18 research development intern jobs found in Rahway

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...

Merck Job Description The Associate Director leads strategic communications to position our company as a trusted partner in advancing global health equity and enabling sustainable access to our medicines and vaccines. By unifying enterprisewide storytelling, the role drives a global communications strategy that elevates our company commitments to expanding patient access and strengthening health systems across both commercial and noncommercial initiatives. Key Responsibilities Deliver internal and external communications supporting major enterprise initiatives including the Impact Report, philanthropic programs, quarterly results and high-visibility events (e.g. BIO, UNGA, WHA). Contribute to a multiyear global health equity communications strategy aligned with our company commercial, therapeutic area and sustainable access goals. Partner with teams across our company value chain - including Corporate Affairs, Research, Manufacturing, country managers and...

Merck Job Description Associate Principal Scientist, Outcomes Research Under the guidance of a senior leader, the Associate Principal Scientist (Associate Director), Outcomes Research - Head & Neck Cancer will be a member of the overall team responsible for evidence strategy and planning. Will develop and maintain tumor and indication expertise relevant to the asset. Will assess unmet medical need and value across tumors/indications for the asset for asset-level tumor/indication prioritization discussions. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient-reported outcomes assessments, and systematic reviews and meta-analyses. Incumbent is expected to contribute to product development and marketing strategies throughout the lifecycle to ensure that product...

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...

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...

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...

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...

Merck Job Description Summary This position contributes to the scientific planning and execution of one or more clinical trials. Assists the Lead Clinical Scientist and study team with the scientific conduct of clinical studies. In this position, you will have the opportunity to develop your leadership, technical skills, and scientific acumen as part of a global, cross-functional team. Job Responsibilities Responsible for specific clinical/scientific activities on a single study or across multiple studies (e.g., medical monitoring, lab specimen tracking/reconciliation, adjudication support, preparation of meeting materials). Support development of Protocol and related study materials (e.g., ICF documents/amendments, data management deliverables). May interact with internal and external stakeholders (e.g., country operations, committees, vendors) in support of clinical study objectives. Support development of site and CRA training materials Prepare...

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...

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...

Merck Job Description Associate Principal Scientist, Outcomes Research Under the guidance of a senior leader, the Associate Principal Scientist (Associate Director), Outcomes Research - Head & Neck Cancer will be a member of the overall team responsible for evidence strategy and planning. Will develop and maintain tumor and indication expertise relevant to the asset. Will assess unmet medical need and value across tumors/indications for the asset for asset-level tumor/indication prioritization discussions. Types of studies executed include prospective and retrospective observational studies to characterize disease burden and epidemiology, treatment patterns, healthcare resource utilization and costs, physician and patient satisfaction surveys, clinical and patient-reported outcomes assessments, and systematic reviews and meta-analyses. Incumbent is expected to contribute to product development and marketing strategies throughout the lifecycle to ensure that product...

Merck Job Description The Associate Director leads strategic communications to position our company as a trusted partner in advancing global health equity and enabling sustainable access to our medicines and vaccines. By unifying enterprisewide storytelling, the role drives a global communications strategy that elevates our company commitments to expanding patient access and strengthening health systems across both commercial and noncommercial initiatives. Key Responsibilities Deliver internal and external communications supporting major enterprise initiatives including the Impact Report, philanthropic programs, quarterly results and high-visibility events (e.g. BIO, UNGA, WHA). Contribute to a multiyear global health equity communications strategy aligned with our company commercial, therapeutic area and sustainable access goals. Partner with teams across our company value chain - including Corporate Affairs, Research, Manufacturing, country managers and...

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...

Merck Job Description Summary This position contributes to the scientific planning and execution of one or more clinical trials. Assists the Lead Clinical Scientist and study team with the scientific conduct of clinical studies. In this position, you will have the opportunity to develop your leadership, technical skills, and scientific acumen as part of a global, cross-functional team. Job Responsibilities Responsible for specific clinical/scientific activities on a single study or across multiple studies (e.g., medical monitoring, lab specimen tracking/reconciliation, adjudication support, preparation of meeting materials). Support development of Protocol and related study materials (e.g., ICF documents/amendments, data management deliverables). May interact with internal and external stakeholders (e.g., country operations, committees, vendors) in support of clinical study objectives. Support development of site and CRA training materials Prepare...

Merck Job Description Our Engineers support internal and external manufacturing operations to ensure our facilities remain operational, continuously improve and innovate. With our extensive range of facilities and environments, our Engineers have opportunities across many diverse areas including Biological, Chemical, Automation, Capital Projects, Maintenance, Safety, Process Development, Technical Services, Utilities and Validation. Director Global Engineering Solutions Projects is responsible for leading the Delivery of a large Capital Program (~$1B).Guide the team to carefully plan, identify risks and mitigation strategies, track and monitor progress, escalate risks and cascade information. Align a cross-functional team around the project mission/work plan. Interface and align with key Service Providers of Engineering, Procurement, Equipment, Construction Management and Commissioning/Qualification services. Initial assignment is as described above, but future roles and...

Merck Job Description The Analytical Research and Development group has an opening for a Senior Specialist based in Rahway, NJ. Join us and experience our culture first-hand - one of strong ethics & integrity, diversified experiences, exceptional science, and a resounding passion for improving human health through innovative drug delivery technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate with talented and dedicated colleagues while developing and expanding your career. In your role as Senior Specialist, you will be part of a cross-functional team in charge of testing, managing, coordinating, and facilitating analytical support to enable medical device and combination product development and commercialization. We are seeking a hands-on, lab-based specialist to support GMP testing of devices (components, sub-assemblies, and full devices) and combination products (drug-delivery products) including...

Merck Job Description Role Summary The Global Medical Affairs and Strategic Alliances Director position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. This position is accountable for supporting Medical Affairs (MA) activities for external strategic alliances and partnerships. The Global Medical Affairs and Strategic Alliances Director coordinates and supervises all alliance MA activities and collaborates with internal and external partners as they relate to these global activities. The Director supports the alignment of our scientific and medical strategies across the portfolio of relevant company products. The Director works on the continuous development and improvement of cross-functional alignment, systems and processes impacting Medical Affairs to ensure that work is uniform, complete, and consistent with relevant collaboration agreement. The Global Medical...

PerkinElmer Responsibilities Location Rahway, New JerseyUS Job ID REQ-056801 The OneSource Site Leader is responsible for the oversight, and performance management of the OneSource Laboratory Support Coordinator and Service Engineer team supporting a strategic customer account. This role partners closely with the OneSource Service Area Manager to ensure standardized, high-quality service delivery and consistent customer responsiveness across the supported sites. The OneSource Site Leader works in close collaboration with the customer stakeholders, and internal leadership to ensure laboratory support services, including Service Engineering, Lab Support Coordinator and EHS services are executed in compliance with regulatory, safety, and contractual requirements. The role is accountable for tracking, analyzing, and reporting critical KPIs while driving continuous improvement, operational efficiency, and customer satisfaction. Job Responsibilities OneSource...