15412 massage therapist jobs found

Investigate Cell Therapy - Immuno-Oncology Combinations: Harnessing novel in vitro and in vivo models in conjunction with clinical translatability to evaluate Mechanism of Action (MoA) of drug combinations in cell therapy The exciting Postdoctoral Program at AbbVie is designed for experimental research that attains optimal solutions for patients. Participants in the program receive a balance of structured learning and work experience, while being mentored by renowned industry leaders intent on delivering cutting-edge advancements in Discovery and Development Sciences. Postdoctoral positions last 2-3 years and provide the resources and opportunities not just to publish in per-reviewed journals, but also to collaborate with various teams across the organization, from Antibody Engineering to Drug Metabolism and Pharmacokinetics for ascertaining therapeutic index. Successful individuals are poised to successfully compete for internal scientific roles within the organization....

About AbbVie AbbVie (NYSE:ABBV) is a global, research-driven biopharmaceutical company committed to developing innovative advanced therapies for some of the world’s most complex and critical conditions. The company’s mission is to use its expertise, dedicated people, and unique approach to innovation to markedly improve treatments across four primary therapeutic areas: immunology, oncology, virology and neuroscience. In more than 75 countries, AbbVie employees are working every day to advance health solutions for people around the world. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook or LinkedIn. Reporting to the Director, Global Brand Team Lead, Oncology, MM this position supports the development and execution of the marketing strategies and tactics at the Global, Areas, and Country-Affiliate level. Collaborates and engages with a matrixed team, which includes (but not limited to): market access, medical affairs,...

Want to join an award-winning team? We OFFER that. Ready to make a Worldwide impact? We OFFER that too. Want to have a thriving career? We OFFER that. Ready to drive innovation? We OFFER that too. At AbbVie, we offer you the resources and a global reach to empower your innovative mindset. From day one, we’ve known it takes teamwork and collaboration to develop the scientific breakthroughs, innovative pipelines, and therapies that change millions of patients’ lives around the world. In short, we know it takes “you” to make those ground-breaking advancements happen. We take pride in serving and supporting our communities and protecting the environment, making a lasting impact that's felt within healthcare and beyond. We are always searching for talented Supply Chain professionals to join our diverse organization, which provides supply chain support/direction to multiple functional areas across AbbVie . So, let’s tell you a little more about the potential roles......

Welcome to AbbVie! At AbbVie, we offer the resources and a global reach to empower your innovative mindset. From day one, we've know it takes teamwork and collaboration to develop the scientific breakthroughs, innovative pipelines, and therapies that change millions of patients' lives around the world. In short, we know it takes "you" to make those ground breaking advancements happen. We take pride in serving and supporting our communities and protecting the environment, making a last impact thats felt within healthcare and beyond. We are now recruiting a Account Manager, Third Party Manufacturing to join our diverse external and contract manufacturing team in Massachusetts. As part of this diverse and inclusive team, you will... Serve as primary contact between AbbVie and Third Party Customer or Third Party Manufacturer. Must travel to TPM/TPC sites and establish meaningful working relationships and understanding of the TPM's capabilities and/or Customer needs. Primary AbbVie...

Job DescriptionThe Senior Medical Director, Global Medical Safety, oversees the benefit-risk strategy for a portfolio of marketed and clinical development products. The individual must demonstrate agility, the ability to prioritize, and the capability to provide strategic leadership across multiple disease areas and modalities. Must be comfortable working in an entrepreneurial environment to advance compounds' safety and biological understanding through the life cycle. The individual who assumes this position will interact with multiple levels of management within Biogen, external stakeholders in the medical community, and global regulatory authorities and is expected to influence the strategic direction of complex issues for the assigned therapeutic areas.This individual will also be accountable for performing and overseeing business development evaluations and recommendations from Global Medical Safety. Finally, the individual will be responsible for continuous process...

Company DescriptionAt Biogen, we offer a workplace that is unique, connected, resilient and impactful. Our purpose to find cures for rare diseases is auniquefocus within our industry. We areconnectedas a team by this shared purpose, the pride we have inour work,andthe inspiration we obtainfromthe liveswe'rechanging.We areresilientas we overcome obstacles, following the scienceto deliverfor our patients.Most of all, our workallows us tohaveanimpact. An impacton our patients' livesandon changing the course of medicine.Job DescriptionAbout this role As the Senior Principal Biostatistician, you are responsible for leading study design and data analysis and providing the statistical expertise for company products within one or more therapeutic areas in clinical development, biomarker development, research, Biotherapeutic and Medicinal Sciences (BTMS) or Pharmaceutical Operations & Technology (PO&T). You act as independent Study Management Team (SMT) or Research and Development...

Company DescriptionAt Biogen, we offer a workplace that is unique, connected, resilient and impactful. Our purpose to find cures for rare diseases is auniquefocus within our industry. We areconnectedas a team by this shared purpose, the pride we have inour work,andthe inspiration we obtainfromthe liveswe'rechanging.We areresilientas we overcome obstacles, following the scienceto deliverfor our patients.Most of all, our workallows us tohaveanimpact. An impacton our patients' livesandon changing the course of medicine.Job DescriptionAbout this roleAs the Associate Director of Biostatistics, you are responsible for leading complex or integrated study design and data analysis in clinical development, biomarker development, research, Biotherapeutic and Medicinal Sciences (BTMS) or Pharma Ops & Technology (PO&T). You act as Research and Development Project Team (RDPT) Biostatistician, to ensure valid and efficient study designs that allow clearly interpretable results, and timely...

