Senior Clinical Research Associate

Senior Clinical Research Associate

REQ-10079523
Jun 09, 2026
LOC_CZ

About the Role

Key Responsibilities

  • Lead assigned sites as the primary point of contact throughout study delivery
  • Build strong relationships to ensure site performance, quality, and milestone achievement
  • Manage Phase I to Phase IV trials per monitoring plans and company procedures
  • Conduct site initiation visits and deliver ongoing training for site personnel
  • Perform remote and on-site monitoring to ensure compliance and patient safety
  • Maintain accurate documentation and update all clinical systems in a timely manner
  • Identify risks, resolve issues, and escalate concerns as needed
  • Collaborate with cross-functional teams to drive efficient study execution
  • Support timely data query resolution and ensure data accuracy
  • Act as a subject matter expert across study activities when required

Essential Requirements

  • Minimum of three years of clinical site monitoring experience
  • Minimum of Bachelor’s degree in science, healthcare, or a related field
  • Strong understanding of clinical research and drug development processes
  • Knowledge of ICH/GCP and European regulatory requirements
  • Ability to manage multiple priorities and work independently
  • Strong site management, communication, and problem-solving skills
  • Fluency in written and spoken Czech/Slovak and English
  • Ability to travel extensively, including both domestic and international

Desirable Requirements

  • Experience in radioligand therapy, chimeric antigen receptor T-cell therapy, or oncology

Monthly pension contribution matching your individual contribution up to 3% of your gross monthly base salary; Risk Life Insurance (full cost covered by Novartis); 5-week holiday per year; (1 week above the Labour Law requirement) ; 4 paid sick days within one calendar year in case of absence due to sickness without a medical sickness report; Cafeteria employee benefit program – choice of benefits from Benefit Plus Cafeteria in the amount of 17,500 CZK per year; Meal vouchers in amount of 105 CZK for each working day (full tax covered by company); MultiSport Card; Public Transportation Allowance.

Find out more about Novartis Business Services: https://www.novartis.cz/

Role Requirements

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)

DIV_GD
Research
LOC_CZ
Prague
FCT_RD
Full time
Regular
No
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REQ-10079523

Senior Clinical Research Associate

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Source URL: https://prod1.jobapi.novartis.com.cn/req-10079523-senior-clinical-research-associate

List of links present in page
  1. https://prod1.jobapi.novartis.com.cn/req-10079523-senior-clinical-research-associate
  2. https://www.novartis.cz/
  3. https://www.novartis.com/about/strategy/people-and-culture
  4. https://www.novartis.com/sites/novartis_com/files/novartis-life-handbook.pdf
  5. https://novartis.wd3.myworkdayjobs.com/en-US/Novartis_Careers/job/Prague/Senior-Clinical-Research-Associate_REQ-10079523-1
  6. https://novartis.wd3.myworkdayjobs.com/en-US/Novartis_Careers/job/Prague/Senior-Clinical-Research-Associate_REQ-10079523-1