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Healthcare
› Clinical Project Mgmt
Clinical Project Mgmt
1,381 open positions
Clinical Lead Project Manager
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Psi Cro
Remote
€93k
15d
Lead full-service global clinical research projects from startup to closure, managing multi-center studies across various therapeutic areas.
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Principal Data Team Lead, EMEA
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Iqvia
Dublin, County Dublin, Ireland
15d
Lead end-to-end delivery of Clinical Data Management (CDM) services for global clinical trials, ensuring quality deliverables on time and within budget for life sciences clients.
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Senior Clinical Project Manager
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RBW Consulting
€80k–€90k
15d
Managing clinical trials to ensure timely delivery of project objectives, adherence to timelines within budget parameters, and compliance with client agreements and regulations.
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Clinical Trials Manager
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Ona Therapeutics
15d
Lead the initiation, execution, oversight, and closure of early-phase oncology clinical trials for antibody drug conjugates (ADCs) and monoclonal antibodies, managing CROs, vendors, and clinical sites to ensure adherence to protocols and timelines.
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Team Lead, PCS
↗
ICON Plc
Barcelona, Catalonia, Spain
15d
Oversee a team of project and operations staff within the Language Services department, ensuring high standards in training, risk management, and resource allocation for clinical/pharmaceutical localization.
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Senior Clinical Study Manager
Cycle Pharmaceuticals
Cambridge
15d
Manage operational delivery of Phase 3 clinical trials and Phase 4 post-approval studies for rare diseases, ensuring delivery to agreed timelines, budgets, and regulatory compliance.
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Clinical Project Manager
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RBW Consulting
€70k–€80k
15d
Manage clinical trials to ensure timely delivery of project objectives, adherence to timelines within budget parameters, and compliance with client agreements and regulations.
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Local Trial Manager, Sponsor Dedicated → Responsable local(e) des essais cliniques, dédié(e) au promoteur
Iqvia
Kirkland, Quebec, Canada
15d
Local management of clinical trials within assigned countries, ensuring studies are conducted in accordance with protocol requirements, applicable regulations, and ICH-GCP guidelines.
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Study Delivery Lead NIS
↗
ICON Strategic Solutions
15d
Lead and drive cross-functional teams to deliver high-quality Non-Interventional Studies (NIS) including prospective/retrospective designs, real-world evidence, and economic modelling.
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Evidence Delivery Associate/Manager, Medical Evidence Canada
↗
Brunel
Mississauga, Ontario, Canada
15d
Lead the strategic and efficient delivery of externally sponsored research (ESR) studies and manage real-world evidence (RWE) operations for clients in Oncology and Biopharmaceuticals.
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Operations Senior Project Manager
↗
Novartis Ireland
Dublin, County Dublin, Ireland
€76k
15d
Partner with Site Management and Monitoring leadership to drive strategic resource planning, budget management, and data-driven decision-making for global clinical operations.
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Project Manager, Vendor Management / Gestionnaire de projet, gestion des fournisseurs
↗
Indero (formerly Innovaderm)
Montreal, Quebec, Canada
15d
Manage clinical research projects and oversee study-specific vendors throughout the lifecycle, ensuring compliance with GCP, regulatory requirements, and project timelines.
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Operations Senior Project Manager
↗
Novartis
Barcelona, Catalonia, Spain
€64k–€118k
15d
Partner with Site Management and Monitoring leadership to drive strategic resource planning, budget management, and data-driven decision-making for global clinical operations.
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Clinical Operations Manager-Traveling CRC Team
↗
Activmed Practices & Research, LLC.
Burlington, Ontario, Canada
15d
Manage and execute clinical research support across multiple site locations, ensuring patient safety, protocol compliance, and study milestones are met.
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Ophthalmology Sr. Clinical Research Associate
↗
Bayside Solutions
Remote
$104k–$125k
15d
Lead a team of Clinical Research Associates (CRAs) and Clinical Trial Associates (CTAs) to oversee the initiation, enrollment, conduct, and completion of ophthalmology clinical trials.
