Lead Clinical Trial Operations Manager Jobs in Florham Park, NJ

Purpose:Leads the direction planning and interpretation of clinical trials or research activities of one or more clinical development programs. Participates in and may lead cross-functional teams to generate deliver and disseminate high-quality clinical data supporting overall product scientific and...

The Medical Affairs organization provides patients healthcare providers and payers everywhere with the practical and clinically relevant information and solutions they need to use AbbVie products safely and effectively throughout the product lifecycle and the patients journey.The Scientific Director...

The Associate Director Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional multidisciplinary therapeutic teams and executes multidivisional initiatives. The Associate Director envisions the future by using global marketplace technology and...

OverviewThe role will support the Global Medical Affairs Lead for virology and rare disease assets with flexibility to expand as the portfolio evolves. ResponsibilitiesProvide strategic advisory input to internal Medical Affairs leadership on scientific positioning for assigned assetsDevelop draft s...

OverviewThe Senior Medical Director Global Medical Affairs (Virology and Rare Diseases) provides global medical/scientific leadership for assigned assets serving as a subject matter expert and strategic partner across cross-functional teams. This is a global individual contributor role with asset-le...

OverviewThe Senior Medical Director Global Medical Affairs (Virology and Rare Diseases) provides global medical/scientific leadership for assigned assets serving as a subject matter expert and strategic partner across cross-functional teams. This is a global individual contributor role with asset-le...

ResponsibilitiesManages the design and implementation of one or more clinical development programs in support of an overall Product Development Plan based on strong medical and scientific principles knowledge of compliance and regulatory requirements AbbVies customers markets business operations and...

OverviewThe Senior Medical Director Medical Affairs (Virology and Rare Diseases) provides global medical/scientific leadership for assigned assets serving as a subject matter expert and strategic partner across cross-functional teams. This is a global individual contributor role with asset-level acc...

OverviewThe Associate Director GCP/GVP Quality Assurance provides senior-level quality oversight for Shionogis clinical development and pharmacovigilance activities ensuring compliance with ICH FDA EMA PMDA MHRA and other global regulatory requirements. Serving as the QA representative to assigned s...

The Director Medical Affairs  Health Impact (MHI) is a key scientific expert within the Pipeline Psychiatry Therapeutic Area.  The position supports the development and execution of the Pipeline Psychiatry medical strategy by leading execution of strategic insight and educational initiatives in psyc...

OverviewThe Senior Director Field Medical Affairs (FMA) in COVID-19/Virology will be responsible for providing leadership oversight and overall direction to a group of US Medical Science Liaisons (MSLs). Will oversee and manage the MSL Team in cultivating Key Opinion Leaders (KOLs) and emerging thou...

OverviewThe Senior Director Field Medical Affairs (FMA) in COVID-19/Virology will be responsible for providing leadership oversight and overall direction to a group of US Medical Science Liaisons (MSLs). Will oversee and manage the MSL Team in cultivating Key Opinion Leaders (KOLs) and emerging thou...

OverviewThe Director Field Medical Affairs (FMA) in COVID-19/Virology is responsible for leading and managing a regional team of Medical Science Liaisons (MSLs) driving scientific engagement and supporting the tactical execution of medical affairs strategies for COVID-19/Virology. This role ensures...

With supervision oversees the direction planning execution and interpretation of clinical trials or research activities of a clinical development program. Participates in cross-functional teams to generate deliver and interpret high-quality clinical data supporting overall product scientific and bus...

The Associate Director Regulatory Affairs Chemistry Manufacturing and Controls (CMC) works with internal and external partners to deliver products to patients. This role offers the opportunity to apply and further develop regulatory and technical expertise in small molecule CMC development of peptid...

The Senior Research Statistician Statistics is responsible for providing statistical support to the research and development organization. Specific areas of work may include clinical trials patient safety and global medical affairs (GMA). The Senior Research Statistician works in partnership with ex...

OverviewThe Compliance Field Liaison will serve as a key point of contact between Compliance and field-based personnel in Commercial functions (Sales Managed Markets) and Medical functions (MSLs) in support of the commercialization and communication of promotional and medical information regarding p...