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Nurse property manager

119 property manager jobs found

Professional Diversity Network
Mar 25, 2026  
Senior Study Manager, Clinical Research Operations - Ophthalmology
Merck Job Description This position leads the operational planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities : Responsible for the operational planning, feasibility, and execution of a clinical trial. May serve as the clinical trial team lead. May lead team in key study planning, development, and execution elements (e.g., data management deliverables, trial level plans/timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, preparation of status update reports, study close out activities). Leads team for timeline management, risk identification and mitigation, issue resolution. May...
Professional Diversity Network Rahway, NJ, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Senior Study Manager, Clinical Research Operations - Ophthalmology
Merck Job Description This position leads the operational planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities : Responsible for the operational planning, feasibility, and execution of a clinical trial. May serve as the clinical trial team lead. May lead team in key study planning, development, and execution elements (e.g., data management deliverables, trial level plans/timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, preparation of status update reports, study close out activities). Leads team for timeline management, risk identification and mitigation, issue resolution. May...
Professional Diversity Network Boston, MA, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Senior Study Manager, Clinical Research Operations - Ophthalmology
Merck Job Description This position leads the operational planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities : Responsible for the operational planning, feasibility, and execution of a clinical trial. May serve as the clinical trial team lead. May lead team in key study planning, development, and execution elements (e.g., data management deliverables, trial level plans/timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, preparation of status update reports, study close out activities). Leads team for timeline management, risk identification and mitigation, issue resolution. May...
Professional Diversity Network North Wales, PA, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Senior Study Manager, Clinical Research Operations - Ophthalmology
Merck Job Description This position leads the operational planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities : Responsible for the operational planning, feasibility, and execution of a clinical trial. May serve as the clinical trial team lead. May lead team in key study planning, development, and execution elements (e.g., data management deliverables, trial level plans/timelines, country/site selection, site materials, system updates, investigator meeting planning, communication plans, preparation of status update reports, study close out activities). Leads team for timeline management, risk identification and mitigation, issue resolution. May...
Professional Diversity Network Philadelphia, PA, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Senior Scientist, Clinical Research Operations - Ophthalmology
Merck Job Description This position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership, technical skills, and scientific acumen as part of a global, cross-functional team. Job Responsibilities Responsible for leading specific aspects of clinical/scientific execution of clinical protocol(s). This may include: Serving as the lead clinical scientist on the clinical trial team. Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director. Other responsibilities include: Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data collection in alignment with the protocol in...
Professional Diversity Network Boston, MA, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Study Manager, Clinical Research Operations - Ophthalmology - Hybrid
Merck Job Description Job Summary This position contributes to the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to develop your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities May have specific operational responsibilities for asingle study or across multiple studies (e.g., operational deliverables, clinical & ancillary supplies planning/tracking, lab specimen tracking, status update reports, study closeout activities). May be responsible for tracking study timelines using project management tools. Shares technical expertise with team members. May interact with internal and external stakeholders (e.g.,study team, vendors, committees) in support of clinical trial objectives. Core Skills Working knowledge of clinical...
Professional Diversity Network Boston, MA, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Senior Scientist, Clinical Research Operations - Ophthalmology
Merck Job Description This position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership, technical skills, and scientific acumen as part of a global, cross-functional team. Job Responsibilities Responsible for leading specific aspects of clinical/scientific execution of clinical protocol(s). This may include: Serving as the lead clinical scientist on the clinical trial team. Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director. Other responsibilities include: Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data collection in alignment with the protocol in...
Professional Diversity Network Boston, MA, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Senior Scientist, Clinical Research Operations - Ophthalmology
Merck Job Description This position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership, technical skills, and scientific acumen as part of a global, cross-functional team. Job Responsibilities Responsible for leading specific aspects of clinical/scientific execution of clinical protocol(s). This may include: Serving as the lead clinical scientist on the clinical trial team. Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director. Other responsibilities include: Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data collection in alignment with the protocol in...
