Clinical Research Physician (Psychiatry or General Medicine) – Part-Time
Job ID: R-01335575
Employment Type: Part-Time
Work Mode: Fully Onsite
Location: Atlanta, Georgia, United States
Category: Clinical Research | Medical Affairs | Physician Roles
Experience Required: Minimum 1+ year
Work Schedule: Standard (Monday to Friday, Part-Time)
About the Organization
Our Clinical Research Services team plays a critical role in accelerating the development of innovative therapies that address some of the world’s most complex health challenges. As part of a leading global Contract Research Organization (CRO), the team supports the PPD® clinical research portfolio and delivers high-quality clinical trial execution across more than 100 countries.
Thermo Fisher Scientific is driven by a global mission to enable customers to make the world healthier, cleaner, and safer by advancing clinical research, development, and delivery of life-changing treatments.
Role Overview
The Clinical Research Physician (Psychiatry or General Medicine) will support onsite clinical trials at a dedicated research site in Atlanta, Georgia. This part-time role is ideal for physicians seeking hands-on involvement in clinical research while maintaining flexibility in work schedules.
The physician will be responsible for ensuring participant safety, clinical oversight, protocol compliance, and high-quality execution of clinical studies in accordance with ICH-GCP, regulatory requirements, and site procedures.
Part-Time Schedule Details
Psychiatry: Approximately 3 days per week, ~5 hours per day
General Medicine: Approximately 4 days per week, ~3 hours per day
Some flexibility in scheduling may be accommodated based on site needs
Key Responsibilities
Clinical Oversight & Patient Safety
Conduct clinical evaluations and medical assessments to determine participant eligibility
Ensure participant safety, wellbeing, and ethical conduct throughout the study lifecycle
Provide continuous medical oversight for active clinical trials
Study Execution & Quality
Execute clinical trials in compliance with ICH-GCP, study protocols, SOPs, and local regulations
Review enrollment progress, screening success rates, screen failures, and participant retention
Interpret study protocols and Investigator’s Brochures (IBs)
Support patient recruitment strategies in collaboration with site teams
Documentation & Compliance
Maintain accurate source documentation and clinical records
Report safety events, protocol deviations, quality issues, and complaints per site procedures
Support audit readiness, inspections, and regulatory reviews
Oversee investigational medicinal product (IMP) management as applicable
Education, Experience & Licensure
Required Qualifications
Medical Doctor (MD or equivalent) with valid registration in the country of practice
Active, unrestricted medical license in good standing
Minimum 1+ year of experience in clinical research, or comparable clinical/research experience demonstrating capability to work in clinical trials
Valid ICH-GCP certification (may be obtained post-hire)
Legal authorization to work in the United States without sponsorship
Ability to pass background check and drug screening
Preferred Qualifications
Formal training or specialization in Psychiatry (strongly preferred for psychiatry studies)
Experience in clinical trial environments, site-based research, or regulated healthcare settings
Knowledge, Skills & Competencies
Strong understanding of medical terminology, drug safety, and laboratory data interpretation
High attention to detail with strong documentation and administrative skills
Proficiency in Microsoft Office and sponsor-related clinical systems and portals
Ability to work independently while collaborating effectively with multidisciplinary teams
Strong time management, prioritization, and multitasking skills
Ability to perform under pressure and meet study timelines
Sound understanding of ethical, commercial, and operational considerations in clinical research
Work Environment & Physical Requirements
Office-based clinical research environment
Ability to remain stationary for 4–8 hours per day
Frequent interaction with study participants and site personnel
Light to moderate lifting (up to 15–20 lbs), including clinical materials and equipment
Frequent use of computers and electronic clinical systems
Regular attendance required
Why This Opportunity?
This role offers physicians the opportunity to contribute directly to high-impact clinical research while maintaining part-time flexibility. You will be part of a globally respected research organization, working at the forefront of patient-focused clinical development and advancing innovative therapies that improve lives worldwide.
Thermo Fisher Scientific fosters a culture of integrity, collaboration, innovation, and professional growth, providing meaningful career development opportunities within clinical research.
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Ranchi |Sikkim :
Rangpo |India :
Siliguri |Illinois :
Abbott Park | Bloomingdale | Champaign | Chicago | Deerfield | Glenview | Lake Forest | Lombard | Naperville | Norridge | Park RIdge | Round Lake |Maryland :
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
Arizona | Buffalo Grove | Clayton | Downers Grove | fairmont | Georgia | Keene | Michigan | Mt. Pleasant | New Jersy | OH | Piedmont | Salisbury | United States | Whitesboro | Winston-Salem |Georgia :
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Frank Scottile Blvd |Missouri :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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China | Quarry Bay |Liaoning :
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Netherlands |Remote Australia :
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England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
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Tallinn |Hà Nội :
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Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
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