The Clinical Research Coordinator contributes to the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The position has responsibility for the implementation of research activities for one or more studies. The incumbent recognizes and performs necessary tasks to manage projects and prioritizes work to meet necessary deadlines.

The incumbent is responsible for planning and organizing necessary tasks to ensure adherence to the study protocol and applicable regulations, such as institutional policy and procedures, FDA Code of Federal Regulations (CFR), and ICH Good Clinical Practice (GCP). The Clinical Research Coordinator collaborates with the Principal Investigator (PI), ancillary departments, central research infrastructure teams, sponsors, institutions, and other entities as needed to support the administration of all aspects of studies, including, but not limited to, compliant conduct, financial management, and adequate personnel support.

Required Experience:

1. Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience

2. Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.

3. Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness.

Preferred Experience:

4. Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment.

5. Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.

6. Ability to respond to situations in an appropriate and professional manner