify key qualities such as attention to detail, empathy towards participants, organizational prowess, and the ability to communicate effectively with diverse groups. Provide examples from your experience that demonstrate these qualities.

Join Rise to see the full answer
Similar Jobs
Photo of the Rise User
NielsenIQ Remote Soseaua Pipera 42 Sector 2 5th and 7th floor, Bucharest, Romania
Posted 7 days ago
Photo of the Rise User
P2P. org Remote No location specified
Posted 4 days ago
Photo of the Rise User
Posted 5 days ago
Photo of the Rise User
Posted 5 days ago
Photo of the Rise User
Posted 9 days ago

O'Reilly provides technology and business training, knowledge, and insight to help companies succeed. Our unique network of experts and innovators share their knowledge and expertise through the company's SaaS-based training and learning solution,...

8 jobs
MATCH
Calculating your matching score...
FUNDING
SENIORITY LEVEL REQUIREMENT
TEAM SIZE
EMPLOYMENT TYPE
Part-time, on-site
DATE POSTED
January 14, 2025

Subscribe to Rise newsletter

Risa star 🔮 Hi, I'm Risa! Your AI
Career Copilot
Want to see a list of jobs tailored to
you, just ask me below!