Medical Review Scientist (Drug Safety) – Remote
Company: ICON Strategic Solutions
Location: Philippines (Home-Based / Remote)
Employment Type: Full-Time
Experience Level: Mid to Senior Level
Experience Required: 3–7+ Years
Start Date: 28 December 2025
Application Deadline: 27 January 2026
Salary: Competitive (Based on experience and qualifications)
About ICON Strategic Solutions
ICON plc is a global leader in healthcare intelligence and clinical research, supporting pharmaceutical, biotechnology, and medical device companies in bringing innovative therapies to patients worldwide. ICON is committed to scientific excellence, regulatory compliance, and patient safety, supported by a diverse and inclusive global workforce.
Role Overview
ICON Strategic Solutions is seeking a Medical Review Scientist (Drug Safety) to join its Global Patient Safety team in a home-based role in the Philippines. This position plays a critical role in the medical review of safety data, ensuring high-quality pharmacovigilance activities and regulatory compliance across clinical trials and post-marketing programs.
The Medical Review Scientist will provide medical expertise in the review of Individual Case Safety Reports (ICSRs), collaborate cross-functionally, and contribute to risk management and safety surveillance strategies across multiple therapeutic areas.
Key Responsibilities
Perform comprehensive medical review and assessment of Individual Case Safety Reports (ICSRs) from clinical trial and post-marketing sources
Ensure accuracy, medical validity, and regulatory compliance of safety case reports within global timelines
Conduct medical evaluation of adverse events, seriousness, expectedness, and causality across therapeutic areas
Collaborate with cross-functional teams within Global Patient Safety, Clinical Operations, and Regulatory Affairs
Support development and execution of risk management strategies and risk minimization activities
Contribute to safety-related documents, including Periodic Safety Update Reports (PSURs), DSURs, and Risk Management Plans (RMPs)
Monitor emerging safety signals, medical literature, and regulatory updates to support proactive safety surveillance
Provide technical input and medical leadership within Case Management and broader pharmacovigilance teams
Support audits, inspections, and regulatory inquiries related to drug safety activities
Qualifications & Experience Required
Education & Licensure
Medical degree (MD or equivalent) with an active medical license
Board certification or equivalent clinical experience in a relevant specialty (e.g., Internal Medicine, Pharmacology, or related disciplines) preferred
Experience
Minimum 3–7 years of experience in pharmacovigilance, drug safety, or clinical safety roles within the pharmaceutical, biotech, or CRO industry
Hands-on experience with ICSR medical review and global safety reporting requirements
Familiarity with international regulatory guidelines (ICH, GCP, FDA, EMA)
Skills & Competencies
Strong clinical judgment and analytical skills with the ability to interpret complex safety data
Excellent written and verbal communication skills
Proven ability to collaborate effectively within cross-functional and global teams
High attention to detail, scientific rigor, and commitment to patient safety
Ability to manage multiple priorities in a fast-paced, regulated environment
Why Join ICON?
Fully remote, home-based role in the Philippines
Opportunity to work on global clinical development and pharmacovigilance programs
Competitive compensation and comprehensive benefits package
Strong focus on employee well-being, work-life balance, and career development
Inclusive, high-performance culture driven by scientific excellence
ICON Strategic Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status, or any other protected characteristic.
Apply now on thepharmadaily.com to advance your career in drug safety and medical review with a global clinical research leader.
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Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Detroit | Houghton Lake | Macomb | Southfield |North Dakota :
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Frank Scottile Blvd |Missouri :
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Copenhagen | Denmark |Europe :
Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Istanbul | Turkey |Norway :
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Harrogate |South Yorkshire :
Sheffield |Oxfordshire :
Witney |Ontario :
Richmond Hill | Mississauga | Uxbridge | Australia | North York | Renfrew |Canada :
Canada |Quebec :
Montreal |Brussels :
Brussels |Antwerp :
Heist op den Berg |Flemish Brabant :
Zaventem |South America :
Argentina | Peru |Brazil :
Sao paulo | Brazil |Attica :
Koropi | Athens |Greece :
Greece |North Island :
Auckland |New Zealand :
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Austria |Vienna :
Vienna |Catalonia :
Barcelona |Madrid :
Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Tartu | Estonia |Harju County (Maakond) :
Tallinn |Hà Nội :
Hà Nội | Hanoi |Ho Chi Minh :
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Italy |Lombardy :
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Oulu |Southwest Finland (Varsinais-Suomi) :
Turku |Remote Korea :
Remote Korea |Republic of Korea :
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Kyiv |Lima Region :
Lima |France :
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Santiago |Bosnia and Herzegovina :
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