CSL 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 Senior Director, Regulatory Lead-Enabling Healthcare Technologies? The job is located in the King of Prussia PA Waltham,...

CSL 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 Senior Director, Regulatory Lead-Enabling Healthcare Technologies? The job is located in the King of Prussia PA Waltham,...

CSL The Global Regulatory CTA Therapeutic Area Lead is a recognized SME in CTA and is responsible for the global management of Clinical Trial Authorizations (CTAs) with the view to obtain CTA approvals in the fastest and most efficient way while ensuring quality documentation. The Senior GRSL develops the CTA submission strategy of large and/or complex projects, provides regulatory project management of CTAs and oversees the CTA submissions. This role is responsible for developing, maintaining and improving processes, drive development and improvement of new systems, solutions and procedures related to CTA activities and ensure compliance with international regulatory requirements and internal CTA procedures. The Senior GRSL supports Global Regulatory Affairs (GRA) vision of excellence regarding CTA activities for assigned projects through strategy, good scientific practice, integrity and consistent compliance with local regulatory standards. Interface with GRA TA leads and...

CSL Position Description Summary: The Senior Manager, Congress Planning will lead the logistical planning and execution for Above Market congresses, including management of accommodations and logistics associated with the congress and any ancillary events. They will own and manage the integrated congress project plan and co-ordinate the congress planning team in partnership with the congress owner. Provide subject matter expertise for all congress-related activities to the congress owner and functional leads. Collaborate with congress planners across business units in the delivery of co-led congresses as well as in sharing of best practices and opportunities for continuous improvement and innovation. Main Responsibilities & Accountabilities: Lead logistical planning and execution of successful congresses including negotiating convention exhibit space, contracts, hotel rooms, hospitality functions and show services; liaising with external professional society...

CSL The Senior Manager, Medical Operations, Pipeline works with the other Medical functions, in particular TA and Regional teams, to ensure timely execution of business operations including those relating to planning, budget, and execution. This role coordinates and leads the Medical Affairs Strategy Team for their assigned pipeline TA(s). Responsibilities: *Lead the implementation and maintenance of global templates for business processes, including annual plans, launch playbooks, budget worksheets in assigned TA(s)*Maintain current membership, charter, and standing agenda for Medical Affairs Strategy Teams*Ensure that assigned TA Medical Affairs Strategy Team(s) maintain membership of required functions, meet at defined cadence, and produce planned outputs*Implement business process calendar across assigned TA(s) to ensure insight generation, evidence generation planning, publication planning, and medical strategy documents are delivered on time and with the appropriate...

CSL The Manager, Medical Operations, Inline works with the other Medical functions, in particular TA and Regional teams, to ensure timely execution of business operations including those relating to planning, budget, and execution. This role coordinates and leads the Medical Affairs Strategy Team for their assigned inline TA(s). Responsibilities: *Lead the implementation and maintenance of global templates for business processes, including annual plans, launch playbooks, budget worksheets in assigned TA(s)*Maintain current membership, charter, and standing agenda for Medical Affairs Strategy Teams*Ensure that assigned TA Medical Affairs Strategy Team(s) maintain membership of required functions, meet at defined cadence, and produce planned outputs*Implement business process calendar across assigned TA(s) to ensure insight generation, evidence generation planning, publication planning, and medical strategy documents are delivered on time and with the appropriate inputs...

CSL The Manager, Medical Operations, Inline works with the other Medical functions, in particular TA and Regional teams, to ensure timely execution of business operations including those relating to planning, budget, and execution. This role coordinates and leads the Medical Affairs Strategy Team for their assigned inline TA(s). Responsibilities: *Lead the implementation and maintenance of global templates for business processes, including annual plans, launch playbooks, budget worksheets in assigned TA(s)*Maintain current membership, charter, and standing agenda for Medical Affairs Strategy Teams*Ensure that assigned TA Medical Affairs Strategy Team(s) maintain membership of required functions, meet at defined cadence, and produce planned outputs*Implement business process calendar across assigned TA(s) to ensure insight generation, evidence generation planning, publication planning, and medical strategy documents are delivered on time and with the appropriate inputs...

