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Hyderabad, Telangana, India Bristol Myers Squibb Full timePosition Summary / Objective : Manage a team that Reconciles and Prepare Clinical Trial Submission documents adhering to regulatory guidelines and ensuring consistency across all BMS programs Position Responsibilities: - Supervisory responsibility for Clinical Trial Support Specialists, providing support of the in house and outsourced studies in support of...
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Hyderabad, Telangana, India Bristol Myers Squibb Full timeManage a team that Reconciles and Prepare Clinical Trial Submission documents adhering to regulatory guidelines and ensuring consistency across all BMS programs- Supervisory responsibility for Clinical Trial Support Specialists, providing support of the in house and outsourced studies in support of CTMS activities to ensure consistency across the team.-...
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Hyderabad, Telangana, India Bristol Myers Squibb Full timeManage a team that Reconciles and Prepare Clinical Trial Submission documents adhering to regulatory guidelines and ensuring consistency across all BMS programsSupervisory responsibility for Clinical Trial Support Specialists, providing support of the in house and outsourced studies in support of CTMS activities to ensure consistency across the team.Oversee...
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Senior Clinical Science Director
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Senior Clinical Trial Support Specialist
2 weeks ago
We are seeking a Senior Clinical Trial Support Specialist to join our team at Bristol Myers Squibb. As a key member of our global clinical operations team, you will be responsible for supporting the regulatory submission process for clinical trials, ensuring compliance with ICH/GCP guidelines and regulatory requirements.
Key Responsibilities:- Support the preparation and submission of regulatory documents for clinical trials
- Collaborate with cross-functional teams to ensure adherence to regulatory requirements
- Prioritize book of work for CTSS team and assign resources based on priority projects
- Develop and maintain relationships with senior-level multifunctional teams across the oncology portfolio
The successful candidate will have a minimum of 5 years of experience in health sciences or a related industry, with supervisory responsibility and experience working with Veeva Vault.
