FAQs
What are the primary responsibilities of a Clinical Trials Specialist?
The primary responsibilities include supporting Clinical Study Leads in executing global clinical trials, organizing meetings, preparing agendas and minutes, collating data for site selection, reviewing study documents, managing the eTMF, tracking site status, and contributing to departmental initiatives.
What soft skills are important for this role?
Important soft skills for this role include strong organizational skills, attention to detail, effective communication skills, and the ability to manage multiple tasks simultaneously.
Is experience with CROs required for this position?
While prior experience with CROs is beneficial, it may not be strictly required, as the role emphasizes supporting overall execution of clinical trials.
What does the company do to promote diversity, equity, and inclusion?
The company promotes diversity, equity, and inclusion through hiring diverse talent, maintaining an inclusive environment, building a culture of care and recognition, and ensuring growth opportunities for all employees.
What is the company’s policy regarding equal employment opportunities?
The company is an equal opportunity employer and considers all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information, or any characteristic protected by law.
How should I request reasonable accommodations for the application process?
If you need reasonable accommodations due to a disability, you can request them by emailing actalentaccommodation@actalentservices.com for other accommodation options.
Are there opportunities for professional development in this role?
Yes, the company emphasizes growth opportunities for employees, which may include professional development and training programs.
Will the Clinical Trials Specialist need to manage any external vendors?
Yes, part of the role includes managing Third Party Vendors as well as contributing to the overall execution of clinical trials.