22 pharmacy manager jobs found

CSL CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director, Regional Regulatory Lead-US? The job is in our King of Prussia, PA or Waltham MA office. This is a hybrid position and is onsite three days a week. You will report to the Director Global Regulatory Lead. You are a member of the respective GRA GRS Therapeutic Area and contributes to the vision and goals of CSL as: Regulatory leaders who leverage regional regulatory experience / expertise to influence and actively contribute to an innovative, scientifically sound, global, integrated regulatory vision / strategies for assigned product/s with a patient centric-focus, leveraging...

Wellington Management About Us Wellington Management offers comprehensive investment management capabilities that span nearly all segments of the global capital markets. Our investment solutions, tailored to the unique return and risk objectives of institutional clients in more than 60 countries, draw on a robust body of proprietary research and a collaborative culture that encourages independent thought and healthy debate. As a private partnership, we believe our ownership structure fosters a long-term view that aligns our perspectives with those of our clients. About the Role THE POSITION We are currently seeking to recruit an Equity Research Analyst (Analyst) to join our established Value Equity Income Portfolio Management team. This team manages approximately $74 billion in US large cap value and equity income strategies. The team selects stocks bottom-up, across the large and mid-cap spectrum, without regard to benchmark, based on intensive fundamental...

Wellington Management About Us Wellington Management offers comprehensive investment management capabilities that span nearly all segments of the global capital markets. Our investment solutions, tailored to the unique return and risk objectives of institutional clients in more than 60 countries, draw on a robust body of proprietary research and a collaborative culture that encourages independent thought and healthy debate. As a private partnership, we believe our ownership structure fosters a long-term view that aligns our perspectives with those of our clients. About the Role THE POSITION We are currently seeking to recruit an Equity Research Analyst (Analyst) to join our established Value Equity Income Portfolio Management team. This team manages approximately $74 billion in US large cap value and equity income strategies. The team selects stocks bottom-up, across the large and mid-cap spectrum, without regard to benchmark, based on intensive fundamental...

Merck Job Description The Developmental and Reproductive Toxicology (DART) group within Nonclinical Drug Safety (NDS), is seeking a highly motivated person with strong technical skills and diligence to conduct in vivo studies as part of a collaborative team supporting drug development programs. The successful candidate will perform in vivo administration of compound, data collection, cesarean sections with fetal examination, and necropsies under limited supervision. The position requires the ability to maintain neat, concise, and accurate records, along with good oral communication skills. The successful candidate will also train and work cross-functionally, assisting other areas within NDS. This position is for a 5-day work week, including coverage of weekends and Holidays on a rotational basis. Specific responsibilities include but are not limited to: Perform assigned tasks that include dose administration by various routes; recording of body weights, food...

Merck Job Description Associate Director, US Pharma, New Products Marketing This is an exciting opportunity for a highly motivated individual to play a critical role in the US commercial development of our Company's pipeline assets. The role will report directly to the US Pharma Marketing Leader for New Products and has the primary responsibilities of developing the US market strategy to shape the environment for successful new product launches. The role will work across the enterprise to define value evidence and clinical development needs to support US commercial forecasts. As new products progress into Ph2B/3 the role is responsible for execution of market shaping strategies and measuring impact leveraging agile ways of working to evolve the strategy. Ideally, the candidate will have in-depth knowledge of the US market, strong scientific acumen, US policy/ advocacy experience and understanding of developing marketing strategies for new products. Primary...

Merck Job Description TranslationalMedicine(TMed)drivesearly clinical development of novel therapeuticsby partneringwith Discovery Sciences and Late-Stage Clinical Researchto translatescientific discoveriesinto human proof-of-conceptandadvancethe most promising candidates through the pipelineto patients. Wedesign and execute clinical pharmacology strategiesspanningfirst-in-humanstudiesthrough proof-of-biology/proof-of-conceptandintolate-stage development,supportingworldwide marketingapplicationsand lifecycle management. In a competitive externallandscapeand fast-pacedinternalenvironment, this positionprovidesbothstrategicandoperationalleadership acrossearlyimmunologyprograms,ensuringtimely, high-quality execution of clinical studies and clinical pharmacology strategies worldwide.The successful candidate willtelescope betweenstrategy and hands-onexecution acrossa portfolio of diverse modalities (e.g. peptides, small molecules, biologics), andpartner cross-functionally to...

