FAQs
What is the job title for this opportunity?
The job title is Clinical Research Assistant.
What are the primary responsibilities of a Clinical Research Assistant?
Primary responsibilities include verifying research study information, inputting data into the EDC system, maintaining research study files, assisting with regulatory documentation, and scheduling subject visits, among other tasks.
What qualifications are required for this position?
A Bachelor’s Degree is required, along with a minimum of 1 year of clinical site experience and at least 6 months of EDC experience.
What is the work schedule for this position?
The work schedule is onsite Monday through Friday from 8:00 AM to 5:00 PM.
Is prior drug trial experience necessary?
Yes, the position requires a minimum of 1 year of clinical site experience, which must include drug trial experience.
Is this position open to applicants from diverse backgrounds?
Yes, Actalent is committed to diversity, equity, and inclusion and considers all applications without regard to race, sex, age, color, or other protected characteristics.
Who can I contact if I need accommodations during the application process?
You can email actalentaccommodation@actalentservices.com for assistance with accommodations during the job application or interview process.
Is this a full-time position?
Yes, this position is a full-time opportunity with a Monday to Friday schedule.
What kind of environment can I expect at Actalent?
Actalent promotes an inclusive environment focused on self-reflection, care, engagement, recognition, and providing growth opportunities for its employees.
Will I be required to perform administrative support functions in this role?
Yes, the role includes various administrative support functions such as office organization and supply management.