Scientific Advisor Cardiovascular

hace 3 semanas

Buenos Aires, Argentina Bristol Myers Squibb A tiempo completo

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.

Position Summary objectives


The Scientific Advisor role is a blend of field-based and office-based time; the proportion of time the scientific advisor fulfils their internal and external duties will spend a minimum of 50 percent of their time in the field with external customers.

SAs will perform their activities in an ethical and compliant manner, in adherence with local policies and external laws and regulations.


Position Responsibilities

  • External Environment and Customer Focus
  • Develop and maintain strong relationships with Thought Leaders, appropriate HCPs, and access stakeholders, within a given geography to answer scientific, unsolicited product related questions. SAs will use various channels for interactions.
  • Effectively present reactive information to HCPs, as appropriate, ensuring medical accuracy and compliance with local procedures, ethical and legal guidelines and directives.
  • Actively profile the medical landscape and continuously update knowledge and expertise in products, patient treatment trends, unmet medical needs, clinical trials and scientific activities. Understand the competitive landscape and actively prepare to address scientific informational needs of customers.
  • Collect and provide meaningful medical insights back to the medical and commercial organizations to be actioned in support of the strategy development.
  • Implement high quality medical scientific educational programs and train internally and externally on disease state and current treatment landscape.
  • Manage and Deliver the Medical Plan
  • Participate and contribute to crossfunctional brand teams to provide strategic input into the development of Brand plans, develop and execute local Medical Plan and TL Interaction plans.
  • Deliver scientifically meaningful medical program proposals and ensure flawless execution of medical activities
  • Identify potential speakers for BMS educational programs and ensure that these speakers receive all necessary product and disease state training. Be able to train internally and externally.
  • Provide Medical Support
  • Contribute to the development and review of medical content within promotional and nonpromotional materials (as appropriate, consistent with the Promotional and Non-Promotional BMS procedural documents and/or local codes), according to local resource and requirement.
  • Contribute to the development of scientific publications or presentations, as appropriate.
  • As necessary and appropriate, may support the initial and ongoing medical/scientific area and product specific training and provide key scientific updates to internal stakeholders (Commercial, Regulatory, OR, PV, Legal, HEOR, Market Access, etc).
  • Support Clinical Trial Activities
  • Support Interventional and Non-Interventional Research (NIR) studies (including input on study feasibility, identification and assessment of potential study sites, facilitate BMS and investigator activities, and conduct site visits if requested) to support effective use of BMS investigational products, as appropriate and in agreement with local medical management.
  • Actively support CRO sponsored studies as appropriate or as defined by the study scope document
  • Provide medical support to GDO to transition patients from clinical trial to marketed and/or reimbursed supply of drug, where required and appropriate.
  • Ensure that BMS Pharmacovigilance procedural documents are understood and applied by Investigators of local studies, and alert appropriate BMS personnel to any identified Adverse Events.

Degree requirements

  • Medical degree.
  • Cardiologist.
  • Experience as attending physician as cardiologist, preferably with experience in the pharmaceutical industry. Responsibilities of the role could extend to other therapeutic areas as necessary.
  • Translate scientific or clinical data into compelling messages to help physicians best serve their patients
  • Excellent communication and interpersonal skills to interact internally in crossfunctional teams and to develop peertopeer relationships with topranking medics, scientists, or other healthcare professionals
  • Excellent English language skills, spoken and written

Uniquely Interesting Work, Life-changing Careers

On-site Protocol
Physical presence at the BMS worksite or physical presence in the field is a necessary job function of this role, which

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