Berklee College of Music Job Description: Reporting to the Sr. Human Resources Business Partner, the HR Generalist collaborates with HR colleagues to execute HR initiatives, programs and services that support Berklee's strategic goals. The HR Generalist works closely with the HR Partners, talent acquisition, compensation, and benefits teams to provide services in the areas of recruiting, general employee relations, organizational/professional development, compensation, and policy interpretation. The HR Generalist will also play an integral role in compliance and risk mitigation efforts within the department. This includes creating processes and systems to ensure full adherence to federal regulations related to I-9, CORI, FLSA, etc. In collaboration with Sr. HR Partners, responsible for delivering programs and services that address general employee relations, organizational/professional development and employee engagement to assigned areas. Serve as first point of contact for...

Site Name: USA - Massachusetts - Waltham Posted Date: Sep 13 2024 We are seeking an Associate Director level, Quantitative Systems Pharmacology Lead for our Clinical Pharmacology Modelling and Simulation (CPMS) department. Quantitative Systems Pharmacology (QSP) is a discipline that uses mechanistic mathematical models and disease platforms to enhance the robustness and quality of decision-making from exploratory research through clinical development. We are seeking a highly motivated individual to develop and apply QSP models to guide clinical study designs and mechanistic interpretation of study results in support of development of treatments and combination of treatments for a variety of diseases and therapeutic areas. The successful candidate will be responsible for integrating and sharing data and knowledge in a highly stimulating, collaborative, and multi-disciplinary environment to influence clinical study decisions and develop a deeper understanding of physiological...

SS&C SS&C is a global provider of investment and financial services and software for the financial services and healthcare industries. Named to Fortune 1000 list as top U.S. company based on revenue, SS&C is headquartered in Windsor, Connecticut and has 20,000+ employees in over 90 offices in 35 countries. Some 18,000 financial services and healthcare organizations, from the world's largest institutions to local firms, manage and account for their investments using SS&C's products and services. Job Description About SS&C Technologies SS&C is a global provider of investment, financial services and software for the financial services and healthcare industries. Named to Fortune 1000 list as top U.S. company based on revenue, SS&C is headquartered in Windsor, Connecticut and has 20,000+ employees in over 90 offices in 35 countries. Some 18,000 financial services and healthcare organizations, from the world's largest institutions to local firms,...

Walgreens Job Description Our pharmacy technician positions have undergone an exciting transformation, moving from a transaction-based environment to a much more patient-centric one. As a Walgreens Pharmacy Technician or Pharmacy Technician Apprentice, you'll be front and center - interacting with our customers and developing strong patient relationships. Pharmacy is the core of our business, and our pharmacy technicians enjoy all the tools and support - including the latest technology - to grow their careers and reach their goals. Walgreens is proud to invest & champion an "earn while you learn" Pharmacy Technician Training Program recognized by ASHP & Department of Labor. This apprenticeship program gives you an entry point to a career in health care by guiding you in taking steps towards becoming a Pharmacy Technician Certification Board (PTCB) Certified Pharmacy Technician and helping you maintain the high level of skill required in the pharmacy care industry....

Site Name: USA - Pennsylvania - Upper Providence, Belgium, UK - Hertfordshire - Stevenage, UK - London, UK - London - New Oxford Street, USA - Massachusetts - Cambridge, USA - Massachusetts - Waltham, USA - North Carolina - Durham, USA - Pennsylvania - Philadelphia Posted Date: Sep 12 2024 Are you looking for a role where you will serve as a key strategic partner representing Global Regulatory activities? If so, this Director of Regulatory Affairs, CMC could be an exciting opportunity to explore. This role will provide strategic direction and guidance on both global project and key strategic business initiatives. Within Global Regulatory Affairs, our Chemistry, Manufacturing and Controls (CMC) organization provides regulatory leadership to CMC development teams and the Pharma Supply Chain organization to enable approval of new medicines and uninterrupted supply of our medicines to patients. Our work spans all formulation types, novel technologies, and multiple modalities for...

