Associate Medical Director/Principal Investigator - Clinical Research Opportunity!

1-3 years

$200,000 – $278,900 annually

Las Vegas Nevada

10 Nov. 28, 2025

Job Description

Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Medical Director / Principal Investigator – Clinical Research

Full-Time | Onsite | Las Vegas, Nevada
Job ID: R-01324887
Category: Clinical Research

About the Opportunity

Thermo Fisher Scientific is a global leader in scientific innovation and clinical research solutions. Through our PPD® clinical research portfolio, we support the development of life-changing therapies that address critical global health challenges. Our high-performing clinical research teams bring scientific, operational, and medical expertise to every phase of drug development.

We are seeking an Associate Medical Director / Principal Investigator to join our Clinical Research Unit (CRU) in Las Vegas, Nevada. This onsite, physician-focused role is ideal for a medically driven professional who wants to advance early-phase clinical research within a dynamic Phase I environment.

Candidates must be legally authorized to work in the United States without sponsorship and must successfully pass a comprehensive background check, including drug screening.

Role Summary

The Associate Medical Director serves as the Principal Investigator for assigned studies, ensuring all clinical trials are conducted in compliance with regulatory requirements, ICH-GCP guidelines, and organizational policies. This role provides medical leadership, oversees protocol execution, evaluates study safety, consults with clients, and supports clinical operations within a 32-bed Phase I facility.

Key Responsibilities

Provide medical oversight for assigned clinical trials as per FDA Form 1572 requirements.
Conduct informed consent discussions, screening exams, and ensure participant safety throughout the study lifecycle.
Review and assess study protocols for medical, safety, and operational feasibility.
Present high-risk or first-in-human studies to the Human Safety Committee and develop risk management plans.
Evaluate medical data, including adverse events, laboratory results, ECGs, and clinical assessments.
Oversee completion and medical sign-off for case report forms (CRFs) and clinical study reports (CSRs).
Provide medical guidance to investigators, study teams, and clients regarding inclusion/exclusion criteria and clinical decision-making.
Support quality initiatives, regulatory compliance, and process improvement activities.
Collaborate with business development staff and foster strong client relationships.
Participate in rotational weekend on-call coverage as part of the investigator team.

Required Qualifications & Experience

Education

Medical Degree (M.D. or D.O.) required.
Valid medical license in good standing; Nevada State licensure required or must be obtained.
Board Certification preferred.
Valid ICH-GCP certification (can be completed upon hire).

Experience

Clinical research experience preferred, though not mandatory.
Proficiency in general medical diagnosis, treatment, and clinical decision-making.

Skills & Competencies

Strong understanding of regulatory requirements and international clinical research guidelines.
Ability to evaluate safety profiles of investigational products and interpret complex medical data.
Excellent judgment, analytical thinking, and risk assessment capabilities.
Strong communication skills, with the ability to present complex information clearly.
High-level organization, attention to detail, and leadership capability.
Ability to work independently and collaboratively within multidisciplinary teams.
Proficiency in standard computer applications.

Working Conditions

Onsite, office-based position within a clinical research environment.
Standard schedule: Monday–Friday, approximately 7 AM – 3 PM.
Light rotational weekend coverage (every 3rd or 4th weekend).
Exposure to standard office equipment and clinical research facility operations.

Compensation & Benefits

Estimated Salary Range (Nevada): $200,000 – $278,900 annually
This role may also be eligible for variable annual bonus incentives based on individual, team, and organizational performance.

Thermo Fisher Scientific offers an industry-leading Total Rewards package, including:

Comprehensive medical, dental, and vision plans
Employee assistance programs and family support resources
Tuition reimbursement and commuter benefits
Minimum 120 hours of paid time off annually, plus 10 paid holidays
Paid parental leave for bonding and caregiver needs
Life insurance, disability coverage, and accident insurance
Competitive 401(k) retirement savings plan
Employee Stock Purchase Plan (ESPP) with discounted company stock options

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Associate Medical Director/Principal Investigator - Clinical Research Opportunity!

Job Description

Associate Medical Director / Principal Investigator – Clinical Research

About the Opportunity

Role Summary

Key Responsibilities

Required Qualifications & Experience

Education

Experience

Skills & Competencies

Working Conditions

Compensation & Benefits

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