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Global Clinical Project Manager - Vendor Management Expert (home-based in Europe)
↗
Iqvia
Remote
15d
Manage vendor activities across the study lifecycle for global clinical trials (Phase I–IV), ensuring timely and high-quality deliverables for central lab, eCOA, IRT, ECG, Imaging, Ancillaries, and/or Patient Recruitment & Retention.
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Clinical Research Project Manager
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Hiring Specialist | Bfsi • Fintech • AI • Technology Recruitment
Ahmedabad, Gujarat, India
15d
Managing global clinical research projects from start-up to close-out, ensuring delivery within timelines, budgets, and quality standards.
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Director, US Head of HOCT Trial Management, Clinical Operations
Bms
Princeton - NJ - US
$213k–$258k
15d
Lead the HOCT Clinical Trial Management team for Regional Clinical Operations in North America, ensuring effective execution of clinical trials across the BMS R&D portfolio.
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Senior Director, Clinical Trials Performance & Head of Operations, SPHERE CRO
↗
Healthcarecan
Toronto, ON, CA
15d
Lead the execution of clinical trials strategy, build the Central Clinical Trials Unit, and oversee the financial and operational performance of SPHERE CRO.
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Mgr Site Payments - FSP
↗
Thermo Fisher Scientific
15d
Lead a high-performing team to deliver end-to-end Investigator Payments Management for global clinical trials, ensuring accurate, compliant, and timely payments.
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Clinical Trial Manager UK/EU
↗
Kps Life
Remote
15d
Lead cross-functional study teams to deliver clinical research study deliverables on time, within budget, and with good quality in compliance with Regulatory Authorities' regulations/ICH GCP guidelines.
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Clinical Operations Lead
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Incyte Corporation
Remote, US
15d
Supports the Clinical Trial Manager and operational team in executing clinical trials for biopharmaceutical products.
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Senior Clinical Trial Manager
↗
Incyte Corporation
Remote, US
15d
Manage multinational clinical trials from initiation to study report, overseeing timelines, budgets, site selection, vendor coordination, and patient recruitment for biopharmaceutical products.
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Sr. Principal I, Clinical Project Management
Alcon
Fort Worth, Texas, US
15d
Global/regional clinical expert responsible for planning, organizing, and executing clinical projects from development to post-market monitoring for ophthalmic products.
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FSP Principal CTC
Thermofisher
Ciudad de Mexico, Mexico
15d
Principal Clinical Trial Coordinator providing administrative and technical support to project teams, overseeing study administration, site activation, and process improvement for clinical trials.
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Site Contract Specialist
Medpace
São Paulo, Brazil
16d
Managing site contract agreements, budgets, and negotiations to advance clinical trial start-up and execution.
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Manager, Central Monitor-Hybrid
AbbVie
North Chicago, IL, us
16d
Managing a global team of central monitors to execute risk-based quality monitoring (RBQM) for clinical research studies, ensuring on-time delivery with quality and efficiency across multiple therapeutic areas.
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Clinical Site Relationships Coordinator
Medpace
Tokyo, Japan
16d
Build and maintain relationships with Site Management Organizations (SMOs) to support clinical trial feasibility, site selection, and study start-up in Japan.
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Manager, Quality Clinical Risk Management
Johnson and Johnson
Beerse, Turnhout
16d
Lead clinical quality-risk management across trials and programs, translating risk signals into proactive mitigation and ensuring inspection readiness.
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Assoc. Manager / Manager, Clinical Operations - FSP
Thermofisher
Remote, California, USA
$115k–$180k
16d
Oversee, train, resource, and coach a team of clinical operations staff dedicated to a single sponsor, ensuring adherence to SOPs and WPDs while driving performance via metrics.
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Contract Manager
Thermofisher
Remote, Malaysia
16d
Regional lead managing preparation, negotiation, and finalization of contract templates, process parameters, and investigator grant budgets for clients in the clinical research industry.
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Sr ICF Medical Writing Project Manager
Thermofisher
Remote, Serbia
16d
Lead ambitious initiatives to craft the future of clinical research by delivering flawless Informed Consent Forms (ICFs) and other critical documents, ensuring outstanding quality and compliance.
