Clinical Research Associate Manager

Novartis ACC

Singapore

On-site

SGD 120,000 - 170,000

Full time

14 days+
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Job summary

Novartis Singapore seeks a Clinical Research Associate (CRA) Manager & Monitoring Services Oversight Manager to oversee CRA performance, vendor relationships, and ensure quality and compliance of monitoring activities in clinical trials.

The ideal candidate will have 7+ years in clinical research, strong leadership, excellent communication, and the ability to travel internationally. Relocation support is not offered; please apply only if Singapore is accessible.

Qualifications

  • Degree in a scientific or health discipline (advanced degree preferred).
  • 7+ years in clinical research, including planning, execution, and monitoring of clinical trials.
  • Strong project management and team leadership capabilities.
  • Thorough understanding of clinical drug development, GCP/ICH, and health authority regulations.
  • Excellent communication, negotiation, and conflict resolution skills.
  • Ability to travel domestically and internationally.
  • Proficiency with digital and technological tools.

Responsibilities

  • Oversee CRA performance, development, and coaching to ensure delivery, productivity, and quality performance indicators
  • Manage and allocate CRA resources to studies and sites, ensuring balanced workloads and quality monitoring
  • Monitor and approve CRA travel and expenses to ensure compliance with T&E policy and budget
  • Collaborate with SSO Clinical Project Managers to support recruitment strategies and site performance
  • Ensure timely communication with vendors and align resource needs and expectations
  • Oversee vendor monitoring performance targets, including site recruitment commitments, timely data entry, and issue resolution
  • Support clinical development audits, site audits, and inspections, ensuring CAPA follow-up and implementation.

Skills

Project management
Team leadership
Communication
Negotiation
Conflict resolution
Travel ability
Digital literacy/tools

Education

Bachelor's degree in a scientific/health discipline
Advanced degree preferable

Job description

Summary

Internal Role Title: Clinical Research Associate Manager


Location: Singapore


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


About The Role

We are seeking a highly skilled and experienced individual to join our team as a Clinical Research Associate (CRA) Manager & Monitoring Services Oversight Manager. This dual role involves overseeing the performance and development of CRAs, managing vendor relationships, and ensuring the quality and compliance of monitoring activities in clinical trials. The ideal candidate will have a strong background in clinical research, excellent leadership capabilities, and the ability to manage multiple responsibilities effectively.


Key Responsibilities


  • Oversee CRA performance, development, and coaching to ensure delivery, productivity, and quality performance indicators

  • Manage and allocate CRA resources to studies and sites, ensuring balanced workloads and quality monitoring

  • Monitor and approve CRA travel and expenses to ensure compliance with T&E policy and budget

  • Collaborate with SSO Clinical Project Managers to support recruitment strategies and site performance

  • Ensure timely communication with vendors and align resource needs and expectations

  • Oversee vendor monitoring performance targets, including site recruitment commitments, timely data entry, and issue resolution

  • Support clinical development audits, site audits, and inspections, ensuring CAPA follow-up and implementation.


Essential Requirements


  • A degree in a scientific or health discipline; an advanced degree is preferable

  • Minimum 7 years of experience in clinical research, including planning, executing, and monitoring clinical trials

  • Strong project management and team leadership capabilities

  • Thorough understanding of clinical drug development, international standards (GCP/ICH), and health authority regulations

  • Excellent communication, negotiation, and conflict resolution skills

  • Ability to travel domestically and internationally as needed

  • Proficiency in digital and technological tools


Commitment To Diversity & Inclusion

We are 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.


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