FAQs
What is the primary role of a Clinical Trials Specialist?
The primary role of a Clinical Trials Specialist is to support Clinical Study Leads in the execution of global clinical trials, including scheduling meetings, preparing materials, and managing various aspects of study management.
What are some key responsibilities of the Clinical Trials Specialist?
Key responsibilities include coordinating meetings, preparing agendas, collating data for feasibility assessments, reviewing study documents, managing the eTMF, tracking site activation, and monitoring investigator/site status.
What soft skills are important for this position?
Important soft skills for the Clinical Trials Specialist position include strong organizational skills, attention to detail, effective communication skills, and the ability to manage multiple tasks simultaneously.
Does Actalent promote diversity and inclusion in the workplace?
Yes, Actalent promotes diversity and inclusion as a bridge towards equity and success, ensuring that diverse talent is hired and maintaining an inclusive environment through self-reflection and engagement initiatives.
Is this position an equal opportunity role?
Yes, the company is an equal opportunity employer and considers all applications without regard to various protected characteristics.
What type of studies will the Clinical Trials Specialist be involved in?
The Clinical Trials Specialist will be involved in both internally sourced studies and those outsourced to CROs (Contract Research Organizations).
What kind of support is provided during the application process?
Applicants can request reasonable accommodations for the application or interview process due to a disability by emailing actalentaccommodation@actalentservices.com for further options.