Job Description
We are seeking a highly motivated and organized individual to join our team as a Clinical Research Associate. In this role, you will be responsible for managing study start-up activities from site identification through pre-initiation.
This includes preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDAs), Clinical Site Agreements (CSAs) and any amendments. You will also conduct remote Qualification Visits (QVs) and generate visit/contact reports.
You will work independently with minimal supervision and possess a high level of attention to detail and the ability to prioritize multiple tasks simultaneously.
Key Responsibilities
* Act as direct point of contact with assigned sites, accountable for quality and delivery during the start-up phase.
* Build relationships with investigators and site staff.
* Conduct, drive and manage country specific feasibility and/or site pre-qualification and qualification activities.
* Promptly identify, use judgment and knowledge to address and resolve or escalate any site question and/or issue.
Requirements
* 1-2 years' experience in start up experience is needed.
* Experienced Study Coordinator with start up activities experience from site level considered.