Clinical Research Coordinator - Donut in Eye
Clinical Research Coordinator - Donut

Clinical Research Coordinator - Donut in Eye

Eye Full-Time 47490 - 71230 ÂŁ / year (est.) No home office possible
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At a Glance

  • Tasks: Coordinate clinical trials and engage with study participants to ensure successful research outcomes.
  • Company: Join a leading institute focused on innovative eye care research.
  • Benefits: Competitive salary, hybrid work model, and comprehensive benefits package.
  • Other info: Dynamic role with opportunities for professional growth in a supportive environment.
  • Why this job: Make a difference in eye health while gaining valuable research experience.
  • Qualifications: Bachelor's degree and 3 years of relevant administrative experience required.

The predicted salary is between 47490 - 71230 ÂŁ per year.

This full-time Study Coordinator, working closely with the Principal Investigator (PI) and other study investigators, will coordinate all aspects of an NEI funded trial named “Delaying the Onset of Myopia Until Treatment”. This individual will coordinate research through project recruitment, scheduling and retention of study subjects, and exercising appropriate communication skills when acting as a liaison between the Drexel site, the lead site, and study participants. This individual will conduct data entry, submit materials to the Institutional Review Board, maintain study records, and execute certain administrative tasks. While this is a hybrid role, the majority of on-site work will occur at The Eye Institute and occasional visits to the Drexel University, Elkins Park Campus and Drexel University, University City Campus will be required. Additionally, there will be online study group meetings monthly. This position is grant-funded; employment is contingent upon the continued availability of those funds.

Responsibilities

  • Assist in identifying, recruiting, and obtaining informed consent from eligible participants for research study.
  • Ensure coordination of subjects and study personnel as required by protocol and Good Clinical Practice (GCP) guidelines.
  • Act as liaison between the Drexel Institutional Review Board and external site Institutional Review Boards while utilizing the SMART IRB Reliance System.
  • Encourage and motivate participants to maintain compliance and attendance throughout the study and coordinate all retention aspects.
  • Maintain study records and related documentation as required by protocol and regulatory bodies (internal and external).
  • Work with external study sites and coordinating centers as required.
  • Schedule, participate in, and record minutes for study meetings (in-person and virtually) as required.
  • Maintain the highest level of confidentiality regarding patient and study records.
  • Support and complete all study related paperwork including submissions to the Internal Review Board.
  • Other related duties as assigned.

Required Qualifications

  • Minimum of a Bachelor's Degree in or the equivalent combination of education and work experience.
  • Minimum of 3 years in a similar administrative position.
  • Experience in clinical trials or other health-related programs/research preferred.
  • Demonstrated experience with research and project coordination.
  • Demonstrated experience in research data collection and quality control.
  • Experience with data entry, including knowledge of database, word processing, and spreadsheet applications (e.g., REDCap, MS Word, Excel).
  • Experience maintaining files and keeping research records.
  • Experience preparing and submitting Institutional Review Board documentation such as amendments, continuing reviews, and reportable new information submissions.
  • Excellent written, verbal, and interpersonal communication skills, including tact, diplomacy, and flexibility.
  • Excellent planning, organizational skills, and ability to work in a changing, multiple demand setting.
  • Thorough knowledge of protocol and goals of studies.

Physical Demands

  • Typically sitting at a desk/table.

Location

The Eye Institute - Oak Lane

Additional Information

This position is classified as Exempt, grade J. Compensation for this grade ranges from $47,490 to $71,230 per year. Please note that the offered rate for this position typically aligns with the minimum to midrange of this grade, but it can vary based on the successful candidate’s qualifications and experience, department budget, and an internal equity review. Applicants are encouraged to explore the Professional Staff salary structure and Compensation Guidelines & Policies for more details on Drexel’s compensation framework. For information about benefits, please review Drexel’s Benefits Brochure.

Special Instructions to the Applicant

Please make sure you upload your CV/resume and cover letter when submitting your application. A review of applicants will begin once a suitable candidate pool is identified.

Clinical Research Coordinator - Donut in Eye employer: Drexel University

At The Eye Institute, we pride ourselves on fostering a collaborative and supportive work environment that empowers our Clinical Research Coordinators to thrive. With a strong focus on professional development, employees benefit from ongoing training opportunities and the chance to contribute to groundbreaking research in myopia treatment. Located in Oak Lane, our hybrid work model allows for flexibility while maintaining a strong connection with our team and the broader Drexel University community.
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Contact Detail:

Drexel University Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Research Coordinator - Donut in Eye

✨Tip Number 1

Network like a pro! Reach out to your connections in the clinical research field and let them know you're on the hunt for a Clinical Research Coordinator role. You never know who might have the inside scoop on job openings or can put in a good word for you.

✨Tip Number 2

Prepare for interviews by brushing up on your knowledge of Good Clinical Practice (GCP) guidelines and the specifics of the study you'll be coordinating. Show us that you’re not just a fit on paper, but that you genuinely understand the role and its responsibilities.

✨Tip Number 3

Practice your communication skills! As a Clinical Research Coordinator, you'll need to liaise with various stakeholders. Role-play common interview scenarios with a friend to boost your confidence and ensure you can articulate your thoughts clearly.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows us that you’re serious about joining our team at The Eye Institute.

We think you need these skills to ace Clinical Research Coordinator - Donut in Eye

Project Coordination
Clinical Trials Experience
Data Collection
Quality Control
Data Entry
REDCap
MS Word
Excel
Institutional Review Board Documentation
Communication Skills
Organisational Skills
Confidentiality
Good Clinical Practice (GCP) Guidelines
Participant Recruitment
Retention Strategies

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Clinical Research Coordinator role. Highlight relevant experience in clinical trials and project coordination, as well as any specific skills that match the job description.

Craft a Compelling Cover Letter: Your cover letter should tell us why you're the perfect fit for this position. Use it to showcase your communication skills and your passion for research, while also addressing how you meet the required qualifications.

Showcase Your Organisational Skills: Since this role involves coordinating various aspects of a study, make sure to highlight your organisational skills. Mention any tools or methods you use to keep track of tasks and deadlines, especially in a fast-paced environment.

Apply Through Our Website: We encourage you to apply through our website for a smoother application process. This way, we can easily track your application and ensure it gets the attention it deserves!

How to prepare for a job interview at Drexel University

✨Know Your Research Inside Out

Before the interview, dive deep into the specifics of the study you'll be coordinating. Familiarise yourself with the goals of 'Delaying the Onset of Myopia Until Treatment' and understand the protocols involved. This will not only show your enthusiasm but also help you answer questions confidently.

✨Showcase Your Communication Skills

As a Clinical Research Coordinator, you'll need to liaise with various stakeholders. Prepare examples of how you've effectively communicated in past roles, especially in challenging situations. Highlight your ability to motivate participants and maintain compliance throughout studies.

✨Demonstrate Organisational Prowess

This role requires excellent planning and organisational skills. Be ready to discuss how you've managed multiple tasks or projects simultaneously. Bring up specific tools or methods you use to keep everything on track, especially when it comes to scheduling and maintaining study records.

✨Prepare for Ethical Discussions

Since you'll be working closely with Institutional Review Boards, brush up on ethical guidelines and Good Clinical Practice (GCP). Be prepared to discuss how you would handle sensitive information and ensure confidentiality, as this is crucial in clinical research.

Clinical Research Coordinator - Donut in Eye
Drexel University
Location: Eye

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