Principal Investigator
Pharmaron
Summary
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. Clinical research experience is welcomed but not required. 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.
Job description
Key Responsibilities
Clinical Leadership
- Serve as Principal Investigator or Sub-Investigator for Phase I-III 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
Study Execution & Scientific Collaboration
- 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
Regulatory & Quality Oversight
- 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
Team Leadership
- 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
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
Benefits
- Medical, Dental & Vision
- 401(k) Matching
- Paid Time Off
- Paid Sick Leave
- Company Holidays
- Health Savings Account
- Flexible Spending Accounts
- Life Insurance
- AD&D Insurance
- Short-term Disability
- Long-term Disability
- Employee Assistance Program
- Fertility Support
- Maternity Resources
- Professional Development
Company overview
Pharmaron is a premier global life sciences service provider founded in 2004, offering comprehensive research, development, and manufacturing services throughout the entire drug discovery and development process. As a leading Contract Research Organization (CRO) and Contract Development and Manufacturing Organization (CDMO), Pharmaron provides integrated solutions across multiple therapeutic modalities including small molecules, biologics, and cell and gene therapy (CGT) products. The company's extensive service portfolio encompasses synthetic and medicinal chemistry, biology services, DMPK (drug metabolism and pharmacokinetics), pharmacology, toxicology, radiochemistry, CMC (chemistry, manufacturing, and controls), and clinical development services. With over 10,000 employees worldwide and facilities across China, the United States, and Europe, Pharmaron supports pharmaceutical and biotechnology companies in accelerating their R&D programs from early discovery through commercial manufacturing. The company is publicly listed on both the Shenzhen and Hong Kong stock exchanges and maintains a strong commitment to scientific excellence, regulatory compliance, and technological innovation in the life sciences sector.