Professional Diversity Network Rahway, NJ, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Associate Director, Program Manager, Clinical Data Standards
Merck Job Description The Program Manager oversees the projects and or activities within Global Clinical Data Standards purview and the associated clinical information governance network in collaboration with the Director of Operations, Global Clinical Data Standards. They monitor, track, and control outcomes to resolve issues, conflicts, dependencies, and critical path deliverables using a consistent project management methodology. Through teamwork and a data driven approach, they would work analytically and creatively to solve problems. Coordinates our Company's standards governance network and facilitates our Company participating in and connecting with external standards related activities (e.g., CDISC, PhUSE, TransCelerate). Manages the definition, implementation, and maintenance of GCDS Standard Operating Procedures and supporting documentation to ensure compliance with worldwide regulatory and relevant internal requirements of our Company. Primary activities...
Professional Diversity Network Rahway, NJ, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Associate Director, Program Manager, Clinical Data Standards
Merck Job Description The Program Manager oversees the projects and or activities within Global Clinical Data Standards purview and the associated clinical information governance network in collaboration with the Director of Operations, Global Clinical Data Standards. They monitor, track, and control outcomes to resolve issues, conflicts, dependencies, and critical path deliverables using a consistent project management methodology. Through teamwork and a data driven approach, they would work analytically and creatively to solve problems. Coordinates our Company's standards governance network and facilitates our Company participating in and connecting with external standards related activities (e.g., CDISC, PhUSE, TransCelerate). Manages the definition, implementation, and maintenance of GCDS Standard Operating Procedures and supporting documentation to ensure compliance with worldwide regulatory and relevant internal requirements of our Company. Primary activities...
Professional Diversity Network Rahway, NJ, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Associate Director, Program Manager, Clinical Data Standards
Merck Job Description The Program Manager oversees the projects and or activities within Global Clinical Data Standards purview and the associated clinical information governance network in collaboration with the Director of Operations, Global Clinical Data Standards. They monitor, track, and control outcomes to resolve issues, conflicts, dependencies, and critical path deliverables using a consistent project management methodology. Through teamwork and a data driven approach, they would work analytically and creatively to solve problems. Coordinates our Company's standards governance network and facilitates our Company participating in and connecting with external standards related activities (e.g., CDISC, PhUSE, TransCelerate). Manages the definition, implementation, and maintenance of GCDS Standard Operating Procedures and supporting documentation to ensure compliance with worldwide regulatory and relevant internal requirements of our Company. Primary activities...
Professional Diversity Network North Wales, PA, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Associate Director, Program Manager, Clinical Data Standards
Merck Job Description The Program Manager oversees the projects and or activities within Global Clinical Data Standards purview and the associated clinical information governance network in collaboration with the Director of Operations, Global Clinical Data Standards. They monitor, track, and control outcomes to resolve issues, conflicts, dependencies, and critical path deliverables using a consistent project management methodology. Through teamwork and a data driven approach, they would work analytically and creatively to solve problems. Coordinates our Company's standards governance network and facilitates our Company participating in and connecting with external standards related activities (e.g., CDISC, PhUSE, TransCelerate). Manages the definition, implementation, and maintenance of GCDS Standard Operating Procedures and supporting documentation to ensure compliance with worldwide regulatory and relevant internal requirements of our Company. Primary activities...
Professional Diversity Network North Wales, PA, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Study Manager, Clinical Research Operations - Ophthalmology - Hybrid
Merck Job Description Job Summary This position contributes to the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to develop your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities May have specific operational responsibilities for asingle study or across multiple studies (e.g., operational deliverables, clinical & ancillary supplies planning/tracking, lab specimen tracking, status update reports, study closeout activities). May be responsible for tracking study timelines using project management tools. Shares technical expertise with team members. May interact with internal and external stakeholders (e.g.,study team, vendors, committees) in support of clinical trial objectives. Core Skills Working knowledge of clinical...
