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Healthcare
› Clinical Project Mgmt
Clinical Project Mgmt
1,393 open positions
Sr Site Contract Specialist
Thermofisher
Warsaw, Poland
1mo
Prepare, negotiate, and finalize contracts with clinical study sites to ensure efficient site activation and compliance with client and local processes.
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Associate Director, Local Delivery Lead/Local Trial Manager
Gsk
Remote
$130k
1mo
End-to-end leadership for US clinical study delivery, serving as the primary operational link between global study teams and local US operations for a portfolio of oncology studies.
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Strategic Site Partner
AbbVie
North Chicago, IL, us
1mo
Develops holistic strategy and global network of Principal Investigator (PI) and institution partnerships to accelerate AbbVie's solid tumor and hematology clinical trial pipelines.
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Region Manager
Careaccess
Remote
$95k–$115k
1mo
Lead operations and performance of multiple clinical research sites to ensure successful execution of clinical trials in compliance with regulatory guidelines.
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Strategic Site Partner
AbbVie
Shanghai, Shanghai, cn
1mo
Develops holistic strategies and manages global networks of clinical sites to accelerate AbbVie's solid tumor and hematology drug pipelines.
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Negotiation Governance Lead
Bristolmyerssquibb
Warsaw-WeWork-PL
251k
1mo
Leads complex site contract and budget negotiations for global clinical trial agreements, ensuring legal and budget governance while driving efficiencies in site activation.
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Gestionnaire de l’activation des sites/ Site Activation Manager
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Iqvia
Remote
1mo
Lead and manage the strategic, operational, and financial execution of site activation activities, including site selection, regulatory processes, and contract negotiation for assigned clinical studies.
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Clinical Trial Manager - Spain (Madrid) - Infectious Disease / Immunology
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Medpace
Madrid, Community of Madrid, Spain
1mo
Manage day-to-day operations of clinical trials for biotech and pharmaceutical companies, ensuring compliance with ICH/GCP and applicable regulations.
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Senior Contract Specialist
Thermofisher
Bucharest, Romania
1mo
Manages the preparation, negotiation, and finalization of Investigator Contracts with study sites, ensuring quality, objectivity, and risk analysis.
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Global Lead Project Manager (FSP), Costa Rica (Remote)
Thermofisher
Remote
1mo
Lead cross-functional clinical trial projects from initiation to completion, ensuring delivery of quality, time, and cost objectives while managing vendor oversight and customer expectations.
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(Associate) Country Study Manager - CVRM
AstraZeneca
Beijing Yizhuang, CN
1mo
Lead the end-to-end delivery of clinical studies from planning through closeout, ensuring compliance with local regulations and ICH-GCP standards while managing local study teams and regulatory submissions.
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Negotiation Governance Lead
Bms
Warsaw-WeWork-PL
251k
1mo
Leads complex site contract and budget negotiations for global clinical trial agreements, ensuring legal and budget governance while implementing fallback standards.
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Associate Manager, Clinical Imaging Operations
Regeneron
TARRYTOWN, US
$110k
1mo
Manage operational aspects of early and late phase clinical trials for general medicine imaging modalities (US, MRI, DXA, CT, photography) to ensure high-quality image acquisition and data integrity.
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Associate Director, Clinical Supply Chain, Cambridge, MA
Isomorphiclabs
Cambridge, MA
1mo
Lead end-to-end clinical trial material (CTM) planning, vendor management, packaging, labeling, inventory management, and global distribution operations for investigational products.
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Site Contract Specialist (Based in Shanghai)
Medpace
Shanghai, China
1mo
Liaison between Sponsor, investigative sites, and Medpace to negotiate contracts and budgets for clinical trial start-up.
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Regulatory Submissions Manager
Medpace
Taipei, Taiwan
1mo
Manage and execute global clinical study start-up submissions, ensuring document quality and regulatory compliance for new trials.
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Associate Director, Regulatory Submissions
Medpace
South Yarra, Melbourne, Australia
1mo
Lead the Study Start-Up group in the APAC region, driving strategic development, process improvement, and client relationships for clinical trial initiation.
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Study Start up Submissions Manager (Remote based in Delhi)
Medpace
India
1mo
Manage clinical trial startup submissions to Indian regulatory agencies (DCGI/CDSCO) and facilitate face-to-face consultations.
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(Senior) Site Contract Specialist/Manager
Medpace
Beijing, China
1mo
Liaison between Sponsor, investigative sites, and Medpace to negotiate contracts and budgets, ensuring timely project start-up.
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Regulatory Submissions (Study Start-up) Manager
Medpace
Seoul, Korea, South
1mo
Manage regional study start-up submissions and liaise with local authorities (MFDS) to expedite clinical trial approvals in the APAC region.
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Regulatory Submissions (Study Start-up) Manager
Medpace
South Yarra, Melbourne, Australia
1mo
Lead global project start-up and regulatory submissions for innovative therapies in the biotechnology, pharmaceutical, and medical device industries.
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Junior Site Contract Specialist
Medpace
South Yarra, Melbourne, Australia
1mo
Liaison between Sponsor, investigative sites, and Medpace to negotiate contracts and budgets.
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Start Up Lead APAC
Precision for Medicine
Singapore
1mo
Lead global site start-up activities for clinical trials in the APAC region, ensuring timely activation and regulatory compliance.
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Senior Strategic Outsourcing Manager
Roche
South San Francisco, US
$148k
1mo
Drive nonclinical outsourcing strategy for drug development, managing the selection and performance of Contract Research Organizations (CROs) for in-vivo and in-vitro toxicological and pharmacokinetic studies.
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Senior Clinical Trial Manager
Galderma
London, GB
1mo
Planning and managing global clinical trials to ensure delivery on timelines, budget, and quality standards while overseeing external partners.
