FAQs
Is this position remote or on-site?
This is a fully on-site position in Madison, Wisconsin.
What are the working hours for this position?
Shifts are available for 1st (7:00 AM to 3:00 PM CST) and 2nd (3:00 PM to 11:00 PM CST).
What responsibilities will a Clinical Trial Assistant I Dietary have?
Responsibilities include food preparation and dietary requirements as per clinical trial protocols, maintaining clinical study documentation, processing Data Collection Forms, assisting in quality control audits, coordinating Investigator payments, producing presentation materials, and tracking team member activities.
What hard skills are required for this position?
Required hard skills include knowledge in healthcare, clinical research, and dietary management.
Is previous experience in clinical research necessary for this position?
While previous experience in clinical research can be beneficial, specific requirements regarding experience may vary, and candidates are encouraged to apply if they meet the other qualifications.
What is Actalent's stance on diversity, equity, and inclusion?
Actalent is committed to diversity and inclusion, which are embedded into their culture through hiring diverse talent, maintaining an inclusive environment, building a culture of care and engagement, and ensuring growth opportunities for all employees.
How can someone request accommodations during the application or interview process?
Individuals can request a reasonable accommodation by emailing actalentaccommodation@actalentservices.com for other accommodation options.
What type of training will be provided for this role?
The Clinical Trial Assistant I Dietary will receive cross-training on other research tech activities in addition to their primary responsibilities.