CSL As a true expert in the responsible TA, the Executive Director, will lead the development and execution of Medical Affairs strategies and tactics in support of the US market to demonstrate the value of CSL Behring's products in the respective Therapeutic Area (TA). She/He will provide the necessary up to date understanding of the US medical practice to internal CSL Behring stakeholders and align this knowledge with the global understanding that CSLB is aiming for in the field. This is internally and externally a highly visible role. The Specialty TA encompasses Hereditary Angioedema, Critical Care Acute Bleeding, and Congenital Respiratory Alpha 1 Antitrypsin Deficiency. The position holder will: Ensure that accurate and robust TA/product related medical-scientific knowledge and clinical expertise, is appropriately communicated through scientific exchange with Key Opinion Leaders (KOL's). Determine relevant gaps in the prioritized medical and scientific topics and create...

CSL 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 Associate Director, Global Regulatory Affairs? The job is located in our King of Prussia PA office. This is a hybrid...

Boehringer Ingelheim Compensation Data This position offers a base salary typically between $111,000.00 and $183,000.00. The position may be eligible for a role specific variable or performance based bonus and or other compensation elements. For an overview of our benefits please click here. Description As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, diversity and inclusion, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard...

CSL The Manager, Medical Operations, Inline works with the other Medical functions, in particular TA and Regional teams, to ensure timely execution of business operations including those relating to planning, budget, and execution. This role coordinates and leads the Medical Affairs Strategy Team for their assigned inline TA(s). Responsibilities: *Lead the implementation and maintenance of global templates for business processes, including annual plans, launch playbooks, budget worksheets in assigned TA(s)*Maintain current membership, charter, and standing agenda for Medical Affairs Strategy Teams*Ensure that assigned TA Medical Affairs Strategy Team(s) maintain membership of required functions, meet at defined cadence, and produce planned outputs*Implement business process calendar across assigned TA(s) to ensure insight generation, evidence generation planning, publication planning, and medical strategy documents are delivered on time and with the appropriate inputs...

Biogen Job Description The Strategy and Execution Lead (MLR Lead) for the Neuropsych Franchise is accountable for a high quality and efficient content approval process (ie. MLR) and will drive all operations for his/her respective brand/therapeutic area (TA), including both the front-line MLR review teams and the brand/TA-specific agile pod. This role will partner closely with Marketing and other business stakeholders from strategy development to initiate planning, channel strategies, new messaging, etc., ensuring that all concept and claim level thinking is shared with the pod for early collaboration and effective content execution. This role will also ensure the effective and efficient cascade of pod decisions through to front-line MLR review teams. The S&E Lead for Neuropsych Franchise currently provides support for a Biogen collaboration in a co-promotional capacity. As such, close collaboration with colleagues at both organizations is an essential responsibility of...

Pharmavite HELP US BRING THE GIFT OF HEALTH TO LIFE. Working at Pharmavite is an experience like no other. With a focus on complete nutrition for all, each endeavor is urgent and every day counts. You'll have the opportunity to work on the #1 selling national vitamin and supplement brand, Nature Made, as well as an exciting portfolio of other products that are shaping the future of the healthy living industry. Consumer-driven innovation, high quality products and a promising portfolio, all driven by a team with a shared sense of purpose -- that's Pharmavite. Join us to bring the gift of health to life. YOUR CONTRIBUTIONS: Develop a strategy to source candidates that may include a combination of advertising, contacting candidates directly, representing Pharmavite at recruiting events and other non-traditional and traditional sources. Sources passive candidates through extensive name generation research, relationship building, complex internet searches, existing talent...

Novartis Job Description Summary In partnership with Director PE TA drives systematic collaboration with the patient community and internal stakeholders to achieve strategic PE objectives and priorities by informing R&D programs that create value for patients, healthcare systems and Novartis. Implements and executes the PE Strategy in line with the Novartis Patient Focused Drug Development approach and the Decision Point Framework across the clinical development continuum for priority disease areas. The role reports to the Director PE TA and works closely with PE Science team, and Clinical Development and Development Unit teams within the assigned disease area(s). Partners internally with Early Patient Insights team in Biomedical Research, and US and International Comms & Patient Advocacy teams in Corporate Affairs. Partners externally with patient organizations, patient experts, patient advocates, patients, and caregivers. Job Description Major...

