Associate Medical Director / Principal Investigator – Clinical Research
Job ID: R-01324887
Job Type: Full-Time
Category: Clinical Research
Work Arrangement: Fully Onsite
Locations: Available in 5 U.S. locations (including Las Vegas)
Schedule: Monday–Friday (approx. 7 AM–3 PM) + light rotational weekend call
About the Role
Thermo Fisher Scientific is seeking a motivated Physician to serve as Associate Medical Director/Principal Investigator at the Las Vegas Clinical Research Unit (CRU). This physician will provide medical oversight, ensure protocol compliance, and serve as the investigator for assigned clinical trials in a busy Phase 1, 32-bed unit.
This role is critical for ensuring subject safety, regulatory adherence, and high-quality clinical research delivery.
Eligibility Requirements
Must be legally authorized to work in the U.S. (No sponsorship available)
Must pass a comprehensive background check, drug screen, and meet credentialing requirements
Requires Physician status (MD or DO)
Must obtain Nevada State medical license (if not already licensed)
Key Responsibilities
1. Protocol & Study Oversight
Review study protocols for scientific, logistical, and safety feasibility.
Follow client directives and ensure strict adherence to study protocols.
Represent investigator responsibilities as described in FDA Form 1572.
Present first-in-human and other high-risk studies to the Human Safety Committee (HSC).
Work with project managers to develop Risk Management Plans (RMPs).
2. Clinical Duties
Conduct screening exams, physicals, and ensure proper informed consent.
Manage safety issues for individual subjects and full cohorts.
Respond to medical emergencies and make protocol-guided safety decisions.
Monitor adverse events, ECG/lab abnormalities, and medical status changes.
Assess causality and clinical significance of abnormal findings.
3. Regulatory & Quality Compliance
Ensure all trial activities follow:
ICH-GCP guidelines
FDA regulations
Local, national, and organizational policies
Review and sign:
Medical data
Case Report Forms (CRFs)
Clinical Study Reports (CSRs)
4. Cross-Functional Collaboration
Consult with clients regarding protocol interpretation and safety decisions.
Provide study-related medical training to internal teams.
Maintain strong and transparent communication with clients, investigators, and the clinical team.
Support operational and business development staff as needed.
5. Additional Responsibilities
Support quality initiatives and regulatory compliance within the CRU.
Participate in process improvement activities.
Provide weekend on-call coverage (rotational, approx. every 3–4 weekends).
Required Qualifications
Education & Licensing
MD or DO degree
Unrestricted medical license (Nevada license required upon employment)
Board certification (preferred)
Valid ICH-GCP certification (can be completed post-hire)
Experience
No prior clinical research experience required (experience preferred).
Must have strong general medical diagnostic and treatment capability.
Required Skills
Understanding of regulatory requirements (FDA, ICH-GCP)
Ability to evaluate safety and tolerability of investigational drugs
Familiarity with drug development and clinical trial lifecycle
Strong judgment, discretion, and problem-solving abilities
Excellent decision-making, negotiation, and influencing skills
High accuracy and attention to detail
Excellent written and verbal communication
Ability to work independently and in collaborative environments
Proficiency with common computer applications
Work Environment
Office-based work with exposure to standard office equipment
Monday–Friday | 7 AM–3 PM (approx.)
Light weekend call rotation (every 3rd or 4th weekend)
Compensation
Estimated Salary Range (Nevada):
$200,000 – $278,900 annually
Plus:
Annual performance-based bonus eligibility
Benefits – U.S. Total Rewards Package
Health & Wellness
National medical, dental, and vision plans
Health incentive programs
Employee Assistance Program (EAP)
Family support programs
Leave & Time Off
120+ hours PTO annually
10 paid holidays
Paid parental leave:
3 weeks bonding
8 weeks caregiver leave
Financial & Career Benefits
401(k) with competitive company match
Employee Stock Purchase Plan (ESPP)
Tuition reimbursement
Commuter benefits
Insurance
Life insurance
Short-term & long-term disability
Accident insurance
Company Culture
Thermo Fisher promotes a culture based on integrity, intensity, involvement, and innovation, offering strong career growth opportunities in an impactful, mission-driven environment.
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