Merck Job Description TranslationalMedicine(TMed)drivesearly clinical development of novel therapeuticsby partneringwith Discovery Sciences and Late-Stage Clinical Researchto translatescientific discoveriesinto human proof-of-conceptandadvancethe most promising candidates through the pipelineto patients. Wedesign and execute clinical pharmacology strategiesspanningfirst-in-humanstudiesthrough proof-of-biology/proof-of-conceptandintolate-stage development,supportingworldwide marketingapplicationsand lifecycle management. In a competitive externallandscapeand fast-pacedinternalenvironment, this positionprovidesbothstrategicandoperationalleadership acrossearlyimmunologyprograms,ensuringtimely, high-quality execution of clinical studies and clinical pharmacology strategies worldwide.The successful candidate willtelescope betweenstrategy and hands-onexecution acrossa portfolio of diverse modalities (e.g. peptides, small molecules, biologics), andpartner cross-functionally to...

Merck Job Description Associate Director, US Pharma, New Products Marketing This is an exciting opportunity for a highly motivated individual to play a critical role in the US commercial development of our Company's pipeline assets. The role will report directly to the US Pharma Marketing Leader for New Products and has the primary responsibilities of developing the US market strategy to shape the environment for successful new product launches. The role will work across the enterprise to define value evidence and clinical development needs to support US commercial forecasts. As new products progress into Ph2B/3 the role is responsible for execution of market shaping strategies and measuring impact leveraging agile ways of working to evolve the strategy. Ideally, the candidate will have in-depth knowledge of the US market, strong scientific acumen, US policy/ advocacy experience and understanding of developing marketing strategies for new products. Primary...

Merck Job Description The Developmental and Reproductive Toxicology (DART) group within Nonclinical Drug Safety (NDS), is seeking a highly motivated person with strong technical skills and diligence to conduct in vivo studies as part of a collaborative team supporting drug development programs. The successful candidate will perform in vivo administration of compound, data collection, cesarean sections with fetal examination, and necropsies under limited supervision. The position requires the ability to maintain neat, concise, and accurate records, along with good oral communication skills. The successful candidate will also train and work cross-functionally, assisting other areas within NDS. This position is for a 5-day work week, including coverage of weekends and Holidays on a rotational basis. Specific responsibilities include but are not limited to: Perform assigned tasks that include dose administration by various routes; recording of body weights, food...

Merck Job Description Our Manufacturing Division is a team of dedicated, energetic individuals who are committed to being the most trusted supplier of pharmaceuticals and health products worldwide. Our facilities, along with our external contractors, suppliers, and partners, comprise an interdependent global manufacturing network that's committed to delivering a compliant, reliable supply to customers and patients on time, every time, across the globe. Our Supply Chain team ensures inventory is consistently available to meet customer demand. We coordinate all aspects of supply through supply planning, sourcing, making, inventory management, packaging and delivery. We partner across the Marketing, Finance, and Manufacturing organizations to build a robust demand and supply plan and ensure we get products to the right customer, at the place, at the right time. The Demand Fulfillment Planner is responsible for managing the supply chain for a set of products to ensure...

Biogen In this field based, specialty sales representative position you will be called upon to sell our Neurology products with key stakeholders in the Multiple Sclerosis community: including Neurologists, allied health professionals, and local MS chapters. The Harrisburg territory also includes Hershey, Lancaster and York. The idea candidate will live in the Harrisburg area. The Sr. Territory Business Manager is responsible for developing and executing on sales plans for their assigned territory. Candidates can be considered for Sr. Territory Business Manager or Territory Business Manager base on qualification outlined below. What You'll Do You will convey complex clinical and reimbursement information to customers and key stakeholders regarding Biogen products. You must be able to utilize exemplary interpersonal skills and directed probing to uncover and address the customer's educational needs. This position works closely with cross functional peers to help...

CSL CSL is a leading global biotechnology company with a dynamic portfolio of lifesaving medicines, including those that treat hemophilia and immune deficiencies, vaccines to prevent influenza, and therapies in iron deficiency, dialysis, and nephrology. Since our start in 1916, we have been driven by our promise to save lives using the latest technologies. Today, CSL - including our three businesses, CSL Behring, CSL Seqirus and CSL Vifor - provides lifesaving products to patients in more than 100 countries and employs 32,000 people. Our unique combination of commercial strength, R&D focus and operational excellence enables us to identify, develop and deliver innovations so our patients can live life to the fullest. Program Experience: CSL's Internship Program is a hands-on experience that showcases the daily innovation and operations of a leading biotechnology company. Our environment is collaborative, global, and purpose-driven. The 12-week experience will immerse...

CSL The Lead, Global Regulatory Affairs Device is responsible for: Developing, coordinating and implementing global Software as a Medical Device regulatory strategies for new combination and standalone medical devices. Ensure worldwide regulatory device compliance and successful market access across all regions. Closely collaborate with internal stakeholders on regulatory strategy issues, develop approaches to address regulatory and compliance matters, serve as primary liaison to the US FDA for device matters, and closely work regional regulatory staff to engage with international health authorities. Represening CSL in official device regulatory capacities and acting as an authorized official or responsible person in interactions with regulatory agencies. This role promotes strong cross-functional collaboration and effective communication across Global Operations, Plasma Operations, R&D, Global Regulatory Affairs, and other relevant CSL business functions to...

