Scientific Advisor

3 weeks ago

กรงเทพมหานคร, Thailand Bristol Myers Squibb Full time

**Working with Us**
Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.

**Key responsibility of Scientific Advisor**:
**A. External / Field Activities**:
1. Scientific Exchange with Thought Leaders
- Develop and maintain contacts with Thought Leaders, in accordance with the strategy developed by Global Medical to further understand and gain both insight and/or input into treatment patterns, unmet medical needs, patient needs and behaviors, including (1) the scientific activities taking place within the Disease Area and (2) the needs and treatment patterns of healthcare providers.
- Ensure appropriate response to unsolicited scientific questions or requests posed by healthcare providers for approved Products/Brands (in and off label), and for products in development, by providing accurate scientific data in compliance with Company Policies, and legal and ethical standards.
- Contribute to involvement of Thought Leaders, as required and as appropriate, in BMS sponsored studies and other scientific activities.

2. Collect and communicate Field Medical Insights (FMI)
- The SA should profile the medical landscape within the Disease Area and continuously update this knowledge, including expertise in products, patient treatment trends, unmet medical needs, clinical trials and scientific activities.
- Ensure awareness of current Key Insight Topics and Questions and proactively contribute insights gained from healthcare provider interactions to the relevant internal stakeholders, both locally and at the Worldwide level. For BMS Internal Use Only.

3. Provide Medical Services to External Customers
- Liaise appropriately and effectively with the Medical Information department that services the local market, to develop a systematic follow up interaction plan with Health Care Providers, in order to ensure customer satisfaction with the information received in response to their unsolicited scientific questions or requests; and is prepared to discuss these responses and/or expand on the content upon the HCP’s request.
- Fully prepares BMS-contracted speakers, by acting as a facilitator during formal Speaker Training meetings, and/or through regular one-to-one education, ensuring speakers are skilled on the latest approved resources.
- Evaluates a sample of the promotional speakers throughout the year, and provides constructive feedback to speakers regarding accuracy and delivery of scientific data and adherence to the Company Compliance Policies.

4. Provide Clinical Trial Support Clinical Trial/Survey Identification, Planning and Execution
- Lead the identification of potential opportunities for country participation in clinical development programs, by early mapping of centers of excellence, treatment trends and recruitment potential. - Contribute to the ‘early prioritization’ of development programs for the country by integrating data on disease incidence / prevalence, treatment patterns, unmet medical needs and interest from the scientific community.
- Participate actively in providing input to the RCO Hub management on trial and survey feasibility and site suitability.
- Work with RCO Hub to review local/regional protocols, set local recruitment targets and contribute to site selection. - Facilitate clinical trial activities between BMS and investigators for both BMS sponsored (interventional and non-interventional) and BMS supported Investigator Sponsored Researches (in accordance with the appropriate policies and SOPs).
- Provides support to the Clinical Site Manager for site support activities relating to the conduct of a BMS initiated clinical trial For BMS Internal Use Only Pharmacovigilance (depending on local Pharmacovigilance organization in place)
- Ensure that BMS Pharmacovigilance SOPs are understood and applied by Investigators of local studies, and alert appropriate BMS personnel to any Adverse Events that are identified.
- Appropriately provide Medical Service to customers when SAEs and unexpected AEs arise, always keeping the needs of the patient paramount.
- Contribute to ensuring the highest standards of clinical safety - Respond to product related emergency calls, as appropriate.

**B. Internal / Medical Strategy Activities**:

- Country Medical Strategy Key Contributors
- Medical support for internal stakeholders Support & Trainer
- Compliance

**Uniquely Interesting Work, Life-changing Careers**

**On-site Protocol**
Physical presence at the BMS worksite or

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