🧪 Job Title: Clinical Research Medical Director (1-Year Fixed Term)
📍 Location: Remote – India
📅 Posted: September 2025
🕒 Job Type: Full-Time | Fixed Term (1 year)
📁 Department: Clinical Research
🏢 Employer: Thermo Fisher Scientific (PPD® – Global CRO)
🌐 Remote Status: Fully Remote
🧩 Role Overview
As a Clinical Research Medical Director (CRMA) within the PPD Functional Service Partnership (FSP) team, you will provide clinical and scientific leadership to clinical trial programs, supporting designated therapeutic areas such as:
Cardio-Renal-Metabolic
Immunology
Neuroscience
You will act as a bridge between Study Site Operations (SSO) and Medical Affairs, helping ensure trials are implemented efficiently, ethically, and with scientific integrity.
📌 Key Responsibilities
Strategic & Scientific Oversight
Serve as the country clinical development representative, offering strategic and tactical guidance on study protocols and feasibility.
Validate study designs and assess feasibility based on clinical practice, medical insight, and competitive environment.
Provide clinical input into trial planning documents, such as:
Clinical trial protocols
Informed Consent Forms (ICFs)
Concept sheets
Trial Optimization & Site Engagement
Lead clinical efforts to ensure timely trial start-up, efficient site activation, and investigator engagement.
Identify recruitment barriers and design mitigation strategies.
Facilitate collaboration between study teams, site staff, and investigators to support recruitment and retention.
Cross-Functional Collaboration
Partner with key stakeholders, including:
Clinical Trial Teams
Regulatory Affairs
Medical Information
Medical Affairs
Health Economics & Outcomes Research (HEOR)
Patient Access and Marketing
Act as a liaison with regulatory authorities, ethics committees, medical experts, and patient advocacy groups.
Safety & Quality
Ensure adherence to ICH/GCP guidelines, local regulations, and safety standards.
Provide medical support for safety-related issues in assigned studies and programs.
Monitor clinical data quality and integrity across the country/cluster.
🎓 Qualifications
Essential Requirements
Advanced degree in a scientific discipline:
MD preferred
PhD or PharmD also considered
Minimum 5+ years of experience in:
Medical Affairs
Clinical Development or Operations
PI coordination or sponsor-side clinical programs
Deep understanding of:
Clinical research processes
Drug development lifecycle
ICH-GCP principles
Fluent English communication skills – verbal and written
Ability to rapidly adapt across therapeutic areas and deliver high-quality presentations
🗓 Work Environment
Work Schedule: Standard (Monday–Friday)
Work Environment: Remote, office-equivalent setup
🌍 About Thermo Fisher Scientific
Thermo Fisher Scientific is a global leader in science, with over $40 billion in annual revenue. Through its brands (including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon, and PPD), the company delivers world-class technologies, services, and support to improve health and advance diagnostics and therapy development.
To learn more, visit: www.thermofisher.com
🌈 Equal Opportunity Employer
Thermo Fisher Scientific is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to:
Race, religion, or ethnicity
Gender identity or expression
National origin or citizenship
Disability, veteran status, or any other protected status
We are committed to fostering a culture of diversity, equity, and inclusion.
♿ Accessibility
We are committed to providing reasonable accommodations to individuals with disabilities throughout the hiring process and during employment. For assistance, please contact us to request accommodations.
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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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Mitte |Mecklenburg Vorpommern :
Rostock |Saarland :
Saarbrucken |Switzerland :
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Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Istanbul | Turkey |Norway :
Norway | NOrway |Romania :
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Carlow |Republic of Ireland :
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Galway |County Dublin :
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Haarlem |South Holland :
Leiden |Netherlands :
Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
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Queensland |Melbourne :
South Yarra |United Kingdom :
England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
Harrogate |South Yorkshire :
Sheffield |Oxfordshire :
Witney |Ontario :
Uxbridge | North York | Richmond Hill | Renfrew | Mississauga | Australia |Canada :
Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
Heist op den Berg |Flemish Brabant :
Zaventem |South America :
Argentina | Peru |Brazil :
Brazil | Sao paulo |Attica :
Athens | Koropi |Greece :
Greece |North Island :
Auckland |New Zealand :
New Zealand |Austria :
Austria |Vienna :
Vienna |Catalonia :
Barcelona |Madrid :
Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Estonia | Tartu |Harju County (Maakond) :
Tallinn |Hà Nội :
Hà Nội | Hanoi |Ho Chi Minh :
Ho Chi Minh City |Italy :
Italy |Lombardy :
Rho |Jakarta :
Jakarta |East Java :
Surabaya |Japan :
Japan | Saitama |Tokyo :
Otemachi |North Ostrobothnia :
Oulu |Southwest Finland (Varsinais-Suomi) :
Turku |Remote Korea :
Remote Korea |Republic of Korea :
Seoul |Kazakhstan :
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New Mexico | Ciudad de México |Dubai :
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Rabigh | Jeddah | Najran | King Abdullah Economic City | Riyadh | Khulais |Kuala Lumpur :
Kuala Lumpur |Kyiv Oblast :
Kyiv |Lima Region :
Lima |France :
Lyon | Paris |South Africa :
South Africa | Midrand |Nišava District :
Niš |Bohemia :
Prague |Chile :
Santiago |Bosnia and Herzegovina :
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