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Clinical Project Manager
↗
Everest Clinical Research
Remote
16d
Manage clinical research projects (Phase I-IV) for pharmaceutical, biotechnology, and medical device clients, ensuring timely delivery, budget adherence, and regulatory compliance.
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Associate Director, Project Management
↗
Everest Clinical Research
Remote
16d
Lead project planning, communication, and execution for clinical research and development services, overseeing Project Managers and ensuring quality deliverables across multiple clinical development programs.
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Project Manager [Lead CRA]
↗
Remoto, BR
16d
Manage all clinical research project activities for a CRO and contribute to internal team training.
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Site Contract Specialist
↗
Medpace
São Paulo, SP, BR
16d
Full-time Contract Specialist supporting clinical trial study start-up and management by preparing, negotiating, and finalizing site agreements and budgets.
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Start-up Manager, FSP
↗
Thermo Fisher Scientific
16d
Manage complex site operations, ensure regulatory compliance, and facilitate collaboration between trial sites and internal teams to drive clinical study success.
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Manager, Clinical Operations
↗
ICON Strategic Solutions
Chennai, Tamil Nadu, India
16d
Oversee the execution of clinical trials, ensuring they are conducted efficiently, on time, and in compliance with regulatory requirements.
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Sr. CTM - FSP
↗
Thermo Fisher Scientific
16d
Lead Local Study Team(s) at country level to deliver committed components of clinical studies, ensuring site identification, qualification, monitoring, and data delivery to required quality.
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FSP Associate Manager Clinical Operations - Germany (m/f/d)
Thermofisher
Remote, Germany
16d
Oversees daily line management and performance of clinical operations teams (CAS, CS, CRAs, RSMs, PAs) in monitoring environments (FSO, FSP, Government), ensuring adherence to SOPs and WPDs.
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Sr Project Manager, FSP
↗
Thermo Fisher Scientific
16d
Lead cross-functional projects in biomedical/life sciences, ensuring delivery of quality, time, and cost objectives for multi-service, multi-region, or complex therapeutic initiatives.
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ICU Clinical Research Manager 1
↗
Royal Melbourne Hospital
Parkville, VIC, AU
16d
Lead and manage clinical research activities, trials, and governance within the Intensive Care Unit (ICU), supporting high-quality patient care and research delivery.
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Director Global Oncology Medical Affairs Clinical Operations (m/f/d)
↗
Daiichi Sankyo Europe GmbH
Munich, Bavaria, Germany
16d
Lead operational strategy and execution of global company-sponsored interventional and non-interventional studies and medical affairs research projects in oncology.
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Senior Clinical Specialist
↗
EPM Scientific
San Mateo County, CA
16d
Senior Clinical Specialist supporting global clinical studies from site start-up through close-out for a clinical-stage biopharmaceutical company.
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Senior Clinical Research Associate
↗
BioTalent
Remote
$140k
16d
Lead and oversee a team of Clinical Research Associates (CRAs) supporting a complex, multi-site clinical trial across the United States, ensuring consistent monitoring practices and operational efficiency.
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Sr Manager, Clinical Trial Lead
Biibhr
Cambridge, MA, US
$141k–$188k
16d
Leading operational planning, execution, and delivery of clinical studies across the development lifecycle, managing timelines, budgets, and CRO partnerships.
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ICU Clinical Research Manager 1
↗
The Royal Melbourne Hospital
Melbourne, Victoria, Australia
16d
Lead and manage clinical research activities, trials, and governance within the Intensive Care Unit (ICU), supporting high-quality patient care and research delivery.
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Associate Director, Clinical Operations Program Lead, Study Start-up & Feasibility
Sarepta
Cambridge, MA, US
$161k–$201k
16d
Lead strategy and implementation of country and site feasibility and study start-up for clinical trials in rare diseases.
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Sr. Project Manager, FSP
↗
Thermo Fisher Scientific
16d
Lead cross-functional projects in biomedical/life sciences, ensuring delivery of quality, time, and cost objectives while managing sponsor expectations and financial stewardship.
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Study Manager
↗
Talentmark
Welwyn Garden City, England, UK
16d
Provide operational expertise into protocol design, feasibility, country selection, and data delivery plans for clinical studies.
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