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Clinical Program Quality Excellence Lead - FSP Team
Thermofisher
Remote, North Carolina, USA
1mo
Lead cross-functional teams in GCP inspection readiness, TMF quality strategies, and compliance monitoring for global clinical studies.
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Project Manager/Senior Project Manager - EMEA - General Medicines
↗
ICON Plc
Reading, England, UK
1mo
Leading and coordinating clinical project activities within the Biotech General Medicine portfolio to deliver studies on time, within budget, and to high quality standards.
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Study Start Up Manager
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Medpace
1mo
Manage and execute all aspects of global clinical trial start-up, ensuring regulatory compliance and site readiness for LATAM regions.
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Manager - TMF Operations
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ICON Plc
Chennai, Tamil Nadu, India
1mo
Oversee the management, maintenance, and compliance of the Trial Master File (TMF) for clinical research studies.
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Director, Clinical Trial Success - CEE
Iterativehealth
IH – Remote (Ex-US Poland)
$400k
1mo
Director leading clinical trial success for sponsors and CROs across Central and Eastern Europe, ensuring effective study launches, site performance tracking, and risk resolution.
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Supply Chain Specialist
Medpace
Cincinnati, Ohio
1mo
Manage supply chain operations for clinical trials by identifying vendors, aligning lead times with study timelines, and ensuring product delivery meets clinical trial deliverables.
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Study Start-Up Project Manager
Medpace
Denver, Colorado
$100k
1mo
Manage the full lifecycle of clinical trial start-up, maintenance, and close-out, serving as the primary contact for regulatory submissions and business development proposals.
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Supply Chain Manager
Medpace
Cincinnati, Ohio
1mo
Lead supply chain design and management processes to streamline the startup and execution of clinical trials, overseeing sourcing, purchasing, and fulfillment activities.
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Study Start-Up Project Manager
Medpace
Cincinnati, Ohio
1mo
Manage the full lifecycle of clinical trial start-up, maintenance, and close-out for biopharma clients.
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Experienced Study Start-Up Project Manager (Remote)
Medpace
Remote
1mo
Manage the global execution of clinical trial start-up, maintenance, and close-out processes to accelerate the development of medical therapeutics.
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Clinical Supply Chain Project Specialist (PharmD Candidates)
Medpace
Cincinnati, Ohio
1mo
Manage the supply chain for investigational products in clinical trials, translating study protocols into actionable logistics and ensuring timeline alignment.
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Clinical Trial Manager (Neuroscience/CNS)
Medpace
South Yarra, Melbourne, Australia
1mo
Lead multiservice global/regional clinical trials for biotechnology, pharmaceutical, and medical device clients, managing timelines, deliverables, and cross-functional teams from startup to closure.
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Expanded Access Manager / Post-Trial Access Specialist - FSP - UK
Thermofisher
Remote, United Kingdom
1mo
Operational leadership for managed access programs (compassionate use, expanded access, post-trial access) in oncology, ensuring continuity of investigational product supply and regulatory compliance for patients after clinical trials.
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Clinical Trial Manager
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Fortrea
Remote
$76k–$148k
1mo
End-to-end oversight of clinical trial start-up and clinical delivery, managing site activation, regulatory submissions, and operational compliance from site identification to database lock.
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Regional Study Start-Up Lead
Biibhr
Baar, Switzerland
1mo
Lead regional site activation and study start-up operations for clinical trials across European countries, ensuring timely site selection, regulatory submissions, and operational readiness.
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Global Study Manager - FSP - UK - PACT/MAP experience
Thermofisher
Remote, United Kingdom
1mo
End-to-end operational delivery of global clinical studies from initiation to archiving, ensuring robust plans and quality delivery for a leading bio-pharma company.
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Project Manager, Accellacare
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ICON Plc
Remote
1mo
Lead and manage the planning, execution, and monitoring of single service global projects within the Accellacare clinical research network.
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Clinical Trial Manager (Neuroscience/CNS)
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Medpace
South Yarra, Victoria, Australia
1mo
Lead multiservice global/regional clinical trials from startup to database lock and closure, coordinating all contracted services and managing the cross-functional team.
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Start Up Lead APAC
↗
Precision for Medicine
1mo
Lead global site start-up activities for clinical trials in the APAC region, managing strategy, planning, and coordination to ensure timely site activation.
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Local Study Associate Director- FSP
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Parexel
Remote
1mo
Leads Local Study Teams at the country level to deliver clinical study components, manage site selection/qualification, and ensure compliance with ICH-GCP and local regulations.
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Global Sr Project Manager - FSP
↗
Thermo Fisher Scientific
1mo
Global Study Lead responsible for end-to-end management of a global clinical study for a bio-pharma company, ensuring alignment between global strategy and regional execution.
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Associate Director Clinical Project Management
Join The CTI Team
Sydney, New South Wales
1mo
Plan, implement, and evaluate the full execution of assigned clinical trials from planning to analysis, ensuring compliance with ICH/GCP guidelines and managing global trial activities for pharmaceutical and biotechnology clients.
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Medical Doctor / MBBS Career Event: Clinical Trial Management – Medpace London
Medpace
London, United Kingdom
1mo
Associate Clinical Trial Manager supporting global clinical trial operations, coordinating study activities, and managing regulatory filings and supplies for biopharma clients.
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Research Budget Specialist - Cardiology
Iterativehealth
IH – Boston (Cambridge)
1mo
Develop, review, and negotiate site-level clinical trial budgets and payment terms with sponsors and CROs for U.S. and international research sites.
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Sr. Director, Clinical Operations
Flagshippioneeringinc
Metaphore Biotechnologies, Inc.
1mo
Lead hands-on execution of early clinical development activities, specifically first-in-human Phase 1 studies, for a biological therapeutics company.
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