Principal Investigator

Pharmaron Beijing Co. Ltd.; Baltimore (MD); On-site; USD 200,000 - 285,000; Full time

Benefits offered by this job

Medical, Dental & Vision Insurance

401(k) Retirement Plan

Paid Time Off

Health Savings Account contributions

Life Insurance

Employee Assistance Program

Fertility resources

Professional development

Job summary

Pharmaron is seeking a Principal Investigator to lead early-phase clinical trials in Baltimore, MD, onsite. This role provides medical leadership, participant safety oversight, and collaboration with sponsors and internal teams to drive study success.

Ideal candidates hold an MD/DO with board certification and an active license, plus 5+ years of clinical practice. Experience in Phase I/early development and FDA/ICH-GCP familiarity are preferred.

Qualifications

• 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

Responsibilities

• 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
• 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

Skills

MD/DO

Board Certified

Medical license

Clinical experience

CPR/ACLS

Communication

Leadership

Education

MD/DO degree

Job description

Position: Principal Investigator

Salary Range: $200 - $285k (DOE)

Location: Baltimore, MD (On-site)

About Pharmaron

Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.

We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit www.pharmaron.com.

What You'll Do

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.

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

What We're Looking For:

Required Qualifications

• 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

Preferred Qualifications

• 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

Why Pharmaron?

Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.

Collaborative Culture:

You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.

Benefits:

• Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
• 401(k) Retirement Plan with generous employer matching
• Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
• Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
• 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
• Employee Assistance Program (EAP), mental health resources, and wellness programs
• Family-friendly benefits, including fertility support and maternity resources
• Professional development and career growth opportunities within a leading global CRO/CDMO

As an Equal Employment Opportunity and