Clinical Research Associate I

Responsibilities:

• Provides contextual information on the clinical trials and connects stakeholder to the investigative sites.
• Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program.
• Conducts site evaluation, site training, routine, and site closure monitoring activities under supervision.

Qualifications:

• Appropriate tertiary qualification in health related disciplines preferred or equivalent work experience.
• Clinically related experience, preferably in clinical research coordinating or data management.
• Knowledge on existing and emerging local regulatory and legal requirements, ICH/GCP Guidelines and applicable policies.

Additional Skills:

• Able to work collaboratively and cross functionally to develop and sustain working relationships.
• Demonstrate planning and organizational skills and the ability to work effectively in a dynamic environment.
• Interpersonal skills with strong written, verbal, active listening and presentation skills.