Clinical Research Associate

Responsibilities

• Support CRAs with the setup monitoring and closeout of clinical trials in accordance with Good Clinical Practice (GCP) ICH guidelines and company SOPs.
• Assist in site qualification initiation and monitoring visits.
• Review and track clinical trial documentation ensuring accuracy and completeness.
• Collaborate with crossfunctional teams to address studyrelated issues.
• Participate in team meetings and contribute to process improvement initiatives.

Qualifications

• Currently enrolled in a relevant degree program such as list relevant majors e.g. Life Sciences Biology Nursing Public Health
• Strong interest in clinical research and drug development.
• Excellent organizational and time management skills.
• Detailoriented with high standards for accuracy.
• Ability to work independently as well as within a team environment.
• Proficient in Microsoft Office Suite.

What Youll Gain

• Realworld exposure to the clinical research process.
• Mentoring and guidance from experienced CRAs.
• Opportunity to network with industry professionals.
• Potential academic credit (if applicable with your program).
• Potential for future employment opportunities within our company.

Please use the below link for job application and quicker response.

Remote Work :

No