FAQs
What are the primary responsibilities of a Clinical Research Assistant?
The primary responsibilities include verifying and correcting research study information, inputting data into the Electronic Data Capture (EDC) system, preparing and maintaining research study files, compiling and submitting study information, assisting with regulatory documentation, and scheduling subject visits.
What qualifications are required for the Clinical Research Assistant position?
Required qualifications include a basic knowledge of clinical trials, in-depth knowledge of departmental and study-specific procedures, and experience with patient recruitment, EDC data entry, and query resolution.
Is experience in clinical trials necessary for this position?
While basic knowledge of clinical trials is required, specific prior experience may not be mandatory; however, familiarity with patient recruitment and data entry is necessary.
What company culture initiatives are emphasized at Actalent?
Actalent emphasizes diversity, equity, and inclusion by hiring diverse talent, maintaining an inclusive environment, fostering a culture of care and engagement, and ensuring growth opportunities for all employees.
Is this position compliant with equal opportunity employment laws?
Yes, the company is an equal opportunity employer and considers all applications without regard to race, sex, age, or any characteristic protected by law.
What should I do if I require accommodations during the application or interview process?
If you need a reasonable accommodation due to a disability, you can email actalentaccommodation@actalentservices.com for assistance with modification or adjustment options.
How does Actalent support career growth for its employees?
Actalent supports career growth through clear growth opportunities, fostering a culture of engagement, and developing skills in a diverse and inclusive environment.
Will I be involved in direct patient interaction as a Clinical Research Assistant?
Yes, you will assist in performing clinical procedures to collect data on patients enrolled in clinical studies, which may involve direct interaction with study subjects.
Is training provided for this role?
Yes, training will be provided to ensure you are familiar with the departmental, protocol, and study-specific operating procedures relevant to your duties.