- Reporting of adverse events in accordance with regulatory requirements
- Data entry into electronic systems
- Administrative tasks including document management and correspondence
- Clinical research experience (1-2 years)
- Able to work independently as well as part of a team
Part-TimeClinicalResearchCoordinators - Birmingham - beBeeClinicalResearch
Job title: Part-Time Clinical Research Coordinator — Independent Impact
Description
We are seeking a highly skilled and motivated Clinical Research Coordinator to join our team on a part-time basis.
About the Role
This is an exciting opportunity for individuals with 1-2 years of clinical research experience to take their career to the next level. As a Clinical Research Coordinator, you will be responsible for reporting adverse events, data entry, and administrative tasks.
Responsibilities:
In this role, you will have the opportunity to work closely with our experienced team members while also developing your skills in clinical research coordination. If you are passionate about delivering high-quality results and making a meaningful impact in the field of clinical research, we encourage you to apply.
Your Skills and Qualifications
We offer competitive benefits that support your health and wellbeing. Apply now if you would like more information about these opportunities!