Company DescriptionAt Biogen, we offer a workplace that is unique, connected, resilient and impactful. Our purpose to find cures for rare diseases is auniquefocus within our industry. We areconnectedas a team by this shared purpose, the pride we have inour work,andthe inspiration we obtainfromthe liveswe'rechanging.We areresilientas we overcome obstacles, following the scienceto deliverfor our patients.Most of all, our workallows us tohaveanimpact. An impacton our patients' livesandon changing the course of medicine.Job DescriptionAbout this roleAs the Associate Director of Biostatistics, you are responsible for leading complex or integrated study design and data analysis in clinical development, biomarker development, research, Biotherapeutic and Medicinal Sciences (BTMS) or Pharma Ops & Technology (PO&T). You act as Research and Development Project Team (RDPT) Biostatistician, to ensure valid and efficient study designs that allow clearly interpretable results, and timely...

Job DescriptionAs part of the IT Quality team, ensure the delivery of technically robust and compliant GxP computerized systems (CS) that withstand audits, both internal and external. The Sr. IT Quality Associate II is expected to have working-level knowledge of CS at the enterprise level, including the quality systems supporting the implementation and management of enterprise systems (i.e., change management, exceptions management, risk management). The Sr. IT Quality Associate II is expected to have foundational understanding of regulatory expectations for CS and be able to provide quality oversight and guidance to IT teams to support implementation of and management of enterprise computer systems. This role works with peers locally and globally, to ensure practices are consistent with requirements and expectations set forth within the governing QMS.WhatYou'llDoDrive the deployment of new GxP computerized systems through review and approval of life cycle deliverables in...

Job DescriptionAs part of the IT Quality team, ensure the delivery of technically robust and compliant GxP computerized systems (CS) that withstand audits, both internal and external. The Sr. IT Quality Associate II is expected to have working-level knowledge of CS at the enterprise level, including the quality systems supporting the implementation and management of enterprise systems (i.e., change management, exceptions management, risk management). The Sr. IT Quality Associate II is expected to have foundational understanding of regulatory expectations for CS and be able to provide quality oversight and guidance to IT teams to support implementation of and management of enterprise computer systems.This role works with peers locally and globally, to ensure practices are consistent with requirements and expectations set forth within the governing QMS.WhatYou'llDoDrive the deployment of new GxP computerized systems through review and approval of life cycle deliverables in compliance...

Job DescriptionThe Sr. Manager of Small Molecule Stability is responsible for contributing to key functional, tactical, and operational aspects of the Stability group at Biogen. Must have excellent written and verbal communication skills.This role Leads interactions with Quality, Regulatory Affairs, and Asset sub-teams to drive the establishment, assessment, and management of multiple stability programs.Reviews stability protocols, authors and reviews in-depth technically-sound stability reports in support of APRs,Annual Reports, expiry justifications and other reports as appropriate, and contributes to regulatory filings (IND/IMPD/BLA).Provides leadership for stability investigations and data interpretation and performs complex and sophisticated data analysis. Provides guidance and direction to direct reports.Monitors execution of stability studies for compliance to approved protocols and regulatory submissions.Manage all activities associated with managing global commercial and...

The Position Main Purpose of the Position: Participate in activities to enable Inspection Readiness, including facilitation of internal/external audits and managing activities to support US/exUS filings and regulatory inspections. This position will also include managing the process for identification and mitigation of site health authority compliance risks, management of emerging regulations (including drug product, medical device and combination product production) and systematic evaluation of new requirements, oversight for trending of Quality Compliance Performance, Supplier Management and acts as a Regulatory liaison. . Responsibilities: Develop and execute inspection/audit prep plans and manage the inspection readiness activities (maintain key contact list, prep/strategy sessions, inspection readiness training, etc.) Manage and maintain the Inspection Ready Room Conduct post-inspection lessons learned sessions Participate in cross site Inspection Readiness...

The Position Roche's Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development (Phase II - IIIA) clinical strategies and plans to deliver medically-differentiated therapies that provide meaningful improvement to patients. The PD Clinical Scientist participates in development of the Clinical Development (CD) strategy and plan and supports the assigned PD Medical Director/Clinical Development Physician(s) with various deliverables necessary for effective and efficient CD plan execution for the assigned molecule(s)/indication(s). PD Clinical Scientists have primary responsibilities for supporting PD Medical Directors/Clinical Development Physicians with clinical documentation, representing CD on various sub-teams or other appropriate forums, supporting training of study site personnel, acting as a primary point-of-contact for questions and inquiries to CD regarding CD studies or other programs, conducting...

