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Healthcare
› Clinical Project Mgmt
Clinical Project Mgmt
803 open positions
Manager, Clinical Outcome Assessment Digital Implementation Team Navigator
AbbVie
North Chicago, IL, us
1d
Strategic lead for Clinical Outcome Assessment (COA) licensing, translation, and implementation across therapeutic areas, driving early stakeholder alignment and end-to-end delivery.
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Specialist, Country Study Start Up
AbbVie
Maidenhead, England, gb
1d
Proactively drives and executes all start-up and maintenance activities and deliverables for assigned clinical studies and sites in a specific country.
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Manager/Senior Manager, Clinical Supply Chain
Jobgether
Remote
$115k–$115k
1d
Oversees clinical drug supply activities across development programs to ensure patients receive accurate and continuous supplies.
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(Senior) Site Contract Specialist/Manager
Medpace
Beijing, China
1d
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
1d
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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Associate Director, Regulatory Submissions
Medpace
South Yarra, Melbourne, Australia
1d
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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Junior Site Contract Specialist
Medpace
South Yarra, Melbourne, Australia
1d
Liaison between Sponsor, investigative sites, and Medpace to negotiate contracts and budgets.
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Study Start up Submissions Manager (Remote based in Delhi)
Medpace
India
1d
Manage clinical trial startup submissions to Indian regulatory agencies (DCGI/CDSCO) and facilitate face-to-face consultations.
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Site Contract Specialist (Based in Shanghai)
Medpace
Shanghai, China
1d
Liaison between Sponsor, investigative sites, and Medpace to negotiate contracts and budgets for clinical trial start-up.
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Regulatory Submissions (Study Start-up) Manager
Medpace
South Yarra, Melbourne, Australia
1d
Lead global project start-up and regulatory submissions for innovative therapies in the biotechnology, pharmaceutical, and medical device industries.
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Regulatory Submissions Manager
Medpace
Taipei, Taiwan
1d
Manage and execute global clinical study start-up submissions, ensuring document quality and regulatory compliance for new trials.
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Project Leader
Jobgether
Remote
1d
Lead end-to-end delivery of complex clinical research projects and trials to support new therapy development and patient outcomes.
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BPM Evidence Associate (fixed term/secondment)
AstraZeneca
Poland - Warsaw
1d
Coordinate and support the operational delivery of global strategic studies, including company-sponsored research, externally sponsored research, and early access programs, to generate evidence for AstraZeneca therapies.
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Senior Operations Manager – Clinical Research
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Sunshine Group
MH, IN
$960k–$960k
1d
Manage clinical research operations across multiple studies and sites, overseeing start-up, activation, conduct, closeout, and documentation.
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RTSM Project Manager (Randomisation and Trial Supply Management)
Gsk
UK - Hertfordshire - Stevenage
$72k–$120k
1d
Design, develop, test, validate, execute, and maintain clinical studies within the RAMOS IRT (Interactive Response Technology) system, ensuring data integrity and driving continuous improvement across clinical supply systems.
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Director, US Portfolio Delivery (cross-TA)
Gsk
Home Worker - USA
$154k–$154k
1d
Provides leadership and oversight for the delivery of clinical studies in the US to support global R&D programs for vaccines and medicines.
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CBI - Biospecimen Lead (BSL)
Bristolmyerssquibb
Warsaw-WeWork-PL
$219k–$219k
1d
Manage biospecimen operations for 5-12 clinical trials, developing management plans and ensuring data delivery timelines.
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Senior Trial Supplies Manager
Bristolmyerssquibb
Hyderabad - TS - IN
1d
Create and maintain supply strategies for investigational products to support global clinical studies in oncology, hematology, immunology, and cardiovascular disease.
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Associate Site Activation Manager
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Iqvia
Remote
1d
Lead global study start-up and site activation activities to accelerate patient enrolment and ensure on-time delivery of clinical trials.
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Clinical Program Quality Excellence Lead - FSP Team
Thermofisher
Remote, North Carolina, USA
1d
Lead cross-functional teams in GCP inspection readiness and execution throughout the clinical study lifecycle, ensuring high-quality deliverables and TMF performance.
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Associate Director, Country & Site Operations FSP Oversight Manager
Biibhr
Remote, USA
$171k–$171k
1d
Manage and oversee Functional Service Provider (FSP) staff to support country- and site-level clinical trial execution, ensuring operational consistency and efficiency across regions.
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Global Study Leadership - Clinical Lead - Oncology
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Iqvia
Remote
1d
Lead clinical delivery of regional and global oncology studies, ensuring recruitment, site performance, quality, and operational objectives are met.
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Global Study Leadership - Clinical Lead - Oncology
Iqvia
Sofia, Bulgaria
1d
Lead clinical delivery of regional and global oncology studies, ensuring recruitment, site performance, quality, and operational objectives are met.
