Clinical Research Associate I

WHAT YOU WILL DO

You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.

You will be responsible for (but not only):

• All aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
• All aspects of site management as prescribed in the project plans
• General On-Site Monitoring

Requirements:

• University or college degree, or certification in a related allied health
• profession from an appropriately accredited institution (e.g. nursing licensure)
• 1-3 years of Clinical Monitoring experience

Experience (Minimum Required):

• Six (6) months experience in a related role (e.g., site management, in-house CRA, study coordinator, research nurse, etc.).
• Basic understanding of Regulatory Guidelines.
• Ability to work within a project team.
• Good planning, organization, and problem-solving skills.
• Good computer skills with good working knowledge of a range of computer packages.
• Works efficiently and effectively in a matrix environment.
• Valid Driver's License.