Clinical Research Physician – Pain

2+ years

Not Disclosed

Remote, USA

10 Jan. 31, 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 – Pain
Location: Remote (U.S. East Coast hours)
Category: Research & Development
Job Type: Full-Time, Regular
Job Id: R-76026

Company Overview:

At Eli Lilly, we unite caring with discovery to make life better for people around the world. With more than 140 years of innovation, we strive to bring life-changing medicines to those in need, improve disease management, and give back to communities through philanthropy and volunteerism. Headquartered in Indianapolis, Indiana, we are a global leader in healthcare, with a dedicated team committed to making a meaningful impact on global health.

Position Overview:

As a Clinical Research Physician (CRP) – Pain, you will provide medical and scientific leadership in the field of analgesics and pain management. You will work on large, multinational clinical trials, phase 2 proof-of-concept and dose-finding studies, while also ensuring the integrity and compliance of clinical research processes. This role requires deep expertise in the diagnosis and clinical management of pain, including acute and chronic conditions, as well as experience in regulatory submissions and medical monitoring.

Key Responsibilities:

Lead the medical monitoring and scientific oversight of large, multicenter, multinational clinical trials focused on pain management.
Provide consultative medical expertise to product teams, regulatory agencies, and external partners.
Ensure all activities comply with local and international regulations (FDA, ICH, CPMP) and adhere to Good Clinical Practices (GCP) and Lilly policies.
Author regulatory documents and medical study reports.
Collaborate with cross-functional teams, including R&D, regulatory affairs, and safety teams, to design and execute early clinical trials for analgesic treatments.
Offer scientific guidance on clinical trial design, data analysis, and interpretation, particularly in pain management.
Ensure continuous improvement of clinical trial efficiency by identifying and implementing best practices.
Engage in medical research activities that contribute to advancing scientific knowledge in pain management.
Travel domestically and internationally as needed to support clinical trials and project teams.

Basic Qualifications:

Medical Doctor (MD) or Doctor of Osteopathy (DO).
Board eligibility or certification in anesthesiology, neurology, rheumatology, psychiatry, physical medicine and rehabilitation, or a related field.
A minimum of 2 years of clinical development experience in an industry setting, including medical monitoring and/or regulatory submissions.
Fluent in both written and verbal English communication.

Preferred Qualifications:

Experience in the diagnosis and clinical management of acute and chronic pain.
Subspecialty certification in pain medicine is highly preferred.
Experience with clinical trial design and regulatory standards for analgesics.
Familiarity with electronic data capture systems, case report forms, and medical data visualization tools such as Spotfire.
Strong communication and interpersonal skills, with the ability to collaborate effectively across teams.
Publication record in relevant medical or clinical research journals.
Knowledge of the drug development process, including safety assessments and investigator/site management.

Additional Skills:

Strong organizational and teamwork skills with the ability to influence others in a matrix environment.
Ability to effectively lead and manage projects with cross-functional teams.
Demonstrated success in clinical trial design and execution.
Comfort with a flexible work environment and ability to work remotely while maintaining EST business hours.

Additional Information:

Location: This position offers flexibility but candidates must be able to work U.S. East Coast (EST) standard business hours.
Lilly offers a comprehensive benefits program, including health and wellness programs, paid time off, retirement plans, and opportunities for professional development.

Equal Opportunity Employer:

Eli Lilly is an equal opportunity employer and does not discriminate based on age, race, color, religion, gender, sexual orientation, gender identity, national origin, disability, or any other legally protected status.

#WeAreLilly

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Clinical Research Physician – Pain

Job Description

Company Overview:

Position Overview:

Key Responsibilities:

Basic Qualifications:

Preferred Qualifications:

Additional Skills:

Additional Information:

Equal Opportunity Employer:

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