English
French
Spanish
Clinical Research Associate (All levels)
Chicago, IL, US
Scientific
Bachelors Degree
Full Time, Temporary
Experienced (Non-Manager)
Remote
Biotechnology/Pharmaceuticals
First Shift (Day)
Chicago, IL, US
Experienced (Non-Manager)
Full Time, Temporary
Biotechnology/Pharmaceuticals
Remote
Scientific
Bachelors Degree
First Shift (Day)
Job details
Clinical Research Associate (CRA) (all levels)
Are you a passionate and dedicated Clinical Research professional looking to make a significant impact in the field of medical science? Join our client’s dynamic team as a Clinical Research Associate (CRA) and contribute to groundbreaking research based in either Chicago or Boston.
Job Specifications:
- Job Type: Full-Time
- Location: Remote, based in Chicago or Boston
- Pay Rate: Based on experience, Starting at $100,000
- Travel: Up tp 80%
Job Summary:
As a Clinical Research Associate (CRA), you will play a crucial role in the planning, execution, and monitoring of clinical trials. You will ensure compliance with regulatory requirements, maintain high standards of data integrity, and work closely with investigative sites to facilitate successful study outcomes.
Roles and Responsibilities:
- Monitor clinical trials to ensure compliance with the protocol, regulatory requirements, and good clinical practice (GCP).
- Conduct site visits, including pre-study, initiation, routine monitoring, and close-out visits.
- Review and verify case report forms and other clinical data for accuracy and completeness.
- Ensure proper documentation and reporting of adverse events.
- Collaborate with clinical investigators and site staff to resolve issues and ensure timely data collection and reporting.
- Prepare and present detailed monitoring reports.
- Assist in the development and review of study-related documents, including protocols and informed consent forms.
- Maintain up-to-date knowledge of regulatory requirements and industry best practices.
Qualifications & Skills:
- Bachelor’s degree in a related field (life sciences, nursing, pharmacy, etc.).
- Minimum of 2 years of experience in clinical research or related field.
- Strong knowledge of GCP, ICH guidelines, and FDA regulations.
- Excellent organizational and communication skills.
- Ability to work independently and manage multiple priorities.
- Proficiency in Microsoft Office Suite and clinical trial management systems (CTMS).
Opportunities:
- Career advancement within a rapidly growing organization.
- Professional development and continuous learning opportunities.
- Participation in high-impact clinical trials and innovative research projects.
- Networking with industry leaders and experts.
9687792
I want more jobs like this in my inbox.
Similar Jobs
Why Kelly® Science & Clinical?
Kelly Science & Clinical is your connection to premier scientific and clinical companies looking to hire industry experts just like you. Our team creates expert talent solutions to solve the world’s most critical challenges. Every day, we match science professionals with dream jobs that fit their skills, interests, and career goals—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background and education in science, so we know a thing or two about the science market and how to get your expertise noticed.About Kelly
Work changes everything. And at Kelly, we’re obsessed with where it can take you. To us, it’s about more than simply accepting your next job opportunity. It’s the fuel that powers every next step of your life. It’s the ripple effect that changes and improves everything for your family, your community, and the world. Which is why, here at Kelly, we are dedicated to providing you with limitless opportunities to enrich your life—just ask the 300,000 people we employ each year.Kelly Services is proud to be an Equal Employment Opportunity and Affirmative Action employer. We welcome, value, and embrace diversity at all levels and are committed to building a team that is inclusive of a variety of backgrounds, communities, perspectives, and abilities. At Kelly, we believe that the more inclusive we are, the better services we can provide. Requests for accommodation related to our application process can be directed to Kelly’s Human Resource Knowledge Center. Kelly complies with the requirements of California’s state and local Fair Chance laws. A conviction does not automatically bar individuals from employment. Kelly participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S.