Clinical Research jobs in United States
Explore 421 matching jobs.
Director – Clinical Research Physician, Pain
Eli Lilly and Company
Posted: 10/21/2026Distinguished Scientist, Clinical Research, Thoracic Malignancies
MSD
Posted: 10/21/2026Clinical Research Associate II
BeOne Medicines
Posted: 10/21/2026Associate Director, AI Clinical Scientist
Otsuka Pharmaceutical Companies (U.S.)
Posted: 10/21/2026Senior Clinical Study Manager
Intuitive
Posted: 10/21/2026Overnight Clinical Research Nurse – PRN
ICON plc
Posted: 10/21/2026Clinical Trial Manager
Iovance Biotherapeutics, Inc.
Posted: 10/20/2026Clinical Research Project Manager – Hybrid
University of Pennsylvania Perelman School of Medicine
Posted: 10/20/2026Clinical Trial Manager, Senior – Oncology
Boehringer Ingelheim
Posted: 10/20/2026Clinical Research Project Manager – A-B
Penn Information Systems & Computing
Posted: 10/20/2026Clinical Research Associate
ICON plc
Posted: 10/20/2026Clinical Research Associate
Syneos Health
Posted: 10/20/2026Senior Clinical Research Associate
ICON plc
Posted: 10/20/2026Clinical Research Associate – Sponsor Dedicated
IQVIA
Posted: 10/20/2026Senior Clinical Research Associate – Psychiatry
Worldwide Clinical Trials
Posted: 10/20/2026Clinical Research Nurse – Home Visits
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse – Home Visits, PRN
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse – Home Visits
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse – Home Visits
WEP Clinical
Posted: 10/20/2026Clinical Research Nurse, Home Visits
WEP Clinical
Posted: 10/20/2026
Director – Clinical Research Physician, Pain
Eli Lilly and CompanyCore Competencies
Role fitUse this summary to align your resume positioning with the role.
Demonstrates expertise in medical leadership and clinical trial design, with a strong focus on analgesic studies and regulatory compliance. Possesses clinical development experience and the ability to interpret clinical trial data effectively.
About the role
Key responsibilities & impact- Provide medical and scientific leadership to the business and/or therapeutic area
- Provide scientific expertise and consultative support to product teams, internal Lilly partners, external organizations, regulatory agencies, and external partners
- Perform medical monitoring for one or more large, multicenter, multinational analgesic clinical trials
- Support phase 2 proof-of-concept and dose-finding studies
- Author regulatory documents
- Act as a scientific and medical resource for study teams, departments, and others
- Ensure activities comply with local and international regulations, laws, guidance, GCPs, company standards, Lilly policies and procedures, integrity agreements, and Principles of Medical Research
- Collaborate with diverse teams in the clinical neuroscience organization
- Support analgesic clinical trial design and early clinical development
- Interpret clinical trial efficacy and safety data
Requirements
What you’ll need- Medical Doctor or Doctor of Osteopathy
- Board-eligible or certified in anesthesiology, neurology, rheumatology, psychiatry, or physical medicine and rehabilitation, or comparable post-medical school clinical training relevant to the country of hiring
- U.S.-trained physicians must have achieved board eligibility or certification
- Non-U.S.-trained physicians must have completed education and training at a medical school meeting LCME requirements
- Minimum of 2 years of clinical development experience in an industry setting, including medical monitoring and/or regulatory submissions
- Fluent in English, written and verbal
- Experience in diagnosis and clinical management of acute and chronic pain and/or subspecialty pain medicine certification preferred
- Clinical skills and development experience in use disorder and psychiatric populations preferred
- Interest in early clinical development and analgesic clinical trial design
- Comfortable working with electronic data capture, case report forms, medical listings, Spotfire or other medical data visualization, and interpreting clinical trial efficacy and safety data
- Knowledge of the drug development process
- Expertise in one or more areas relevant to clinical trials strongly preferred, such as statistical/inferential methods, rating instruments, regulatory standards, safety assessment, or investigator/site management
- Demonstrated interpersonal, organizational, teamwork, and negotiation skills
- Ability to influence others cross-functionally and within the function
- Demonstrated success implementing projects
- Willingness to engage in limited domestic and international travel
- Publication record
- Ability to work EST standard business hours
Benefits
Comp & perks- Company bonus depending on company and individual performance
- Company-sponsored 401(k)
- Pension
- Vacation benefits
- Medical, dental, vision, and prescription drug benefits
- Flexible benefits, including healthcare and/or dependent day care flexible spending accounts
- Life insurance and death benefits
- Time off and leave of absence benefits
- Well-being benefits, including employee assistance program, fitness benefits, and employee clubs and activities
- Employee resource groups and support networks
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