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About the Role
Novotech is a global full-service clinical Contract Research Organization (CRO) seeking passionate individuals to advance therapies that improve patient outcomes worldwide. We offer a dynamic environment where ambition meets opportunity, fostering innovation and growth.
Responsibilities
- Build relationships with Principal Investigators, study co-ordinators, pharmacists, and relevant site trial personnel to ensure efficient trial management.
- Foster internal and external customer relationships to ensure focus on efficient, timely, and productive project delivery.
- Prepare site essential documents and support ethics and regulatory submission processes.
- Understand applicable local and international regulatory requirements for specific clinical trials.
- Monitor investigational sites according to ICH GCP and the Clinical Monitoring Plan, including all visit types (selection, initiation, monitoring, close-out, pharmacy visits) either onsite or remotely.
Requirements
- Graduate in a clinical or life sciences-related field. Relevant experience/qualifications in allied professions may also be considered.
- Good time management skills.
- Attention to detail.
- Ability to work well in a team.
- Computer literacy.
- CRA II: Approximately 1-2 years of Clinical Research Associate experience or equivalent experience in other roles in the Clinical industry.
- CRA III: At least 2-3 years of Clinical Research Associate experience in the Clinical industry.
Skills
- Clinical trial management
- Customer relationship management
- Regulatory submissions
- ICH GCP
- Clinical monitoring
Experience Level
- CRA II: 1-2 years
- CRA III: 2-3 years
Education Level
- Graduate in a clinical or life sciences-related field
Benefits
- Flexible working options
- Paid parental leave for both parents
- Flexible leave entitlements
- Wellness programs
- Ongoing development programs
- NovoLife flexible benefits framework
About the Company
- Novotech is a global full-service clinical Contract Research Organization (CRO).
- We are a globally recognized leader in clinical research and scientific advisory services.
- Named Employer of Choice, Great Place to Work and Employer of Choice for Gender Equality (EOCGE).
- Expanded global footprint with 30+ offices across Asia-Pacific, the United States, and Europe.
- We have advanced therapeutic and regulatory expertise, the ability to execute across markets and a client-centric service model.
- We foster a culture that values partnership and collaboration, where every voice is heard and valued.
Equal Opportunity
- Committed to being an employer of choice for gender equality and providing an inclusive work environment where everyone is treated fairly and with respect.
- Looking for people who identify as LGBTIQ+, have a disability or have caring responsibilities.
- We are a Circle Back Initiative Employer and commit to respond to every application.