Principal Investigator

Pharmaron • Baltimore, MD

17h • $200,000 - $285,000 • Onsite

About The Position

Pharmaron is seeking an experienced physician to serve as a Principal Investigator within our growing Phase I Clinical Research Unit in Baltimore, Maryland. This is a unique opportunity for a board-certified physician who is passionate about advancing medicine through clinical research while maintaining a strong focus on participant safety and quality care. Physicians with backgrounds in Internal Medicine, Family Medicine, Emergency Medicine, or related specialties are encouraged to apply. As Principal Investigator, you will provide medical leadership for early-phase clinical studies, oversee participant safety, collaborate with sponsors and scientific teams, and help shape the future growth of our clinical research programs.

Requirements

• MD or DO degree from an accredited medical school
• Board Certification in a recognized specialty
• Active and unrestricted medical license
• Minimum 5 years of clinical practice experience
• Current CPR and ACLS certifications
• Strong understanding of patient care, medical ethics, and clinical decision-making
• Excellent communication and leadership skills

Nice To Haves

• Previous clinical research experience as a Principal Investigator, Sub-Investigator, or treating physician
• Experience supporting Phase I or early clinical development programs
• Familiarity with ICH-GCP, FDA regulations, and clinical trial operations
• DEA registration
• Background in Internal Medicine, Family Medicine, or Emergency Medicine

Responsibilities

• Serve as Principal Investigator or Sub-Investigator for Phase I clinical studies
• Provide medical oversight and ensure participant safety throughout study conduct
• Review eligibility, medical histories, adverse events, and safety data
• Conduct physical examinations and medical assessments as required
• Partner with sponsors and internal teams on protocol review, study design, and implementation
• Support dosing activities and ongoing medical monitoring
• Contribute to study interpretation, reporting, and regulatory submissions
• Provide scientific and medical consultation to project teams and clients
• Ensure studies are conducted in compliance with ICH-GCP, FDA regulations, and applicable guidelines
• Maintain protocol integrity and oversight responsibilities as listed on FDA Form 1572
• Support inspections, audits, and regulatory interactions when required
• Mentor and guide Clinical Research Coordinators, nurses, and study staff
• Promote a culture of participant safety, quality, and operational excellence
• Collaborate closely with Medical, Clinical Operations, Pharmacy, Laboratory, and Business Development teams

Benefits

• Insurance including Medical, Dental & Vision with significant employer contributions
• Employer-funded Health Reimbursement Account
• Healthcare & Dependent Care Flexible Spending Accounts
• 100% Employer-paid Employee Life and AD&D Insurance, Short- and Long-Term Disability Insurance
• 401k plan with generous employer match
• Access to an Employee Assistance Program

What This Job Offers

• Job Type: Full-time
• Career Level: Principal
• Education Level: Ph.D. or professional degree