Clinical Research Associate Manager at Novartis

, , Singapore -

Full Time

Start Date

Immediate

Expiry Date

14 Aug, 26

Salary

0.0

Posted On

16 May, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Budget Management, Clinical Research, Clinical Study Reports, Clinical Trials, Clinical Trials Monitoring, Communication, Data Analysis, Decision Making, Health Sciences, Life Science, People Management, Regulatory Compliance

Industry

Pharmaceutical Manufacturing

Description

Band Level 5 Job Description Summary Internal Role Title: Clinical Research Associate Manager Location: Singapore #LI-Hybrid 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. Job Description 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. Skills Desired Budget Management, Clinical Research, Clinical Study Reports, Clinical Trials, Clinical Trials Monitoring, Communication, Data Analysis, Decision Making, Health Sciences, Life Science, People Management, Regulatory Compliance Improving the lives of people living with disease takes more than innovative science. It takes a focus on the needs of people and a community committed to meeting them. It takes a team of people like you. Working together. Learning together. Thriving together. Discover how you can join us in changing people’s lives. Novartis is aware of employment scams which make false use of our company name or leader’s names or recruiter’s names to defraud job seekers. Novartis does not make job offers without interview and never asks candidates for money. If you have encountered a job posting or been approached with a job offer that you suspect may be fraudulent, we strongly recommend you do not respond, send money or personal information. In the context of China Cross-Border Data Transfer (CBDT) policy, if you need to apply for a position in China, please go to the local Recruiting System TaleNov .

Responsibilities

Oversee the performance, development, and resource allocation of Clinical Research Associates to ensure quality monitoring of clinical trials. Manage vendor relationships and ensure compliance with international standards and health authority regulations.