[Hiring] Clinical Research Associate (II-SCRA) @Novotech Global

Role Description

The Clinical Research Associate (CRA) is primarily responsible for ensuring the rights and wellbeing of trial participants are protected and the reported trial data are accurate, complete, and verifiable from the source documents. The CRA is the primary contact between the Investigational Sites, Novotech, and Sponsor. Key responsibility of a CRA is as a site relationship manager ensuring that clinical trials are conducted in accordance with ICH GCP guidelines, local and global regulatory requirements, and Novotech/Client SOPs.

• Build relationships with Principal Investigators, study coordinators, pharmacists, and all relevant site trial personnel.
• Foster internal and external customer relationships for efficient project delivery.
• Prepare site essential documents in collaboration with IHCRA and RSA.
• Understand local and international regulatory requirements with RSU Team.
• Drive site recruitment and engagement initiatives.
• Monitor investigational sites as per ICH GCP and Clinical Monitoring Plan.
• Ensure the rights & wellbeing of trial participants are protected.
• Verify trial data accuracy and completeness.
• Ensure proper storage, dispensing, and accounting of study drug.
• Keep the project Trial Master File (TMF) up to date.
• Support sites to be audit and inspection ready.
• Maintain current clinical trial management systems.
• Provide site updates to PM/LCRA as per study requirements.
• Collaborate on-site payments with IHCRA and Site Contract Associates.
• Assist PM with the development of study-related project plans and templates.

Qualifications

• Graduate in a clinical or life sciences-related field.
• Relevant experience/qualifications in allied professions may also be considered.
• Good time management skills and attention to detail.
• Able to work well in a team and be computer literate.
• Experience in the research or pharmaceutical industry preferred.
• CRA II: Approximately 1-2 years of Clinical Research Associate experience or equivalent experience.
• CRA III: At least 2-3 years of Clinical Research Associate experience.
• Sr. CRA: At least 3-5 years of Clinical Research Associate experience.

Requirements

• Salary Band: $70,000 – 140,000 based on candidate's experience level.

Benefits

• Flexible working options.
• Paid parental leave for both parents.
• Flexible leave entitlements.
• Wellness programs.
• Ongoing development programs.

Company Description

Novotech is a global full-service clinical Contract Research Organization (CRO). We are committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect.

• Globally recognized leader in clinical research and scientific advisory services.
• Award-winning workplace culture that values ambition, innovation, and growth.
• Expanded global footprint with 30+ offices across Asia-Pacific, the United States, and Europe.
• Empowers team members to create an effective work-life balance.
• Access to mentorship opportunities and professional development programs.
• Collaborative culture with a commitment to success.