Search by job, company or skills

novartis singapore

Clinical Research Associate/ Senior Clinical Research Associate

2-4 Years
Save
new job description bg glownew job description bg glownew job description bg svg
  • Posted 17 hours ago
  • Be among the first 10 applicants
Early Applicant

Job Description

Summary

Location: Singapore

Novartis is unable to offer relocation support for this role: please only apply if this location is accessible for you.

Are you passionate about advancing clinical research and making a real impact on patients lives Join our dynamic team in Singapore as a Clinical Research Associate (CRA), where you'll be at the forefront of innovative clinical trials across Phases I–IV.

Site relationship management role to ensure sustainable trial execution at Site. Performs on-site and remote monitoring activities related to initiation, conduct and timely completion of Phase I-IV GDD trials within the country in adherence with monitoring procedures and processes in accordance with ICH/GCP, local regulations and SOPs. Proactive site performance management (recruitment & quality) and early identification of real site needs and issues as the single best point of contact (internally & externally) for all sites.

About The Role

Key Responsibilities:

  • Act as the primary liaison between Novartis and study sites, ensuring successful collaboration and milestone delivery.
  • Conduct Phase I–IV site monitoring activities (onsite and remote) in compliance with protocols, ICH/GCP, and regulatory standards.
  • Lead Site Initiation Visits and ongoing training for site personnel, including amendments and onboarding.
  • Identify and mitigate site process risks, promoting continuous improvement and compliance culture.
  • Build strong partnerships with sites to enhance patient recruitment and reduce operational issues.
  • Collaborate early with sites on patient inventory and flow to optimize trial readiness.
  • Support audit and inspection readiness, ensuring timely implementation of corrective actions.
  • Work closely with internal stakeholders to resolve data queries and maintain accurate documentation.

Essential Requirements

  • Minimum 2 years of experience in the pharmaceutical industry or related field; monitoring experience preferred.
  • Strong adaptability and ability to influence site partners in a dynamic environment.
  • Excellent communication and relationship-building skills.
  • Proven ability to work independently and manage multiple sites.
  • Analytical thinking and proactive problem-solving capabilities.
  • Willingness to travel. Ability to travel domestically (and possibly internationally) as needed to study sites and for training and meetings.

Commitment To Diversity And Inclusion / EEO Paragraph

Novartis is committed to building an outstanding, inclusive work environment and diverse teams

representative of the patients and communities we serve.

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)

More Info

Job Type:
Industry:
Employment Type:

About Company

Job ID: 147329197

Similar Jobs

Singapore

Skills:

clinical monitoringSite ManagementData ReviewRegistry AdministrationProject CoordinationComputer Skills