Site Name: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Cambridge MA, UK - London - New Oxford Street, USA - Maryland - Rockville Posted Date: Nov 21 2024 Established as a focused global function , Data Generation & Scientific Communications , is uniquely placed to help accelerate the successful integration of our medicines and vaccines into the healthcare pathway - we’re the ‘engine’ that brings our medical affairs strategies to life. Within this organization as the VP, Head of Global Real-World Evidence & Health Outcomes Research, Sulabha Ramachandran will be leading a team which incorporates the legacy VEO/Non-Interventional Studies capabilities teams under a newly evolved name that more closely reflects their purpose and the research they deliver. For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement and maintain market position. Specifically, evidence must be maintained throughout the...

Site Name: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Cambridge MA, UK - London - New Oxford Street, USA - Maryland - Rockville Posted Date: Nov 21 2024 Established as a focused global function , Data Generation & Scientific Communications , is uniquely placed to help accelerate the successful integration of our medicines and vaccines into the healthcare pathway - we’re the ‘engine’ that brings our medical affairs strategies to life. Within this organization as the VP, Head of Global Real-World Evidence & Health Outcomes Research, Sulabha Ramachandran will be leading a team which incorporates the legacy VEO/Non-Interventional Studies capabilities teams under a newly evolved name that more closely reflects their purpose and the research they deliver. For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement and maintain market position. Specifically, evidence must be maintained throughout the...

Site Name: USA - Pennsylvania - Upper Providence, Belgium-Wavre, Cambridge MA, UK - London - New Oxford Street, USA - Maryland - Rockville Posted Date: Nov 21 2024 Established as a focused global function , Data Generation & Scientific Communications , is uniquely placed to help accelerate the successful integration of our medicines and vaccines into the healthcare pathway - we’re the ‘engine’ that brings our medical affairs strategies to life. Within this organization as the VP, Head of Global Real-World Evidence & Health Outcomes Research, Sulabha Ramachandran will be leading a team which incorporates the legacy VEO/Non-Interventional Studies capabilities teams under a newly evolved name that more closely reflects their purpose and the research they deliver. For drugs to be successful, there must be robust health outcomes data to support launch optimization, reimbursement and maintain market position. Specifically, evidence must be maintained throughout the...

Site Name: USA - Pennsylvania - Upper Providence Posted Date: Nov 13 2024 The external environmental demands for robust evidence of the value of our assets continues to increase, with external stakeholders and decision makers increasingly demanding demonstration of the comparative clinical, economic, and humanistic benefits of our medicine at the time of launch, and thereafter. At the same time, the GSK organization is launching or soon to launch many new medicines, all of which will require significant leadership and evidence delivery from health outcomes to ensure successful translation of these reimbursement/payer requirements into our clinical development programs and delivery of the additional evidence that demonstrates value. To meet these needs, The Therapy Area (TA) Head, US, is responsible for the design and implementation of evidence generation activities in support of a GSK Therapy Area (TA) for the United States (US) business. It includes health outcomes...

Site Name: USA - Pennsylvania - Upper Providence Posted Date: Sep 23 2024 If you are an employee potentially impacted and at risk of redundancy, please add the following statement at the top of your CV: ‘ At Risk of Redundancy’. GlaxoSmithKline (GSK) is a global healthcare company committed to improving the quality of human life by enabling people to do more, feel better, and live longer. We discover, develop, and deliver innovative medicines, vaccines, and consumer healthcare products, and we are dedicated to our mission of helping people around the world. At GSK, we are dedicated to creating an inclusive and diverse workplace that reflects the communities we serve. We offer competitive compensation and benefits packages, opportunities for professional development, and a culture that values innovation, collaboration, and integrity. The Chief Patient Organization led by the Chief Patient Officer is accountable for bringing external perspectives of thought leaders,...

CSL Reporting to: Vice President, Commercial Co-Lead Hematology Therapeutic Area Position Description Summary The Senior Director Hematology, GCD Lead for Patient Blood Management (PBM) is responsible for the development and execution of global commercial strategies for pipeline products across the entire Hematology Therapeutic Area (TA), focusing on strategic execution of the PBM enterprise program in collaboration with CSL Vifor. This role is the key interface with R&D, ensuring a unified commercial voice. Main Responsibilities & Accountabilities - Develop and implement global commercial strategies for pipeline products and PBM enterprise program, ensuring optimal value and access. This includes developing strategic commercial plans containing brand vision and strategic imperatives. - Develop comprehensive "go to market" strategies, aligned with above market stakeholders and county leaders for all pipeline products in the TA, which includes...