Clinical Research Project Coordinator II (Pawtucket) in Warwick
Clinical Research Project Coordinator II (Pawtucket)

Clinical Research Project Coordinator II (Pawtucket) in Warwick

Warwick Full-Time 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Oversee clinical research projects and manage daily operations involving human subjects.
  • Company: Care New England, a leader in medical research and innovative healthcare services.
  • Benefits: Competitive salary, inclusive environment, and opportunities for professional growth.
  • Why this job: Make a real difference in healthcare while gaining valuable experience in research.
  • Qualifications: Bachelor's degree and 3-5 years of relevant experience required.
  • Other info: Join a dynamic team dedicated to advancing medical research and improving lives.

The predicted salary is between 36000 - 60000 £ per year.

The Clinical Research Project Coordinator II provides oversight and support in the research and non-clinical administrative aspects of projects involving human subjects. The incumbent implements and oversees the daily operations of the study which include monitoring participant recruitment, implementing protocols, managing research data and samples, and supervising staff. Assists with administrative functions including IRB compliance, maintaining supplies, writing proposals, ensuring compliance with grant criteria, assisting in marketing initiatives, and providing reports. The incumbent maintains data required by sponsors, aids in preparing project-related reports, and serves as a resource to all entities/individuals involved in the specific research study. Additionally, the incumbent assists in preparing and reviewing submissions to sponsors, including budgeting, and/or maintaining and managing project budgets.

Responsibilities

  • Manages research project(s) involving human subjects
  • Trains and supervises project specific staff (Clinical Research Assistants I-III, volunteers, students, consultants, etc); records HR issues as needed
  • Assists in the planning, implementation, and management of project data
  • Promotes the project(s) through marketing, website, other sources, etc.
  • Coordinates project meetings including creating agendas and drafting minutes
  • Collaborates on presentations, publications, and dissemination of project results, as requested
  • Supervises biospecimen collection, packaging, shipping, and infection control procedures
  • Aids in preparation of IRB protocols, amendments, annual reviews, risk assessments, adverse event reports, and informed consent documents; communicates with IRB throughout submission and review process
  • Supports Principal Investigator in preparing regulatory reports, including convening DSMB meetings and writing DSMB reports, and assisting with sponsor progress reports.
  • Helps prepare and review grant submissions, including budgets, according to sponsor guidelines
  • Manages financial functions related to grant and budget compliance
  • Interfaces with grants management office and sponsors

Qualifications and Specifications

  • Bachelor's Degree Required
  • Minimum 3 to 5 Years of Experience
  • CCRP, CCRA, or ACRP-CP preferred
  • Excellent communication skills and analytic abilities
  • Basic computer skills, e.g. familiarity with Microsoft software, completing spreadsheet/data entry
  • Ability to work with diverse populations and support an inclusive, culturally responsive environment

Care New England Health System (CNE) and its member institutions, Butler Hospital, Women & Infants Hospital, Kent Hospital, VNA of Care New England, Integra, The Providence Center, and Care New England Medical Group, and our Wellness Center, are trusted organizations fueling the latest advances in medical research, attracting top specialty-trained doctors, and honing renowned services and innovative programs to engage in the important discussions people need to have about their health.

Americans with Disability Act Statement: External and internal applicants, as well as position incumbents who become disabled must be able to perform the essential job-specific functions either unaided or with the assistance of a reasonable accommodation, to be determined by the organization on a case-by-case basis.

EEOC Statement: Care New England is an equal opportunity employer. All applicants will be considered for employment without attention to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran or disability status.

Ethics Statement: Employee conducts himself/herself consistent with the ethical standards of the organization including, but not limited to hospital policy, mission, vision, and values.

Clinical Research Project Coordinator II (Pawtucket) in Warwick employer: Care New England

Care New England Health System is an exceptional employer that prioritises employee growth and development within a collaborative and inclusive work culture. Located in Pawtucket, our organisation offers comprehensive benefits, including competitive salaries and opportunities for professional advancement, all while contributing to groundbreaking medical research that positively impacts the community. Join us to be part of a team that values innovation, diversity, and the well-being of both our employees and the patients we serve.
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Contact Detail:

Care New England Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Clinical Research Project Coordinator II (Pawtucket) in Warwick

✨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 lookout for opportunities. You never know who might have the inside scoop on a job opening or can put in a good word for you.

✨Tip Number 2

Prepare for interviews by researching the company and its projects. Familiarise yourself with their recent studies and be ready to discuss how your experience aligns with their goals. This shows you're genuinely interested and can hit the ground running!

✨Tip Number 3

Don’t underestimate the power of follow-ups! After an interview, send a quick thank-you email to express your appreciation and reiterate your enthusiasm for the role. It keeps you fresh in their minds and shows your professionalism.

✨Tip Number 4

Apply through our website for the best chance at landing that Clinical Research Project Coordinator II role. We love seeing applications directly from our site, and it helps us keep track of all the amazing talent out there!

We think you need these skills to ace Clinical Research Project Coordinator II (Pawtucket) in Warwick

Project Management
Clinical Research Knowledge
IRB Compliance
Data Management
Budgeting
Analytical Skills
Communication Skills
Staff Supervision
Marketing Initiatives
Report Writing
Biospecimen Handling
Diverse Population Engagement
Regulatory Reporting
Grant Submission Preparation

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Clinical Research Project Coordinator II role. Highlight relevant experience, especially in managing research projects and working with human subjects. We want to see how your skills match what we're looking for!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about clinical research and how your background makes you a great fit for our team. Keep it engaging and personal – we love to see your personality come through!

Showcase Your Communication Skills: Since this role involves a lot of collaboration and reporting, make sure to highlight your communication skills in your application. Whether it's through your writing style or examples of past teamwork, we want to know how you connect with others.

Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands. Plus, it shows us that you’re genuinely interested in joining our team at StudySmarter!

How to prepare for a job interview at Care New England

✨Know Your Research Inside Out

Before the interview, dive deep into the specifics of the research projects you'll be coordinating. Familiarise yourself with the protocols, participant recruitment strategies, and data management processes. This will not only show your enthusiasm but also demonstrate your capability to manage the complexities of the role.

✨Showcase Your Communication Skills

As a Clinical Research Project Coordinator, excellent communication is key. Prepare examples of how you've effectively communicated with diverse teams or stakeholders in past roles. Be ready to discuss how you would handle project meetings, create agendas, and draft minutes to keep everyone on the same page.

✨Highlight Your Compliance Knowledge

Understanding IRB compliance and grant criteria is crucial for this position. Brush up on relevant regulations and be prepared to discuss your experience with preparing IRB protocols, amendments, and risk assessments. This will reassure the interviewers that you can navigate the regulatory landscape smoothly.

✨Demonstrate Your Leadership Abilities

You'll be supervising staff and managing project budgets, so it's important to convey your leadership style. Share specific instances where you've trained or mentored team members, resolved HR issues, or managed financial functions. This will illustrate your readiness to take on the responsibilities of the role.

Clinical Research Project Coordinator II (Pawtucket) in Warwick
Care New England
Location: Warwick
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  • Clinical Research Project Coordinator II (Pawtucket) in Warwick

    Warwick
    Full-Time
    36000 - 60000 £ / year (est.)
  • C

    Care New England

    1000-5000
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