CRA Job at Novotech, Hungary | Apply Now
Looking for a CRA job in Europe? This exciting opportunity at Novotech offers professionals a chance to work at the forefront of clinical research. If you’re passionate about clinical trials, patient safety, and innovative therapies, this role in Hungary could be your next big career move in the life sciences industry.
- Job Position:Â Clinical Research Associate (CRA)
- Location:Â Hungary
About the Company
CRA job seekers exploring global opportunities will find Novotech to be a leading employer in the clinical research space. Novotech is a global full-service clinical Contract Research Organization (CRO). At Novotech, ambition meets opportunity. As a globally recognized leader in clinical research and scientific advisory services, the company combines innovation with an award-winning workplace culture. Since 1997, Novotech has expanded globally with 30+ offices across Asia-Pacific, the United States, and Europe. The organization is recognized as an Employer of Choice and is committed to gender equality and inclusivity. Employees benefit from flexible work options, wellness programs, paid parental leave, and ongoing development opportunities through initiatives like NovoLife.
CRA Job Description
CRA job responsibilities focus on ensuring the rights and wellbeing of trial participants and maintaining accurate clinical trial data. 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. The role also involves ensuring clinical trials comply with ICH GCP guidelines, regulatory requirements, and SOPs.
Qualifications
CRA job eligibility requires a background in life sciences and relevant experience in clinical research.
- Graduate in a clinical or life sciences-related field
- 2–3 years of Clinical Research Associate experience in the clinical industry
- Strong time management and attention to detail
- Ability to work in a team and strong computer skills
- Excellent interpersonal and communication skills
Key Responsibilities – CRA Job
CRA job duties include managing site relationships and ensuring smooth clinical trial operations.
- Build relationships with Principal Investigators, study coordinators, pharmacists, and site personnel
- Ensure efficient and timely project delivery as per study timelines
- Prepare site essential documents and support ethics and regulatory submissions
- Understand local and international regulatory requirements
- Drive participant recruitment and engagement initiatives
- Conduct monitoring visits including site selection, initiation, monitoring, and close-out
- Ensure participant safety, protocol compliance, and adverse event reporting
- Verify accuracy and completeness of trial data and resolve queries
- Ensure proper storage, dispensing, and reconciliation of study drugs
About the Team
CRA job roles at Novotech provide exposure to a collaborative and global work environment. Novotech offers advanced therapeutic and regulatory expertise, enabling employees to work on cutting-edge clinical trials. The company promotes:
- Strategic thinking and proactive decision-making
- A collaborative and inclusive culture
- Strong leadership support
- Opportunities for career growth in a global organization
Work Culture & Benefits
Job professionals at Novotech benefit from a supportive and inclusive workplace. Novotech is committed to diversity, inclusion, and employee wellbeing. The company provides:
- Flexible working options
- Paid parental leave
- Wellness programs
- Professional development opportunities
The organization welcomes individuals from diverse backgrounds, including those with disabilities and caregiving responsibilities.
