Job Title: Trial Delivery Specialist – Clinical Trial Coordination
Location: Remote, India
Employment Type: Full-time, Fully Remote
Job ID: R-01329124
Our client, a leading global biopharmaceutical company, is seeking a Trial Delivery Specialist to ensure operational excellence in clinical trial management across all phases and therapeutic areas. As an embedded FSP study delivery partner, you will act as an extension of the global study team, overseeing trial coordination, vendor management, and data integrity to support high-quality study delivery.
This role provides a unique opportunity to work on global clinical studies, gain exposure to cutting-edge clinical trial technologies, and contribute to bringing life-changing medicines to patients worldwide.
Collaborate with global study leaders to monitor study conduct, progress, and risks, ensuring timelines, budgets, and quality objectives are met.
Oversee end-to-end operational study activities, including study set-up, project planning, system/database maintenance, and archival.
Support the development and review of study plans, monitoring plans, vendor management plans, protocol deviation plans, and risk management strategies.
Coordinate study-related communications across internal and external teams, including regulatory, CROs, and third-party vendors.
Manage vendor oversight and CRO activities, ensuring study-specific deliverables are completed efficiently.
Oversee clinical supplies and investigational products (IP), tracking risks to continuity and implementing corrective actions.
Ensure eTMF inspection readiness, maintaining completeness and quality of all trial master file documents.
Monitor study budgets, expenses, and change orders, escalating discrepancies to study stakeholders.
Bachelor’s degree in Life Sciences, Pharmacy, or related field.
Proven experience in clinical trial coordination, study operations, or clinical research within the pharmaceutical or biotechnology industry.
Knowledge of global clinical trial processes, ICH-GCP guidelines, and vendor management.
Strong project management, analytical, and organizational skills.
Excellent communication and collaboration skills to work with cross-functional global teams.
Proficiency in clinical trial technology platforms, eTMF systems, and data management tools preferred.
Opportunity to advance along the Project Management/Study Operations track or Clinical Research Associate track.
Global exposure to multi-phase, multi-therapeutic clinical studies.
Gain experience in financial tracking, risk management, and emerging clinical trial technologies including AI platforms.
Contribute to bringing life-changing medicines to patients worldwide.
Collaborate with global teams, vendors, and CRO partners.
Full remote flexibility, with opportunities for learning, mentorship, and career progression.
Gujarat :
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Bangalore | Belgaum | Bengaluru | B.G Nagara | Bommasandra | Colorado | Czech Republic | Karnataka | Mangaluru | Mysore | Udupi |Punjab :
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Pondicherry (Puducherry) |Jharkhand :
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Siliguri |Illinois :
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Andover | Billerica | Boston | Cambridge | Devens | Lexington | Massachusetts | Medford and Somerville | Rockland |Wisconsin :
Appleton | Kenosha | Pleasant Prairie | Portage | Waukesha |United states :
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Frank Scottile Blvd |Missouri :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
Finland |Istanbul :
Istanbul | Turkey |Norway :
Norway | NOrway |Romania :
Romania |Belgium :
Wavre |Tipperary :
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Brinny | Ringaskiddy |Carlow :
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Dún Laoghaire |Galway :
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Swords |Republic of China :
Beijing |China :
China | Quarry Bay |Liaoning :
Dalian |Zhejiang :
Hangzhou |Tokiyo :
Osaka | Tokyo |Shanghai Sai :
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Wuhan |Capital of Netherland :
Amsterdam |North Brabant :
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Haarlem |South Holland :
Leiden |Netherlands :
Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
Ballina | Sydney |Republic of Western Australia :
Nedlands |Queensland :
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 :
Renfrew | Uxbridge | Richmond Hill | Australia | North York | Mississauga |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 :
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Barcelona |Madrid :
Madrid |Cebu Province :
Cebu City |Philippines :
Manila |Croatia :
Croatia |Zagreb :
Zagreb |Estonia :
Estonia | Tartu |Harju County (Maakond) :
Tallinn |Hà Nội :
Hanoi | Hà Nội |Ho Chi Minh :
Ho Chi Minh City |Italy :
Italy |Lombardy :
Rho |Jakarta :
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Surabaya |Japan :
Saitama | Japan |Tokyo :
Otemachi |North Ostrobothnia :
Oulu |Southwest Finland (Varsinais-Suomi) :
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Remote Korea |Republic of Korea :
Seoul |Kazakhstan :
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Bangkok |Israel :
Tel Aviv | Netanya | Be'Er Sheva | Kfar Saba | Yavne |Remote :
Bishop | Blue Bell | Remote - South America (Latin Americal) | Melbourne | Nairobi | Remote - Middle East | Regulatory Labeling Manager (NA and LATAM Only) | Faridabad | Ireland | Tulsa | Zaragoza | Remote - Europe | Lenexa | McFarland | Hammond | Medan | Minnesota | Remote - Africa | Riga | Victoria | Castlebar | Lousiana | Springville | French | Bountiful | Hungary | Slovakia | Leinster | Remote, USA | Green Way | Remote | Thailand | Switzerland | Manipal | Xzagreb | Texas | Belgium |Republic of Colombia :
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Ciudad de México | New Mexico |Dubai :
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Najran | Jeddah | Rabigh | Khulais | King Abdullah Economic City | Riyadh |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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