FAQs
What is the main duty of the Clinical Research Coordinator role?
The main duties include chart review and phone screening, with additional responsibilities as needed for the ongoing vaccine clinical trial.
What qualifications are required for this position?
Candidates must have a minimum of one year in a Clinical Research Coordinator role, experience with electronic medical records (EMR), experience with electronic data capture (EDC) systems, and either a bachelor's/associates degree with one year of relevant experience or three years of relevant experience.
Is this position full-time or part-time?
This position is a full-time, onsite role.
What type of experience is preferred for this role?
Clinical research experience is preferred, particularly in areas related to patient recruitment, chart reviews, and phone screenings.
Will there be opportunities for additional duties?
Yes, as the position and study progress, additional job duties may be added that are not listed in the job description.
What is required in terms of intramuscular dose administration?
If applicable and required by state law, the candidate must be able to prepare and administer intramuscular doses.
How can I request accommodations for the application process?
You can request a reasonable accommodation by emailing actalentaccommodation@actalentservices.com for other accommodation options.
What are Actalent’s views on diversity and inclusion?
Actalent values diversity, equity, and inclusion as essential components of their culture and is committed to hiring diverse talent and maintaining an inclusive environment.
Is this a contract position?
Yes, this is a short-term contract position supporting an ongoing vaccine clinical trial.
Are there any specific software systems that I need to be familiar with?
Familiarity with electronic medical records (EMR) and electronic data capture (EDC) systems is required for this role.