Site Name: UK - Hertfordshire - Stevenage, USA - Massachusetts - Waltham Posted Date: Sep 10 2024 Although this role is advertised in GSK HQ and Waltham, candidates based in other locations may be considered on a case by case basis. At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people over the next 10 years. R&D is committed to discovering and delivering transformational vaccines and medicines to prevent and change the course of disease. Science and technology are coming together in a way they never have before, and we have strong tech-enabled capabilities that allow us to build a deeper understanding of the patient, human biology and disease mechanisms, and transform medical discovery. We are revolutionising the way we do R&D. We’re uniting science, technology and talent to get ahead of disease together. Find out more: Our approach to R&D . The Department of Clinical Pharmacology Modelling and...

Site Name: USA - Pennsylvania - Upper Providence, USA - Massachusetts - Waltham Posted Date: Jul 1 2024 Are you looking to expand your expertise with scientific technology in a global environment that allows you to keep pace with the speed of change? At GSK, we are transforming how new scientific technologies are used to improve patient’s lives. Job Description: The Senior Manager , Chemical Development will be responsible for the development, optimization, implementation, and management of robust, cost effective, and safe processes for the manufacture of small molecules including Oligonucleotide Active Pharmaceutical Ingredients (APIs) and Antibody Drug Conjugates (ADCs). The incumbent will be responsible for the technical development, support, validation and commercialization of drug substances using an external and internal network of providers. This position is integral to the advancement of GSK's growing portfolio of drug candidates and technology programs. The...

Site Name: USA - Pennsylvania - Philadelphia, Durham Blackwell Street, Home Worker - USA, Philadelphia Walnut Street, Waltham Posted Date: Jul 12 2024 Job Purpose The US Medical Affairs Leader is the single point of medical accountability for a medicine or medicine(s) and leads the development and execution of US Medical Affairs strategy and plans. This role is critical to the overall success of the medicine and in ensuring patients benefit from our scientific advancements. This leader is responsible for ensuring strategic alignment with US Commercial, Global Medical, and the overall US Medical matrix. Position will lead, directly and indirectly, a Medical Matrix Team (MMT) responsible for developing and executing US Medical Affairs Strategic and tactical plans. Key responsibilities Accountable for developing US medical strategy, ensuring medical strategy and plans are aligned with commercial asset strategy where appropriate; Co-Leads the US Integrated Brand...

Site Name: USA - Pennsylvania - Upper Providence, USA - Maryland - Rockville, USA - Massachusetts - Waltham, USA - Pennsylvania - Philadelphia Posted Date: Jul 2 2024 Accountable to GRL and Global Regulatory TA Head for development of appropriate regional regulatory strategy(s) and for delivery according to plans. In conducting role, planning will be on a multiple year horizon, with delivery requiring extensive matrix working within GSK to VP level and representing GSK with at least the local regulatory agency. Work with the Early/Medicine Development Team (EDT/MDT) or GRL, to ensure a robust regulatory strategy is in place to support the development program to meet the needs of the key markets identified in the Integrated Asset plan and the Medicine Profile. Work closely with local / regional commercial team to secure best possible labelling commensurate with the available data. Lead interactions with local / regional regulatory authorities. Key Responsibilities:...

Site Name: USA - Massachusetts - Waltham, UK - Hertfordshire - Stevenage, USA - Pennsylvania - Upper Providence Posted Date: Jul 17 2024 The Associate Director of Analytical Development will lead a team of analytical scientists responsible for development, manufacturing, release and stability testing, and characterization of drug substances/API and drug products of Small Molecule and Oligonucleotide therapeutic modalities within the Strategic External Development (SED) organization. The Associate Director will be responsible for people and project management, who would also function as an analytical project lead and technical lead in a broad analytical development role that spans from managing collaboration with appointed CDMOs to overseeing, developing, and executing aligned GSK and CDMO goals for development of small molecules and oligonucleotides. It will further extend to investigation, preparation and reviewing of CMC content for regulatory submissions, as well as...