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RTSM Study Project Lead - Level 1
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4g Clinical
Remote, US
1d
Lead client support for the Randomization and Trial Supply Management (RTSM) application after clinical study go-live, acting as the primary contact for study sponsors.
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Associate Site Activation Manager
Iqvia
Sofia, Bulgaria
1d
Lead global study start-up and site activation activities to accelerate patient enrolment and ensure on-time delivery of clinical trials.
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Clinical Project Management Director – Patient-Centered Solutions (Multiple Locations)
Iqvia
London, United Kingdom
1d
Lead operational and strategic delivery of in-trial interview (ITI) and patient experience data (PED) studies for biopharmaceutical clients.
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Clinical Operations Manager
Iqvia
Shanghai, China
1d
Manage clinical research staff, allocate resources to studies, and ensure quality compliance with regulatory standards.
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Clinical Research Engagement Lead - South Region (Miami, FL)
Roche
Miami, US
$109k–$109k
1d
Strategic partner bridging strategy and execution across the clinical trial lifecycle to build high-trust partnerships with clinical trial sites and accelerate recruitment.
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Senior Strategic Outsourcing Manager
Roche
South San Francisco, US
$148k–$148k
1d
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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Regional Supervisor, Global Operations UK/EU
Catalent
Bathgate, United Kingdom
1d
Lead regional teams to ensure effective workload management, operational excellence, and compliance in clinical supply services.
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Senior Clinical Trial Manager
Galderma
London, GB
1d
Planning and managing global clinical trials to ensure delivery on timelines, budget, and quality standards while overseeing external partners.
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Senior Clinical Project Manager
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Nestlé USA
Jurong, S00, SG
1d
Manage the operational phase of clinical trials to ensure timely delivery of quality data while complying with GCP guidelines and internal SOPs.
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Resource Analyst Supporting Integrated Data Services (Biostatistics, Programming, & Data Management)
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Thermo Fisher Scientific
Desde casa, MX
2d
Forecast, track, and allocate clinical resources (biostatisticians, programmers, data managers) for global clinical research projects to ensure efficient utilization and profitability.
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Resource Analyst Supporting Integrated Data Services (Biostatistics, Programming, & Data Management)
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Thermo Fisher Scientific
São Paulo, SP, BR
2d
Forecast, track, and identify resource allocation needs and assignments for clinical projects to ensure efficient labor utilization and team composition.
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Associate Mgr - Centralized Monitoring (Line Manager)
IQVIA India
India
3d
Supervise and manage a team of project delivery support staff to ensure timely, high-quality completion of clinical research deliverables in alignment with SOPs and customer KPIs.
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Wsparcie w Zarządzaniu Projektami Badań Klinicznych
Grupa Neuca
Warszawa, mazowieckie
3d
Independent execution and coordination of clinical research projects, ensuring adherence to schedules, scope, and quality requirements while managing cross-functional teams.
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Sr. Project Management Analyst
Iqvia
Centurion, Tshwane
3d
Sr. Project Management Analyst driving project management activities for clinical trials to mitigate risk, control cost, and manage schedules.
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Client Services Project Manager.
Iqvia
Remote
3d
Manages and validates scope, plans, and schedules for moderately complex eCOA (electronic Clinical Outcome Assessment) studies, serving as the primary client contact for live and maintenance projects.
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Senior Manager, Clinical Supply, Pulmovant
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Remote
3d
Lead global clinical supply chain operations to ensure on-time delivery of investigational medicinal products (IMP) for Phase 3 and future trials.
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Clinical Trial Project Lead
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University of Alberta
Edmonton, AB, CA
3d
Leads and manages the overall operation, coordination, and project management of local, national, and international clinical trial projects.
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Manager, Clinical Study Operations
Beaconbiosignals
Remote
$115k–$115k
3d
Lead a team managing end-to-end execution of device-based clinical trials for neurological, psychiatric, and sleep disorder therapeutics and diagnostics.
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Clinical Operations Manager
AbbVie
São Paulo, SP, br
3d
Lead high-performing clinical research teams to accelerate AbbVie's pipeline and bring innovative therapies to patients.
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Study Start-Up Project Manager
Medpace
Denver, Colorado
$100k–$100k
4d
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 Specialist
Medpace
Cincinnati, Ohio
4d
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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Supply Chain Manager
Medpace
Cincinnati, Ohio
4d
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
4d
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
4d
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
4d
Manage the supply chain for investigational products in clinical trials, translating study protocols into actionable logistics and ensuring timeline alignment.
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Senior Scientist I/II - Outsourcing Manager, Analytical R&D
AbbVie
North Chicago, IL, us
4d
Single point of contact for internal project teams and external service providers, strategically coordinating global outsourcing activities for early-phase development projects in formulation, manufacturing, and analytics.
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Clinical Trial Manager (Neuroscience/CNS)
Medpace
South Yarra, Melbourne, Australia
4d
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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