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Medical affairs physician (md) / scientist (non-md) - therapeutic area lead cardiometabolic health

Bruxelles
CDI
Eli Lilly and Company
Médical
Publiée le 11 février
Description de l'offre

Medical Affairs Physician (MD) – Cardiometabolic HealthJoin to apply for the Medical Affairs Physician (MD) – Cardiometabolic Health role at Eli Lilly and Company

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life‐changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We're looking for people who are determined to make life better for people around the world.

Primary ResponsibilitiesBusiness / Customer Support (Pre and Post Launchh3>

Understand and anticipate the scientific information needs of all local customers (payers patients, health care providers)

Actively address customer (payer, patient and health care providers) questions in a timely fashion by leading data analyses, and new clinical or health outcomes research efforts

Contribute to the development of medical strategies to support brand commercialization activities by working closely with the global Medical Affairs and brand teams, Global Patient Outcomes/Real World Evidence and global PRA, clinical management or personnel and other cross‐functional management during the development of the local business plan

Contribute as a scientific and medical expert to activities and deliverables of the PRA organization, in particular giving clinical input and insight to develop payer partnership programs and defending the product value

Support business‐to‐business and business‐to‐government activities as medical expert

Contribute actively on an ongoing basis to the strategic planning for currently marketed brands

By offering scientific input, contribute to the development, review, and approval of promotional materials for the brand team

Support training of regional managers, and other medical representatives.

Become familiar with market archetypes and potential influence on the medical interventions for the product

Take a leadership role in defining the Patient Journey and corresponding Moments of Truth based on his/her medical knowledge. Become patient advocate, as well as a medical expert

Understand and apply knowledge of customer insights to all customer‐related activities

Scientific Data Dissemination / Exchange

Knowledge of and compliance with local laws and regulations, and global policies and procedures, compliance guidelines with respect to data dissemination and interactions with external health care professionals

Understand and actively address the unsolicited scientific information needs of external health care professionals according to guidelines above

Support the planning of symposia, advisory board meetings, and/or the facilitation of other meetings with health care professionals

Support medical information associates in preparation and review of medical letters and other medical information materials

Support training of local medical personnel

Prepare or review scientific information in response to customer questions or media requests

Support data analysis and the development of slide sets (through reviewing and/or approving) and publications (abstracts, posters, manuscripts)

Establish and maintain appropriate collaborations and relationships with external scientific experts, thought leaders, and the general medical community on a local, national, regional, and possibly international basis

Develop and maintain appropriate collaborations and relationships with relevant professional societies

Support the design of customer research as medical expert

Provide congress support (for example, availability to answer questions at exhibits, provide oral and poster presentations, staff medical booth, meet thought leaders, and participate in customer events)

Participate in data analyses, development of scientific data dissemination, and preparation of final reports and publications

Clinical Planning

Communicate and collaborate as needed to ensure life cycle plans for drugs in development address customer needs

Understand and keep updated with the pre‐clinical and clinical data relevant to the molecule

Represent the clinical needs of the country/region in the development of clinical strategies, development plans and study protocol design

Clinical Research / Trial Execution and Support

Collaborate with clinical research staff in the design, conduct and reporting of local clinical trials (for example, sample size, patient commitment, timelines, grants, and governance review interactions)

Participate in investigator identification and selection, in conjunction with clinical teams

Assist in the planning process and participate in study start‐up meetings and other activities to provide the appropriate scientific training and information to investigators and site personnel

Understand and actively address the scientific information needs of all investigators and personnel

Scientific / Technical Expertise and Continued Development

Be aware of current trends and projections for clinical practice and access in the therapeutic area(s) relevant to the product, both near term and longer term.

Critically read and evaluate the relevant medical literature; know the status and data from competitive products; and keep updated with medical and other scientific developments relevant to the product

General Responsibilities

Support the business unit management team, including medical leadership in preparation and administration of the local or business unit medical budget.

Actively set and meet individual professional development goals and contribute to the development of others by being an active source of coaching and feedback to co‐workers

Collaborate proactively and productively with all alliance, business, and vendor partners

Be an ambassador of both patients and the Lilly Brand

Desired Skills & Experience / Qualifications

You are a Medical Doctor with previous experience in Medical Affairs

Experience within endocrinology or cardiology is a plus

You are fluent in Dutch, French and English

You have strong communication skills and know how to interact with doctors and customers

You have excellent diplomatic skills

Able to work with high degree of autonomy

Be able to inspire others, be energetic and passionate

Able to think strategically and adapt to changing priorities

You are goal oriented and strive for innovative solutions

You like a challenge and want to explore new methods

You are a strong team player

Strong project management skills

Ability to lead several projects at same time (prioritization)

Job Details

Seniority level: Mid‐Senior level

Employment type: Full‐time

Job function: Health Care Provider

Industries: Pharmaceutical Manufacturing

LocationBrussels, Brussels Region, Belgium

Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.

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Accueil > Emploi > Emploi Santé > Emploi Médical > Emploi Médical à Bruxelles > Medical Affairs Physician (MD) / Scientist (non-MD) - Therapeutic Area Lead Cardiometabolic Health

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