Professional Diversity Network Rahway, NJ, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Senior Scientist, Clinical Research Operations - Ophthalmology
Merck Job Description This position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership, technical skills, and scientific acumen as part of a global, cross-functional team. Job Responsibilities Responsible for leading specific aspects of clinical/scientific execution of clinical protocol(s). This may include: Serving as the lead clinical scientist on the clinical trial team. Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director. Other responsibilities include: Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data collection in alignment with the protocol in...
Professional Diversity Network Philadelphia, PA, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Study Manager, Clinical Research Operations - Ophthalmology - Hybrid
Merck Job Description Job Summary This position contributes to the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to develop your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities May have specific operational responsibilities for asingle study or across multiple studies (e.g., operational deliverables, clinical & ancillary supplies planning/tracking, lab specimen tracking, status update reports, study closeout activities). May be responsible for tracking study timelines using project management tools. Shares technical expertise with team members. May interact with internal and external stakeholders (e.g.,study team, vendors, committees) in support of clinical trial objectives. Core Skills Working knowledge of clinical...
Professional Diversity Network North Wales, PA, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Study Manager, Clinical Research Operations - Ophthalmology - Hybrid
Merck Job Description Job Summary This position contributes to the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to develop your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities May have specific operational responsibilities for asingle study or across multiple studies (e.g., operational deliverables, clinical & ancillary supplies planning/tracking, lab specimen tracking, status update reports, study closeout activities). May be responsible for tracking study timelines using project management tools. Shares technical expertise with team members. May interact with internal and external stakeholders (e.g.,study team, vendors, committees) in support of clinical trial objectives. Core Skills Working knowledge of clinical...
Professional Diversity Network Philadelphia, PA, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Senior Scientist, Clinical Research Operations - Ophthalmology
Merck Job Description This position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership, technical skills, and scientific acumen as part of a global, cross-functional team. Job Responsibilities Responsible for leading specific aspects of clinical/scientific execution of clinical protocol(s). This may include: Serving as the lead clinical scientist on the clinical trial team. Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director. Other responsibilities include: Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data collection in alignment with the protocol in...
Professional Diversity Network North Wales, PA, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Senior Scientist, Clinical Research Operations - Ophthalmology
Merck Job Description This position leads the scientific planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership, technical skills, and scientific acumen as part of a global, cross-functional team. Job Responsibilities Responsible for leading specific aspects of clinical/scientific execution of clinical protocol(s). This may include: Serving as the lead clinical scientist on the clinical trial team. Leading medical monitoring team in review and interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director. Other responsibilities include: Collaborating cross-functionally in the development of Protocol and related study materials (e.g., ICF documents / amendments); Partners with the Study Manager on study deliverables. Ensuring CRF design supports data collection in alignment with the protocol in...
Professional Diversity Network Rahway, NJ, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Study Manager, Clinical Research Operations - Ophthalmology - Hybrid
Merck Job Description Job Summary This position contributes to the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to develop your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities May have specific operational responsibilities for asingle study or across multiple studies (e.g., operational deliverables, clinical & ancillary supplies planning/tracking, lab specimen tracking, status update reports, study closeout activities). May be responsible for tracking study timelines using project management tools. Shares technical expertise with team members. May interact with internal and external stakeholders (e.g.,study team, vendors, committees) in support of clinical trial objectives. Core Skills Working knowledge of clinical...
Professional Diversity Network North Wales, PA, USA Full-Time
Professional Diversity Network
Mar 25, 2026  
Study Manager, Clinical Research Operations - Ophthalmology - Hybrid
Merck Job Description Job Summary This position contributes to the operational planning and execution of one or more clinical trials. In this position, you will have the opportunity to develop your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities May have specific operational responsibilities for asingle study or across multiple studies (e.g., operational deliverables, clinical & ancillary supplies planning/tracking, lab specimen tracking, status update reports, study closeout activities). May be responsible for tracking study timelines using project management tools. Shares technical expertise with team members. May interact with internal and external stakeholders (e.g.,study team, vendors, committees) in support of clinical trial objectives. Core Skills Working knowledge of clinical...
Professional Diversity Network Rahway, NJ, USA Full-Time
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