Site Name: USA - Pennsylvania - Upper Providence, UK - Hertfordshire - Stevenage, USA - Massachusetts - Waltham Posted Date: Jul 25 2024 Do you have experience in small molecule Drug Development and an interest in Biotransformation and Drug-Drug Interaction assessment? Are you interested in expanding your role? The GSK global DMPK organization is looking for a DMPK Project Specialist (Associate Director) to join the Development DMPK Project Specialist group, based in either Philadelphia, USA, Stevenage, UK, or Boston, USA. The candidate must have an in-depth knowledge of small molecule drug development and a keen interest in understanding biotransformation and drug disposition. In addition, the candidate should have experience in the authoring of regulatory documentation (e.g. Investigator Brochures, briefing documents for regulatory agency meetings and responses to regulatory queries. Working collaboratively with key matrix project team members (i.e. Project Leaders,...

Site Name: USA - Massachusetts - Cambridge, USA - Massachusetts - Waltham, USA - North Carolina - Durham, USA - Pennsylvania - Upper Providence Posted Date: Jul 22 2024 As a Director of Business Development, Technology , you will be a leader within the Business Development team, responsible for strengthening our research and development pipeline through external innovation encompassing all stages of science and drug development. This role involves working on end-to-end transactions, that support GSK’s technology ambition, spanning licensing, divestments to whole company acquisitions. GSK’s overall Research & Development (R&D) strategy focuses on science related to the immune system, the use of human genetics and advanced technologies. These unlock the potential of new areas of science, including AI/ML and mRNA-based therapeutics, enabling us to design and develop new classes of medicine and bring them to patients more quickly and cost-effectively. The technology...

Site Name: USA - Massachusetts - Waltham, GSK HQ, Stevenage, USA - North Carolina - Durham, USA - Pennsylvania - Upper Providence Posted Date: Sep 6 2024 We have an exciting opportunity at GSK for a highly motivated and experienced director-level quantitative clinical pharmacologist to join our team supporting the oncology therapeutic area as part of the global Clinical Pharmacology Modelling and Simulation (CPMS) department. If you are energized by leveraging your clinical pharmacology and pharmacometrics experience to accelerate the development of oncology therapeutics this role may be for you. Job Purpose As a Director of Clinical Pharmacology Modelling and Simulation (CPMS) you will be part of a large science driven team delivering clinical pharmacology and modelling & simulation excellence to research and development programs. You’ll have the opportunity to work on a wide diversity of therapeutic modalities including small molecules, biologics, and...

CSL Behring The Opportunity: The TA Lead has significant responsibility and impact. The position will be instrumental in forming strategic partnerships with the respective business leads/TA leads. The TA Lead will lead and oversee the global management of intellectual property matters as well as provide strategic guidance to advance the TA IP assets and creating commercial business value and commercial security and confidence. This role is integral to developing, defending and enforcing the organization's global TA patent portfolio, developing and enforcing the global TA's Regulatory exclusivities' portfolio, as well as ensuring compliance with intellectual property laws, thereby supporting the company's broader business objectives. You will lead and support all IP aspects of deals planned and executed by the TA's. You will partner with the TA lead and associates on developing life cycle management and life cycle initiatives which involve IP amongst other things. The...

Site Name: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Durham Blackwell Street, USA - Massachusetts - Waltham Posted Date: Sep 4 2024 Would you like to be part of GSK’s Vaccine Epidemiology team, with an opportunity to drive Epidemiology strategy and studies across the spectrum of vaccine development? If so, this is an excellent opportunity to explore. Job Purpose To be responsible for Epidemiological studies within a large program or group of related programs (led by a senior epidemiologist) within the context of the GSK Vaccines process in order to ensure the high quality and on-time delivery of all epi data that will allow and support world-wide registration in compliance with the clinical and epi development plan, applicable good practices, and GSK Vaccines standard operating procedures (SOP). Key responsibilities: This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:...

