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.
Requirements
- Participate in the research activities of the new drugs in the therapeutic area including Phase 1-3 clinical trials and RWE studies.
- Establish and maintain an appropriate collaboration with scientific experts and the medical community in general, being the medical reference providing complete, quality and transparent information on drugs in the therapeutic area.
- Support other departments/ areas of the company providing scientific information, knowledge of the pathology, clinical aspects and pharmacological management of the therapeutic area.
- Collaborate with pharmacovigilance in the correct communication of adverse effects of the drugs in the therapeutic area to the health authorities.
- Keep up to date with latest clinical guidelines, publications, current trends on clinical practice y scientific development of the therapeutic area
- Contribute to the development of the medical plan by working closely with the global medical team in the planning, initiation and follow-up of clinical trials, RWE studies and other activities included in the clinical plan.
Benefits
- Generous Paid Time Off
- 401k Matching
- Retirement Plan
- Visa Sponsorship
- Four Day Work Week
- Generous Parental Leave
- Tuition Reimbursement
- Relocation Assistance