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.

You will be the first member of the cross-functional team that will be put in place to support the (pre-)launch of a new molecule in Alzheimer’s disease.

We are ideally looking for a physician with medical affairs experience with strong strategic, cross-functional teamwork and leadership skills. You will be in charge of the development and the execution of the medical plan in line with product/disease state strategy, project/budget management, thought leader engagement, identifying data gaps for getting product access and training of sales force. On top of the medical projects, the Clinical Research Physician/Clinical Research Scientist has a broad responsibility, requiring teamwork with the reimbursement department, the RWE manager, the marketing and clinical operations department.

You are a member of the Medical Affairs Team and are reporting to the Medical Director in Belgium.

RESPONSIBILITIES

Business/customer support (pre and post launch support)

In depth product knowledge and knowledge of the therapeutic area (Alzheimer’s disease) and the treatment optionsContribute 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 Price, Reimbursement and Access (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 defend the product value.By offering scientific and creative input, contribute to the development, review, and approval of promotional materials for the brand team.Support training of sales representatives, 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 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 (if they cannot be answered by medical information service)Organize advisory board meetings and/or other meetings with health care professionals.Support medical information associates in preparation and review of medical letters and other medical information materials.Support development of slide sets and publications (abstracts, posters, manuscripts).Establish and maintain appropriate collaborations and relationships with external scientific experts, thought leaders.Develop and maintain appropriate collaborations and relationships with relevant professional societies.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).

Clinical Research

Understand and keep updated with the pre-clinical and clinical data relevant to the molecule.Identify data gaps and generate RWE to support local access.Participate in investigator identification and selection, in conjunction with clinical teams.Review IIT proposals and publications, and guide in submission of the proposal.

Regulatory Support Activities

Participate in review of local labeling collaboration with Regulatory Affairs.Demonstrate deep knowledge of local label.

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 (1-2 years) and longer-term (3-5 years).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.Responsible for the scientific training of the clinical study team.Act as scientific consultant for clinical study team members, others in medical and cross-functionally.Attend, contribute and participate in medical congresses/scientific symposia.

General Responsibilities

Follow up of the 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 in the spirit of development, increased team effectiveness and cohesiveness.Collaborate proactively and productively with all alliance, business, and vendor partners.Model the leadership behaviors.Be an ambassador of both patients and the Lilly Brand.

PROFILE REQUIREMENTS

Preferably Medical DegreeMedical affairs experienceExpertise and network in Alzheimer would be an advantageFluent in English, French and DutchExpertise in literature identification and evaluationAbility to ‘translate’ scientific data into meaningful and clear content for customer communications and engagementAbility to effectively partner cross-functionally including Marketing and Sales, PRA, RWE with strong leadership skillsStrong interpersonal and communication skillsExperience in project managementYou have a proactive approachAbility to work effectively and share information within a teamManage high workload including ability to manage and prioritize broad deliverables of a complex natureGood presentation skillsDemonstrated ability to balance scientific priorities with business prioritiesProficiency in computer skills

Why would you join TEAM Lilly?

If you like to:

Have a broad responsibilityWork in an exciting culture, based on respect for people, striving for excellence and high integrityWork in a cross-functional environment based on collaboration and team spiritBe part of a continuous innovating companyInvest in your personal developmentHave a high level of autonomy in your daily activitiesHave a flexible working environment (e.g. homeworking, …)Profit from a competitive salary & benefit package

Then you should definitely join us!

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