Sr. Manager, Clinical Trial Risk Analyst

3 - 7 years

0 Lacs

Posted:4 days ago| Platform: Shine logo

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Work Mode

On-site

Job Type

Full Time

Job Description

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, monitor workloads, and forecast future resource needs based on the workload. Additionally, you will provide effective coaching and mentoring to ensure consistently high levels of performance and productivity. - **Collaborating with cross-functional teams:** You will work closely with Data Management Lead, Statistician, Global Trial Lead, Quality Lead, Clinical Trial Physician, Clinical Scientist, and other study team members to set up key risk indicators, data quality assessments, and quality tolerance limits. You will also lead risk discussions within the study team and update the risk management plan accordingly. - **Developing and promoting a workplace culture:** You will create an atmosphere that values diversity of thought, promotes integrity, and fosters accountability. Additionally, you will contribute to the development and maintenance of metrics that inform the evaluation of risk monitoring performance and effectiveness. Qualifications required for this role include: - A minimum of a bachelor's degree in Life Sciences (preferred), Analytics, Data Science, Statistics, or Business. - At least 5 years of experience in the pharmaceutical industry with a sound understanding of drug development and 3 years of experience in clinical trial operations. - Expertise in Risk-Based Monitoring principles and relevant tools, technical data analysis, and interpretation. - Advanced leadership skills with the ability to influence and manage key internal stakeholders. - Excellent communication, collaboration, and teamwork skills. - In-depth understanding of GCP, compliance, and regulatory expectations. If you are looking for a challenging, meaningful, and life-changing opportunity in the pharmaceutical industry, this role at Bristol Myers Squibb could be the perfect fit for you. Apply now and take your career to new heights!,

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