Want to hear how I work? Hit play.Find roles with Kablio AI to help build and power the world.Kablio AI helps you secure roles in construction, clean energy, facilities management, engineering, architecture, sustainability, environment and other physical world sectors.
Get hired, get rewarded!
Land a job through Kablio and earn a 5% salary bonus.
Exclusive benefits
5%Bonus
Clinical Research Coordinator
Actalent
An engineering and sciences services and talent solutions firm connecting specialized experts with industry projects.
Manage and coordinate clinical trial protocols, ensuring compliance with institutional guidelines and smooth operation.
Provide regular reports to tumor study group members and the Principal Investigator on assigned studies using Oncore®.
Serve as a liaison with study sponsors, scheduling monitoring visits and conference calls, and addressing sponsors’ queries accurately and promptly.
Coordinate the preparation of study tools, such as study binders, medication diaries, eligibility checklists, and flow sheets using Oncore®, Excel®, and Word.
Assist with grading adverse events using the NCI common toxicity criteria or protocol-specific grading scales and complete Serious/Unexpected Adverse Event forms as required.
Ensure that IRB approved informed consent forms are obtained, signed, and properly filed, with copies provided to patients.
Maintain comprehensive research records for all patients enrolled in studies, including patient consent, eligibility, Case Report Forms, and registration confirmations.
Collaborate with the Research Nurse Clinician and/or physician to review patients’ charts and confirm protocol eligibility, while obtaining necessary source documents.
What you bring
clinical research
bachelor’s degree
oncology experience
blood processing
data management
medidata
4+ years of clinical research experience, including patient recruitment and data management.
Bachelor's Degree minimum.
4+ years of oncology experience.
Blood processing experience.
Strong data management skills, as 60% of the role involves data management and coordination.
Experience working with multiple EDC systems, particularly Medidata and Inform.
Experience in recruiting, screening, and consenting patients for clinical trials.
Experience in gynecological oncology, even if not directly from clinical research settings, is acceptable.
Benefits
Health Spending Account (HSA)
Medical, dental & vision
Life Insurance (Voluntary Life & AD&D for the employee and dependents)
Critical Illness, Accident, and Hospital
Short and long-term disability
Transportation benefits
Employee Assistance Program
401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
Time Off/Leave (PTO, Vacation or Sick Leave)
Training + Development
Information not given or found
Interview process
Information not given or found
Visa Sponsorship
Information not given or found
Security clearance
background checks may be conducted as part of the employment process
Hey there! Before you dive into all the good stuff on our site, let’s talk cookies—the digital kind. We use these little helpers to give you the best experience we can, remember your preferences, and even suggest things you might love. But don’t worry, we only use them with your permission and handle them with care.