Clinical Research Physician - Us & Global Medical Affairs

2+ years

Not Disclosed

Indianapolis

10 Jan. 28, 2025

Job Description

Job Type: Full Time Education: B.Sc, M.Sc, B.Pharm, M.Pharm, LifeScience Graduates 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: Clinical Research Physician - US & Global Medical Affairs, Substance Use Disorders
Location: Indianapolis, Indiana, United States
Job Type: Full-Time, Regular
Job ID: R-76893

About Lilly:

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, with a team dedicated to improving the lives of those in need through innovative medicines. We work to enhance disease management, advance the science of healthcare, and give back to our communities through volunteerism and philanthropy. We are looking for individuals who are passionate about making a global impact and improving lives through their work.

Position Overview:

We are seeking a Clinical Research Physician (CRP) to join our Neuroscience Business Unit. This position will focus on Substance Use Disorders and is essential in supporting the company's medical strategy to meet the needs of patients, healthcare providers (HCPs), and payers. The CRP will collaborate with global teams to manage the entire lifecycle of drug development, from clinical trial design and execution to scientific communication and market support. This role is key to supporting both the development and commercialization phases, especially for late-phase and marketed products.

Responsibilities:

1. Business/Customer Support (Pre and Post Launch)

Understand and address the scientific needs of customers, including payers, patients, and healthcare providers.
Lead scientific efforts to address clinical questions and contribute to the development of medical strategies in collaboration with global teams.
Provide medical guidance on pricing, reimbursement, and access (PRA) plans, and support interactions with regulatory and government agencies.
Contribute to the development and approval of promotional materials for the brand team.
Support training of sales representatives and other medical personnel, ensuring alignment with the brand's strategic goals.
Help define the Patient Journey and Moments of Truth, advocating for the patient experience.

2. Scientific Data Dissemination/Exchange

Comply with local laws, regulations, and global policies for scientific data dissemination.
Address unsolicited scientific queries from healthcare professionals and provide up-to-date medical information.
Support the preparation of scientific materials (e.g., abstracts, posters, manuscripts) for medical congresses.
Maintain relationships with external scientific experts, thought leaders, and the broader medical community.
Participate in scientific symposia, advisory boards, and other healthcare professional meetings.

3. Clinical Planning and Execution

Collaborate with global and local teams to ensure clinical trials meet regional needs.
Contribute to the design and execution of Phase 3b/4 studies and other clinical programs.
Review and approve informed consent documents, ensure compliance with Good Clinical Practices (GCP), and address patient safety concerns during clinical trials.

4. Regulatory Support Activities

Provide medical expertise during regulatory interactions, including the development of local product labels and responses to regulatory queries.
Participate in the preparation of regulatory reports and submissions, ensuring alignment with local and global strategies.
Support risk management activities in collaboration with global teams.

5. Scientific/Technical Expertise and Professional Development

Stay updated on the latest trends in clinical practice, scientific literature, and relevant drug development processes.
Contribute to the scientific training of clinical teams and provide expertise during protocol development.
Participate in medical congresses, scientific symposia, and other professional development activities.

6. General Responsibilities

Collaborate with cross-functional teams to ensure alignment with the business unit’s goals.
Contribute to the development of the team by providing coaching and feedback to colleagues.
Participate in recruitment, diversity, and retention efforts as applicable.
Model leadership behaviors and act as a trusted ambassador of both Lilly and its patients.

Qualifications:

Minimum Requirements:

Medical Doctor (MD) or Doctor of Osteopathy (DO), board-eligible or board-certified in an appropriate specialty/subspecialty.
Completion of medical education at a school accredited by the Liaison Committee on Medical Education (LCME).

Additional Preferences:

2+ years of experience in clinical research, medical affairs, or a related field.
Strong background in Substance Use Disorders, with at least 5 peer-reviewed articles in addiction medicine/psychiatry published in the past decade.
Knowledge of the drug development process, especially in psychiatry or substance use treatment.
Proven ability to balance scientific priorities with business objectives.
Strong communication, interpersonal, teamwork, organizational, and negotiation skills.
Ability to engage in domestic and international travel to support business needs.
Fluency in English, both verbal and written communication.
Previous experience in launching medicines at Lilly or similar organizations is a plus.

Salary:

The anticipated salary for this position is between $252,000 and $369,600, depending on education, experience, and geographic location.

Benefits:

Lilly offers a comprehensive benefits package, including eligibility for a company bonus, participation in a 401(k), health insurance (medical, dental, vision), flexible spending accounts, life insurance, paid time off, and wellness programs.

Equal Opportunity Employer:

Lilly is an Equal Employment Opportunity and Affirmative Action employer. We do 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.

This position offers an exciting opportunity for a qualified individual to contribute to the field of Substance Use Disorders, directly impacting the lives of patients and healthcare professionals globally. If you're passionate about medical science and eager to make a real difference, we encourage you to apply.

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