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June

Associate Medical Lead

Bristol Myers Squibb - Mulgrave, VIC

Health, Medical & Pharmaceutical
Source: uWorkin

JOB DESCRIPTION

Full Job Description
At Bristol Myers Squibb, we are inspired by a single vision - transforming patients’ lives through science. In oncology, hematology, immunology and cardiovascular disease - and one of the most diverse and promising pipelines in the industry - each of our passionate colleagues contribute to innovations that drive meaningful change. We bring a human touch to every treatment we pioneer. Join us and make a difference.

Associate Medical Lead: Immuno-Oncology

Associate Medical Leads (MLs) have both an internal and external focus to their role. From an internal perspective, the Associate ML will support the Medical team by providing scientific expertise on topics that impact all tumour types including but not limited to creation of irAR materials, review of ARMA materials, management of regulatory documents (e.g. Product Information), SOP and compliance initiatives, clinical guidelines and input into all activities related to the posology of the product (e.g. dosing, formulation). Further to the scientific expertise, the role will also play a very practical role by assisting the medical team in the logistics of contracting, sponsorships and medical events.

Associate MLs are also externally-focused experts in medical science who can engage in influential conversations with key thought-leaders, multi-disciplinary team (MDT) specialists (e.g. gastroenterologists, endocrinologists) and the internal BMS organisation with the overall goal of improving patient care to help patients prevail over serious diseases. The Associate ML will be involved in gathering and understanding insights on current and future disease management and scientific perspectives including unmet clinical needs. Associate MLs will make a strong contribution as a full member of the matrix brand team. They are accountable for developing and delivering innovative medical activities such as medical education, high quality materials and leading strategy discussions.

Purpose of the job:
The BMS Australia Medical team translate and generate good science to optimise patient care and access to medicines by collaboration with external and internal stakeholders, scientific influencing and delivery of external impact for patients and their HCPs. Outcomes desired include advocacy and activities with impact on speed of access to patients, external and internal partnerships/projects that deliver better patient care and advance the science, exceptional levels of customer experience.

Key Responsibilities and Major Duties:
1. External Environment and Customer Focus

Develop and maintain strong working relationships with a group of key Thought Leaders and MDT specialists that are relevant to pan-tumour topics, gathering insights on current and future disease and safety management and scientific perspectives including unmet clinical needs. Understand insights gathered from scientific conversations to inform medical activities and clinical research locally and globally, as well as informing brand team, where appropriate.

Engage in scientific dialogue both internally and externally around current and emerging data/guidelines through field visits, presentations and participation at scientific congresses.

Actively profile the medical landscape and continuously update knowledge and expertise in irAR management, patient treatment trends, unmet medical needs, clinical trial data, clinical guidelines and scientific activities.

2. Input into the Medical Plan

Provide medical input into development of Brand strategic and tactical plans on topics that cover all tumours.

Be a proactive member of the Brand team providing medical input and contributing as a full member of the medical team.

Initiate, develop and deliver flawlessly medical activities such as medical education, medical materials and strategic discussions.

Focus on better patient outcomes through innovation and simplification of all activities.

Identify and train potential speakers for BMS educational programs (e.g. irAR management)

3. Provide Medical Support

Lead the medical contribution to the development and review of medical content that is relevant across all tumours.

Contribute to and coordinate the development of the medical / scientific sections of regulatory and PV documents.

Contribute to the development of scientific publications or presentations as required.

Support the initial and ongoing medical/scientific training and provide key scientific/clinical updates to internal stakeholders (Commercial, Regulatory, OR, PV, Legal, HEOR, Market Access, etc).

Ensure that BMS Pharmacovigilance procedural documents and BMS SOPs that are relevant to this role and the wider medical department are understood and applied by all internal and external stakeholders.

Provide logistical and procedural support to the Medical Department that relates to contracting, sponsorships and medical meetings.

4. Support Clinical Trial Activities

Support Clinical Operations and Non Regulatory Data generation studies, including input on study feasibility, identification and assessment of potential study sites, facilitate BMS and investigator activities, and conduct site visits to support patient recruitment and/or discussions as needed.

Provide recommendations and insights to GCO on study and site feasibilities within the therapeutic area based on knowledge of the field and through direct contacts with potential investigators.

Actively support CRO sponsored studies as appropriate.

Provide medical support to RCO 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.

At all times, Associate MLs will perform their activities in an ethical and compliant manner, acting with the highest integrity in adherence with all BMS policies and external laws and regulations.

(Disclaimer: The responsibilities listed above are only a summary and other responsibilities will be requirements as assigned)

Qualifications, experience and competencies:
PharmD or PhD, ideally with experience in immune-oncology or with a broad medical or scientific background Or Science graduate with substantial and relevant pharmaceutical experience

Working in a medical, scientific and/or clinical research environment

Discussing scientific or clinical data to help understand medical and scientific insights from physicians to improve patient outcomes.

Effectively listening, communicating and presenting scientific and/or clinical data to research or healthcare professionals

Developing peer-to-peer relationships with top-ranking doctors, scientists or other healthcare professionals

Training others

Quickly and comprehensively learning about new subject areas and environments

Medical scientific knowledge and understanding in a disease area

In-depth knowledge of pharmaceutical processes and the regulatory environment.

Knowledge of clinical trial design and process

Knowledge of the National Healthcare System and the pharmaceutical industry

Excellent English language skills, spoken and written

Around the world, we are passionate about making an impact on the lives of patients with serious diseases. Empowered to apply our individual talents and diverse perspectives in an inclusive culture, our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

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.

Mulgrave, VIC

Health, Medical & Pharmaceutical




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