CSL The Lead, Global Regulatory Affairs Device is responsible for: Partnering closely with R&D, Manufacturing, Operations, Quality, and Regulatory Affairs stakeholders to address regulatory strategy challenges and deliver innovative, timely regulatory solutions that meet evolving device regulatory and compliance requirements for plasmapheresis devices, drug device combination products, standalone drug delivery devices, and ancillary devices. Ensure worldwide regulatory device compliance and successful market access across all regions. Closely collaborate with internal stakeholders on regulatory strategy issues, develop approaches to address regulatory and compliance matters, serve as primary liaison to the US FDA for device matters, and closely work regional regulatory staff to engage with international health authorities. Represening CSL in official device regulatory capacities and acting as an authorized official or responsible person in interactions with...

CSL Position Purpose The Head of Global Regulatory Affairs Device is responsible for: Providing strategic leadership and operational oversight for the Global Regulatory Affairs Device function. Leading the global regulatory strategy and execution for CLS's medical device portfolio during development and post-approval lifecycle, including plasmapheresis devices, blood establishment computer software (BECS), drug device combination products, standalone drug delivery devices, ancillary devices, and software as/in a medical device (SaMD/SiMD). Ensure worldwide regulatory device compliance and successful market access across all regions. Closely collaborate with internal stakeholders on regulatory strategy issues, develop approaches to address regulatory and compliance matters, serve as primary liaison to the US FDA for device matters, and closely work regional regulatory staff to engage with international health authorities. Represening CSL in official...

CSL The Global Regulatory Affairs CMC - Decision Support Lead is responsible for: Providing comprehensive administrative support to the Head of Global Regulatory Affairs CMC to enable the Head of Global Regulatory Affairs CMC to focus on strategic priorities and organizational leadership. This role requires exceptional attention to detail, strong communication skills, maintaining the highest level of confidentiality, and the ability to manage multiple priorities simultaneously. Providing targeted administrative support to the Global Regulatory Affairs CMC leadership team, ensuring the efficient operation of departmental activities. Tracks departmental business actions, goals, objectives, KPIs, and commitments to internal stakeholders. Supports the Head of Global Regulatory Affairs CMC in department-wide resource planning and forecasting through data-driven resource analysis. Partners with finance, HR, and project managers to support workforce planning, hiring...

CSL Reports to: Associate Director, Clinical Trial Business Operations Position Summary The Senior Manager, Clinical Trial Business Operations (CTBO) oversees CRO execution of investigator site budgets, contracts, site payments, and ICF deliverables. This role is also responsible for coordinating clinical trial insurance needs and supporting Sunshine Act/transparency reporting requirements. The Senior Manager ensures operational consistency, manages escalations, and contributes to compliance, quality, and governance activities. Key Responsibilities CRO Oversight Review and oversee CRO work related to budgets, contracts, payments, and ICFs. Ensure accuracy, quality, and alignment with internal templates, processes, and parameters. Provide operational guidance to CRO teams to ensure consistency across regions and studies. Escalation & Issue Management Manage escalations exceeding CRO negotiation authority. Partner with Clinical Operations,...

CSL The Associate Director (AD), Biostatistics, leads the full scope of statistical contribution to a clinical development program. The AD provides statistical strategies for the clinical trials and regulatory submissions, and is accountable for the statistical deliverables within the program. 1 Lead full scope of Biostatistics conduct for the responsible program within a therapeutic area. Define statistical strategy and ensure appropriate statistical methodologies applied to study design and data analysis for clinical trials and regulatory submissions 2 Influence and contribute to clinical development plans, collaborate with cross-functional team for governance reviews. Lead statistical strategy for planning and study execution (member of Study Executive Team, Clinical Development Team) and quantitative evaluation to clinical trials, regulatory submissions, and related documents. 3 Provide statistical thought partnership for innovative study design and clinical development...

CSL Job Title: ERP Platform & Applications - SAP Basis Lead Role Overview The SAP Basis Lead is responsible for the technical integrity, reliability, performance, and lifecycle management of the enterprise SAP ecosystem across cloud (RISE PCE, BTP) and other platforms. Operating within an Agile/SAFe delivery model, this role ensures that the SAP technical landscape supports business operations, transformation initiatives, and platform evolution. The SAP Basis Lead works closely with product leaders, architects, managed service providers (MSPs), cybersecurity teams, and business stakeholders to deliver a secure, stable, and scalable platform. Key Responsibilities Strategic & Technical Leadership Own the technical strategy and roadmap for SAP Basis services within the ERP Platform & Applications domain. Ensure enterprise alignment with SAP best practices, clean-core principles, and upgrade-safe designs. Integrate SAP Activate phases with...