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Alliance Diabetes & Obesity Crp

0-2 years
Not Disclosed
10 Feb. 11, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Alliance Diabetes & Obesity CRP
Location: Available in 7 locations
Category: Medical
Job Type: Full Time, Regular
Job ID: R-59040

Company Overview: Lilly is a global healthcare leader, headquartered in Indianapolis, Indiana. The company’s mission is to discover and bring life-changing medicines to those who need them, improve the understanding and management of diseases, and give back to communities through philanthropy and volunteerism. They strive to make life better for people around the world by uniting caring with discovery.

Key Responsibilities:

  1. Business/Customer Support:

    • Understand and anticipate the scientific information needs of local/regional customers, including payers, patients, and healthcare providers.
    • Address scientific queries through data analysis and research efforts.
    • Contribute to the development of medical strategies to support brand commercialization by collaborating with global teams, including Medical Affairs, Patient Outcomes/Real World Evidence, and Clinical Management.
  2. Scientific Data Dissemination/Exchange:

    • Comply with local laws, global policies, and regulations related to data dissemination and healthcare provider interactions.
    • Support the preparation of medical letters and information materials for external professionals.
    • Build relationships with external scientific experts and the medical community at local, regional, and international levels.
  3. Clinical Planning & Research Support:

    • Represent clinical needs to the business unit medical leadership in developing clinical strategies and study protocols.
    • Ensure appropriate communication of risk to study subjects by reviewing informed consent documents and risk profiles.
    • Collaborate with clinical research teams in trial design, conduct, and reporting.
  4. Regulatory Support Activities:

    • Assist in the development and review of local labeling in collaboration with global teams, regulatory, and legal.
    • Provide medical expertise to regulatory scientists and participate in advisory committees.
  5. Scientific Technical Expertise:

    • Stay updated on clinical practice trends and projections for relevant therapeutic areas.
    • Evaluate the latest medical literature and competitive product data to maintain a deep understanding of the therapeutic area.
    • Serve as a scientific consultant and protocol expert for clinical study teams.

Qualifications:

  • Medical Doctor (MD) or Doctor of Osteopathy (DO), board eligible or certified in the relevant specialty or subspecialty, or equivalent post-medical school training.
  • Fluency in English, both verbal and written.
  • Knowledge of the drug development process in the country/region is preferred.
  • Strong communication, organizational, and negotiation skills.
  • Ability to influence and create a positive working environment.

Additional Information:
Lilly is committed to ensuring equal opportunities for individuals with disabilities to engage in the workforce. If accommodations are needed for the application process, individuals are encouraged to request assistance.

Non-Discrimination Policy:
Lilly does not discriminate based on 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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