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- Tasks: Coordinate exciting clinical research projects and engage with participants to make a difference.
- Company: Join a leading institute focused on innovative eye health research.
- Benefits: Competitive salary, hybrid work model, and opportunities for professional growth.
- Other info: Dynamic role with potential for career advancement in a supportive environment.
- Why this job: Be part of groundbreaking research that impacts vision health and helps communities.
- Qualifications: Bachelor's degree and experience in research coordination or clinical trials preferred.
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. Responsibilities include:
- 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.
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.
Clinical Research Coordinator - Donut in Suffolk employer: Drexel University
Contact Detail:
Drexel University Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Research Coordinator - Donut in Suffolk
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical research field, especially those who might know about opportunities at The Eye Institute. A friendly chat can sometimes lead to a referral, which is gold in the job search game.
✨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’re applying for. We want to see that you’re not just interested but also knowledgeable about the role and its responsibilities.
✨Tip Number 3
Showcase your organisational skills! During interviews, share examples of how you've successfully coordinated projects or managed multiple tasks. This will demonstrate that you can handle the demands of being a Clinical Research Coordinator.
✨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 you’re serious about joining our team at StudySmarter.
We think you need these skills to ace Clinical Research Coordinator - Donut in Suffolk
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Clinical Research Coordinator role. Highlight your relevant experience in clinical trials and project coordination, and don’t forget to mention any specific skills that match the job description.
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about this role and how your background makes you a perfect fit. Be sure to mention your communication skills and experience with research data.
Showcase Your Organisational Skills: Since this role requires excellent planning and organisational skills, make sure to provide examples of how you've successfully managed multiple tasks or projects in the past. We love seeing how you keep everything on track!
Apply Through Our Website: Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the position. Plus, it’s super easy to do!
How to prepare for a job interview at Drexel University
✨Know Your Research Inside Out
Make sure you’re familiar with the specifics of the study, 'Delaying the Onset of Myopia Until Treatment'. Understand its goals, methodology, and significance. This will not only show your genuine interest but also help you answer questions confidently.
✨Showcase Your Coordination Skills
Be ready to discuss your experience in coordinating research projects. Highlight specific examples where you successfully managed recruitment, scheduling, or data entry. This will demonstrate your ability to handle the responsibilities of the Clinical Research Coordinator role.
✨Prepare for Communication Scenarios
Since this role involves liaising between various parties, think of examples where you’ve effectively communicated with different stakeholders. Practice articulating how you would handle potential challenges in communication, especially with participants and institutional review boards.
✨Demonstrate Your Organisational Prowess
Given the need for excellent planning and organisational skills, prepare to discuss how you manage multiple tasks and deadlines. Bring up tools or methods you use to stay organised, as this will reassure them of your capability to thrive in a dynamic environment.