Sr. Manager, Clinical Trial Risk Analyst Bristol-Myers Squibb

3.0 - 7.0 years

0 Lacs

hyderabad, telangana

On-site

As a Senior Manager, Clinical Trial Risk Analyst Line Manager at Bristol Myers Squibb, you will play a crucial role in the Clinical Trial Risk Management team under Trial Risk & Integrity Management (TRIM). Your responsibilities will include: - **Overseeing a team of risk monitoring professionals:** You will be responsible for planning, coordinating, and delivering information to support risk evaluation and mitigation, internal decision making, regulatory approval, and market acceptance. You will empower your team to deliver high-quality performance and manage the workload efficiently to avoid delays. - **Managing the book of work:** You will assign resources to studies and initiatives, moni...

Posted 1 month ago

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Centralized Clinical Trial Manager ICON Plc

3.0 - 7.0 years

0 Lacs

karnataka

On-site

As a Centralized Clinical Trial Manager at ICON, you will be responsible for leading the centralized monitoring activities for clinical trials to ensure trial quality and patient safety. Your key responsibilities will include: - Leading the centralized monitoring activities for clinical trials, including data review and risk-based monitoring. - Collaborating with clinical operations, data management, and biostatistics teams to identify potential risks and ensure proactive management of trial data. - Ensuring study compliance with regulatory requirements and protocols by overseeing real-time data reviews and monitoring activities. - Providing oversight on site performance, patient safety, and...

Posted 1 month ago

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Lead Central Monitor Novartis India

5.0 - 9.0 years

0 Lacs

hyderabad, telangana

On-site

Role Overview: As the Lead Central Monitor (Lead CM) at Novartis in Global Clinical Operations (GCO), your primary role is to drive excellence in clinical trial monitoring by establishing and delivering a state-of-the-art Central Monitoring (CM) capability. You will be responsible for managing a team of Central Monitors, developing central and site monitoring strategies, and ensuring that the CM platform configuration aligns with strategic needs and identified indications. Your role is crucial in ensuring appropriate trial data surveillance to deliver quality and integrity of the trials clinical data. Key Responsibilities: - Manage and mentor a team of CMs, fostering professional development...

Posted 2 months ago

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Vice President - Regulatory Compliance HSBC

10.0 - 14.0 years

0 Lacs

maharashtra

On-site

As a VP Regulatory Compliance Advisory for HBAP INM CMB & GBM at HSBC, your role is crucial in ensuring that the operations are effective in identifying, managing, and mitigating Regulatory Compliance and Financial Crime risks. Your responsibilities include: - Supporting CMB & GBM Advisory in maintaining an effective control framework and ensuring compliance with all relevant external laws & regulations, internal codes, and policies with a primary focus on CMB and GBM area. - Articulating the Regulatory Compliance and Financial Crime risks for HBAP INM CMB & GBM. - Providing advisory services to HBAP INM CMB & GBM business to ensure a clear understanding of compliance risk exposure. - Managi...

Posted 2 months ago

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Clinical Operations Manager EY

7.0 - 11.0 years

0 Lacs

karnataka

On-site

At EY, you'll have the chance to build a career as unique as you are, with the global scale, support, inclusive culture, and technology to become the best version of you. And we're counting on your unique voice and perspective to help EY become even better, too. Join us and build an exceptional experience for yourself, and a better working world for all. We are seeking a dynamic Manager to join our Life Sciences Consulting team, specializing in Clinical Operations transformation. This role involves working with global pharmaceutical, biotech, and medtech clients to optimize R&D and clinical delivery models, streamline operations, and implement emerging technologies across clinical developmen...

Posted 3 months ago

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