Scientific Advisor Cardiology

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Scientific advisor Cardiology Apply locations Citi Center - MX time type Full time posted on Posted 8 Days Ago job requisition id R1579671

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.

Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more:
careers.Bms.Com/working-with-us .

Bristol Myers Squibb es un empleador que brinda igualdad de oportunidades. Las personas que apliquen para cualquier vacante, y que estén calificadas para la misma recibirán consideración para el empleo sin distinción de raza, color, religión, sexo, orientación sexual, identidad de género, nacionalidad, edad, discapacidad, condición de veterano protegido, embarazo, ciudadanía, estado civil, expresión de género, información genética, afiliación política o cualquier otra característica protegida por la ley.

Position Summary / Objective

The position is required to perform five Core Roles and collaborates closely with the appropriate Medical Lead(s). This position is field-based.

Position Responsibilities

1. Collect and communicate medical insights

- The SA should profile the medical landscape within the Disease Area and continuously update this knowledge, including knowledge and expertise in products, patient treatment trends, unmet medical needs, clinical trials and scientific activities
- Ensure awareness of current Key Insight Questions (KIQs) and proactively contribute insights gained from healthcare provider interactions to the internal Medical team.
- Contribute to the development of Brand Plans and Strategies by communicating his or her medical insight and knowledge about the product or disease area, in particular with reference to patients needs and treatment trends and as derived from contacts with Thought Leaders, other health-care providers or payers
- Participate in the development of the Local Medical Plan and contribute to the overall Commercial Plan by leveraging medical insight and knowledge of recent scientific publications about the product or disease area
- Contribute to the development of and execute the Local Therapeutic Area Medical Plan, which should be aligned with the Europe medical plan and the Local Brand Plan

2. Scientific exchange with Thought Leaders

- Develop and maintain TL engagement plan
- Proactively or reactively interact with healthcare providers, as appropriate, through face-to-face meetings, webconferences, teleconferences, e-mail, etc.
- Develop and maintain contacts with Thought Leaders, in accordance with the strategy developed by the company 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 Health Care Providers
- Ensure appropriate response to unsolicited scientific questions or requests posed by Health Care Providers for approved Products/Brands (in and off label ), and for products in development, by 1/ providing accurate scientific data in compliance with Company Policies, and legal and ethical standards or by 2/ liaising appropriately with Medical Information
- Contribute to involvement of Thought Leaders, as required and as appropriate, in local and/or GDO driven studies and other scientific activities
- Identify the need for and execute local Advisory Boards (as appropriate).

3. Provide medical services to external customers

- Exhibit a high degree of familiarity with, and proficiency in, centrally developed scientific resources and presentations. Present information to HCPs, as appropriate, ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives
- Propose to the Brand Team scientifically meaningful medical programs such as Continuous Medical Educational Programs and Symposia and ensure flawless execution of such activities
- Identify potential speakers for BMS educational programs and ensure that these speakers receive all necessary product and disease state training.

- Contribute to the development of scientific publications or presentations, as appropriate

4. Medical support for internal stakeholders

Support &
Trainer
- As appropriate, contribute to the initial and ongoing medical/scientific disease area and product-specific training of internal BMS customers (Sales force, etc) - in collaboration with the training department, if any - enabling understanding and balanced communication of the scientific benefits of a Brand
- Provide training to Investigational Site staff, Site Managers and Monitors in BMS products, medical concepts and available therapies;
act as a champion for the medical benefits of a product or products, and as point of contact for GDO

Expert Contributor to Internal Customers
- The SA should provide scientific support to Internal Stakeholders, specifically to Marketing, Regulatory, Outcomes Research, Pharmacovigilance, Legal Counsel and Market Access
- Contribute to, supervise and coordinate the development of the medical / scientific sections of pricing and reimbursement files
- Provide medical insight for OR studies and advice on how to conduct trials

Promotional Material Contributor &
Reviewer
- Contribute to the development and review of promotional material (as appropriate, consistent with the Promotional Review SOP)

5. Provide clinical trial support

Clinical Trial/Survey Identification, Planning and Execution
- Lead the identification, at an early stage,of potential opportunities for country participation in clinical development programs, by early mapping of centers of excellence, treatment trends and recruitment potential in untapped therapeutic areas / with new compounds
- 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 GDO Hub management / EMLs on trial and survey feasibility and site suitability, based on knowledge of the field and through direct contacts with potential investigators
- Facilitate clinical trial activities between BMS and investigators for both BMS sponsored (interventional and non-interventional) and BMS supported Investigator sponsored trials (in accordance with the appropriate policies and SOPs).
- Provide support for Non Interventional Research (NIR) and Interventional Clinical Trials on an as needed basis

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.

Degree Requirements

- Medical doctor (cardiologist, immunologist, physician), and/or with experience in Cardiology within Pharma Industry or with a broad medical background
- Or Science graduate with substantial and relevant pharmaceutical experience in Cardiology

Experience Requirements

- Superior disease Area knowledge (cardiology or immunology), including key scientific publications
- In-depth knowledge of cardiology or immunology
- In-depth knowledge of relevant BMS products highly desirable.
- Knowledge of clinical trial design and process
- Knowledge of the National Healthcare System and the pharmaceutical industry
- Excellent English language skills, spoken and written
- Basic statistical techniques

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to [email protected]. Visit careers.Bms.Com/ eeo -accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.

W e’re creatinginnovative medicines for patients fighting serious diseases. We’re also nurturing our own diverse team with inspiring work and challenging career options. No matter the role, each one of us makes a contribution. And that makes all the difference.

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