Site Name: USA - Massachusetts - Waltham Posted Date: Aug 30 2024 Accountable to GRL and Global Regulatory TA Head for development of appropriate regional regulatory strategy(s) and for delivery according to plans. In conducting role, planning will be on a multiple year horizon, with delivery requiring extensive matrix working within GSK to VP level and representing GSK with at least the local regulatory agency. Work with the Early/Medicine Development Team (EDT/MDT) or GRL, to ensure a robust regulatory strategy is in place to support the development program to meet the needs of the key markets identified in the Integrated Asset plan and the Medicine Profile. Work closely with local / regional commercial team to secure best possible labelling commensurate with the available data. Lead interactions with local / regional regulatory authorities. Key Responsibilities: Proactively develop regulatory strategy that will deliver the needs of the local region(s), taking in...

Site Name: USA - Pennsylvania - Upper Providence, UK - Hertfordshire - Stevenage, USA - Massachusetts - Waltham, USA - North Carolina - Durham Posted Date: Aug 28 2024 We’re currently looking to expand our Bioanalysis and Biomarkers Platforms (BBP) department within Precision Medicine and seeking an Associate Director to join with strong exposure to PK and Biomarker Immunoassay end points. As the successful candidate, you’ll join GSK in a high visibility role where you’ll be at the forefront of medicine while managing the full life cycle of GSKs studies. Your skills as a bioanalytical scientist with drug development and regulatory understanding will help you working with internal and external partners to deliver bioanalytical endpoints for clinical studies across the GSK portfolio. You will serve as the subject matter expert (SME) on PK and Biomarkers data deliverables using various immunoassay platforms (e.g., ELISA, Gyros, MSD, Quanterix), and work closely with...

Site Name: USA - Pennsylvania - Upper Providence, USA - Massachusetts - Waltham, USA - North Carolina - Durham Posted Date: Aug 28 2024 GSK has an inspiring ambition: by uniting science, technology and talent we aim to positively impact the health of 2.5 billion people over the next ten years. We will get ahead of disease together with our R&D approach of focusing on the science of the immune system, human genetics and advanced technologies, such as functional genomics and AI/ML. We have an exciting opportunity at GSK for a highly motivated and experienced quantitative clinical pharmacologist to join our team supporting oncology therapeutic area as part of the global Clinical Pharmacology Modelling and Simulation (CPMS) department. GSK provides a supportive environment for scientists who are aspiring to learn, to contribute and to make impact on business decisions through innovation, expertise, and influence. As an Associate Director, CPMS, you will be part of a...

CSL Behring CSL Behring is a global biotechnology leader, guided by a promise to save and improve lives. Millions of people around the world are living with rare and serious medical conditions. CSL Behring is committed to delivering medicines that improve their lives. With operations in 35+ nations and ~ 30,000 employees worldwide, CSL is inspired to develop and deliver a broad range of lifesaving therapies to treat disorders such as hemophilia and primary immune deficiencies, and vaccines to prevent influenza. Our therapies are also used in cardiac surgery, organ transplantation and burn treatment. CSL is the parent company of CSL Behring, CSL Plasma, CSL Seqirus and CSL Vifor. CSL Behring is a global leader in the protein biotherapeutics industry, focused on bringing to market biotherapies used to treat serious and often rare conditions. Could you be our next AD, Clinical Portfolio Execution? This position is located in our King of Prussia PA, Waltham MA, Marburg Germany,...

Site Name: USA - Pennsylvania - Upper Providence, USA - Massachusetts - Waltham, USA - North Carolina - Durham Posted Date: Aug 23 2024 This is a 3 to 4 day per week onsite role and can be located in Collegeville PA, Waltham MA, or Durham NC. GSK is currently expanding its Biomarker & Bioanalytical Platforms (BBP) department and is seeking a Director, Immunogenicity Lead to join as an Immunogenicity Lead to support immunogenicity testing and reporting of biopharmaceutical, oligos and/or cell-based therapeutics candidates. As an Immunogenicity Lead , the high visibility role works closely with study project teams to determine immunogenicity risk, devise analytical strategies, contribute to protocol design, provide clinical data interpretation regarding the impact of immunogenicity on PK, safety, and efficacy. The successful candidate will contribute to regulatory documentation and respond to regulatory questions regarding immunogenicity. Additional activities include...