Description
We are seeking a Clinical Research Assistant to support our clinical research team. As a Clinical Research Assistant, you will play a crucial role in ensuring the smooth operation of clinical trials.
Responsibilities:
- Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems
- Prepare, handle, distribute, file, and archive clinical documentation and reports
- Review study files for completeness
- Assist with preparation, handling, and distribution of Clinical Trial Supplies
- Track and manage Case Report Forms (CRFs), queries, and clinical data flow
- Act as a central contact for the clinical team for designated project communications
- May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training
Qualifications:
- Bachelor's Degree Required
- 3 years administrative support experience
- Equivalent combination of education, training, and experience
- Computer skills including working knowledge of Microsoft Word, Excel, and PowerPoint
- Written and verbal communication skills including good command of English language
- Effective time management and organizational skills
- Ability to establish and maintain effective working relationships with coworkers, managers, and clients
- Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
- Knowledge of applicable protocol requirements
Benefits:
- Competitive salary: $35,800.00 - $123,000.00 per year
- Incentive plans, bonuses, and/or other forms of compensation may be offered
- A range of health and welfare and/or other benefits