The Position Roche's Clinical Development organization is structured by therapeutic area and is responsible for developing and executing the late development (Phase II - IIIA) clinical strategies and plans to deliver medically-differentiated therapies that provide meaningful improvement to patients. The PD Clinical Scientist participates in development of the Clinical Development (CD) strategy and plan and supports the assigned PD Medical Director/Clinical Development Physician(s) with various deliverables necessary for effective and efficient CD plan execution for the assigned molecule(s)/indication(s). PD Clinical Scientists have primary responsibilities for supporting PD Medical Directors/Clinical Development Physicians with clinical documentation, representing CD on various sub-teams or other appropriate forums, supporting training of study site personnel, acting as a primary point-of-contact for questions and inquiries to CD regarding CD studies or other programs, conducting...

The Position At Roche, 94,000 people across 100 countries are pushing back the frontiers of healthcare. Working together, we've become one of the world's leading research-focused healthcare groups. Our success is built on innovation, curiosity, and diversity. We believe every employee makes a difference. We are passionate about transforming patients' lives. We are courageous in both decision and action, we believe that good business means a better world. This position is part of the Pharma Technical Cell and Individualized Medicines Team responsible for the process development, manufacture and supply of personalized immunotherapies in collaboration with our global partners. Job Summary: Orchestration and Exception Management (O&EM) is a new and fundamental capability for Pharma Technical Operations (PT) in order to deliver a future portfolio of Cell & Gene Therapy (CGT) products. This portfolio of new products comes with the great promise to bring unprecedented...

*This is a temporary assignment. The individual in this role will be employed by a third party, not by Genentech Target Hire: March 1st Device and Packaging Development designs, develops, scales, transfers, and supports manufacturing of combination product drug delivery devices for Genentech (Roche) to enable safe, effective, and convenient administering therapies. Examples of combination products include prefilled syringes, pen injectors, auto-injectors, inhalers, transdermal pumps and patches, and kits containing drug administration devices or components. Device and Packaging Development's project management office connects people, processes, and systems to enable compliant and agile team execution and deliver novel technologies & medicines to patients by delivering high-value project management core competencies to achieve results. The project manager is an integral part of a multifunctional project team, including device engineering, pharmaceutical development,...

The Position Provides biomarker operational expertise and guidance to multiple cross-functional global Protocol Execution Teams (PETs), to implement scientifically driven clinical development plans. Single point of contact on Biomarker Sub Team (BMST), Companion Diagnostic Joint Project team (CDx JPT), Clinical Sub Team (CST), PET and with CRO partners on all aspects of biomarker operations Ensures the timely and efficient delivery of all biomarker operational aspects of gRED clinical studies, including company collaboration and academic collaboration studies across all stages (start-up, conduct and close-out), in accordance with the appropriate quality standards including ICH/GCP and applicable regulations. Main Responsibilities and Accountabilities: Provides biomarker operational expertise and guidance to global Protocol Execution Teams (PETs) Accountable for executing exploratory and companion diagnostic biomarker strategy, including planning, coordinating, and...

The Position This individual also lives the CMG Operating Principles ( I put the patient first always; I am tenacious in meeting customer needs; I act on behalf of the whole company, not just my own team; I am accountable; I use time and resources to create the most impact; I am inclusive; I have a bias for action; I build a culture of trust; My career will thrive as I grow my capabilities and increase my impact; I act with integrity ) Core Competencies The successful candidate will demonstrate the following competencies critical to this role : Communication & influencing: Ability to frame information accurately and concisely, appropriately tailoring communications to varying audiences, both internal and external. Ability to distill complex topics, issues, and analytical components; ability to communicate these topics to others with varying backgrounds and expertise. Ability to effectively influence others without authority Teamwork & Collaboration: A drive to...

The Position Development Sciences Informatics is seeking a talented and experienced Informatician to lead informatics efforts supporting a wide variety of drug development disciplines. Development Sciences (DevSci) is a translational science organization that plays a critical role in Genentech Research and Early Development as well as late stage development of our products at Roche. DevSci supports drug discovery and development projects across all therapeutic areas from discovery to launch and beyond. We are poised at a unique time when large volumes of complex and varied internal and external data needs to be readily accessible to ensure that swift interpretation and decision making can occur. These data impact decisions in ongoing preclinical and clinical programs, and provide key knowledge to inform new target discovery. DevSci Informatics is accountable for leading the strategy and execution around data lifecycle management, data standards, analytics infrastructure, ongoing...

Janssen Research & Development, L.L.C., a division of Johnson & Johnson's Family of Companies is recruiting for an Associate Scientist to join a growing team focused on cell therapy process development for the development of innovative treatments for cancer. The position is a key part of the growing API Cell and Gene Therapy Organization located in Spring House, PA site. At the Janssen Pharmaceutical Companies of Johnson & Johnson, what matters most is helping people live full and healthy lives. We focus on treating, curing and preventing some of the most devastating and complex diseases of our time. And we pursue the most promising science, wherever it might be found. We are Janssen. Our mission drives us. Our patients inspire us. We collaborate with the world for the health of everyone in it. Janssen Research & Development, LLC discovers and develops innovative medical solutions to address important unmet medical needs in oncology, immunology, neuroscience,...