Current jobs related to Sr. Manager, Clinical Scientist, Vaccines - Collegeville - Pfizer
-
Packaging Development Scientist
1 week ago
Collegeville, Indiana, United States GlaxoSmithKline Full timeAbout the Role:We are seeking a highly skilled Packaging Development Scientist to join our team at GlaxoSmithKline. As a key member of our Packaging, Device and Design Solutions team, you will be responsible for the development of Container Closure System (CCS) solutions within New Product Introduction (NPIs) progressing through Research & Development.Key...
-
Biological Research Scientist
2 weeks ago
Collegeville, Pennsylvania, United States Alphanumeric Systems Full timeBiologist - Bench ScientistWe are seeking a highly motivated and detail-oriented Biologist to join our team as a Bench Scientist. As a key member of our research team, you will be responsible for supporting the in vivo preclinical experimental and clinical needs of the group and scientific partners.Key Responsibilities:Support studies with the team according...
-
Packaging Development Scientist
1 week ago
Collegeville, Indiana, United States GlaxoSmithKline Full timeJob SummaryGSK's Packaging, Device and Design Solutions team is responsible for delivering robust, patient-centric devices and primary packaging solutions to support the effective delivery of novel pharmaceuticals across all modalities and routes of administration.As a Packaging Development Scientist, you will be part of a multi-skilled team of Engineers and...
-
Senior Manager, US Consumer Vaccination Program
2 weeks ago
Collegeville, Pennsylvania, United States Pfizer Full timeRole SummaryPfizer is seeking a Senior Manager to lead the US Consumer Vaccination Program, responsible for developing and executing marketing strategies to drive vaccination rates across the portfolio.Key ResponsibilitiesPartner with cross-functional teams to develop and optimize the VaxAssist tool and respiratory franchise consumer strategies.Support the...
-
Collegeville, Pennsylvania, United States GlaxoSmithKline Full timeAbout the RoleWe are seeking a highly skilled and experienced Team Leader to join our Modality Platform Technologies (MPT) group. As a key member of our team, you will be responsible for driving the creation and execution of our strategic objectives, managing a team of US-based scientists, and contributing to the development of novel modalities.Key...
-
Senior Manager, US Consumer VaxAssist
4 months ago
Collegeville, United States Pfizer Full timeROLE SUMMARY Vaccines is the only place in Pfizer where you can contribute to patients in a way like no other – you can help prevent sickness and disease. This is at the heart of what drives us every day and brings us great #Joy. It’s an exciting time to be in US Vaccines, with one of the strongest pipelines in the industry and with multiple product...
-
Collegeville, Pennsylvania, United States Pfizer Full timeJob SummaryPfizer is seeking a highly skilled and experienced Senior Manager to lead the development and execution of marketing strategies for our Vaccines and Respiratory portfolio. This role will be responsible for driving business growth and expanding our market share in the US.Key ResponsibilitiesDevelop and execute comprehensive marketing plans to...
-
Collegeville, Indiana, United States GlaxoSmithKline Full timeJob DescriptionJob Title: Medical Director Oncology Clinical DevelopmentJob Summary: We are seeking a highly skilled Medical Director to lead our Oncology Clinical Development team. The successful candidate will be responsible for advancing the development of our clinical portfolio and engaging with scientific and medical leaders to generate clinical...
-
Digital Sr. Manager Solution Engineer
1 month ago
Collegeville, Pennsylvania, United States Pfizer Full timeJob Title: Digital Sr. Manager Solution EngineerPfizer is seeking a highly skilled Digital Sr. Manager Solution Engineer to join our Digital Customer Experience Creation Center (C4). As a key member of our team, you will be responsible for leading the development and implementation of digital solutions that drive business growth and improve customer...
-
Global Oncology Clinical Development Manager
4 weeks ago
Collegeville, Pennsylvania, United States GlaxoSmithKline Full timeJob Title: Global Oncology Clinical Development ManagerWe are seeking an experienced Global Oncology Clinical Development Manager to join our team at GlaxoSmithKline. As a key member of our clinical operations team, you will be responsible for leading the global study delivery strategy, driving assessment and selection of vendors, and ensuring compliance...
-
Veterinary Scientist
4 weeks ago
Collegeville, United States Synectics Inc Full timeJob DescriptionJob DescriptionDescription:Primarily support the program of veterinary care and animal health and well-being Assists with study support for development of animal models and investigator researchAssists in behavioral assessment of animals and management of animal coloniesConducts daily observations, treatments and diagnostic procedures for a...
-
Collegeville, Pennsylvania, United States GlaxoSmithKline Full timeJob SummaryWe are seeking a highly skilled Senior Product Owner to join our team in Experiment Decision Capture. As a key member of our Scientific Data Capture group, you will be responsible for designing and delivering an innovative roadmap that enhances the user experience for lab scientists.Key ResponsibilitiesDevelop and maintain a deep understanding of...
-
Collegeville, Pennsylvania, United States GlaxoSmithKline Full timeAbout the RoleWe are seeking a highly skilled Senior Product Owner to join our Scientific Data Capture team. As a key member of our team, you will be responsible for designing and delivering an innovative roadmap that enhances the laboratory scientist experience and produces high-quality, standardized, and contextualized data.Key ResponsibilitiesDevelop and...
-
Research Scientist
2 weeks ago
Collegeville, Pennsylvania, United States Thermo Fisher Scientific Full timeJob SummaryThermo Fisher Scientific is seeking a highly skilled Associate Research Scientist to join our team. As a key member of our Analytical Services team, you will be responsible for performing routine to complex sample preparation and analysis procedures to quantitatively measure pharmaceutical and biopharmaceutical compounds in various formulations...
-
Medical Director
7 days ago
Collegeville, Indiana, United States GlaxoSmithKline Full timeJob SummaryThe Medical Director - Oncology Clinical Development will lead clinical research activities to advance the development of GSK's oncology portfolio. This role will report to the Executive Medical Director, Clinical Development Lead (CDL), Oncology Clinical Development.Key ResponsibilitiesCollaborate with physicians, scientists, regulatory...
-
Clinical Psychologist Manager
2 weeks ago
Collegeville, Pennsylvania, United States Staff Today Inc Full timeJob SummaryStaff Today Inc is seeking a highly skilled Clinical Psychologist Manager to lead our Psychology Department at a State Correctional Institution. The ideal candidate will have a strong background in clinical supervision, program management, and psychological testing. Key ResponsibilitiesProvide clinical supervision to front-line Master's level...
-
Clinical Development Director
1 week ago
Collegeville, Indiana, United States GlaxoSmithKline Full timeAccelerate Business Performance across and drive global operational support as a Clinical Development Director at GlaxoSmithKline.The Clinical Sciences Lead is the single point of accountability for the development of the scientific design, medical governance, and interpretation of results of a study. The study designed is expected to fulfill a strategic...
-
Senior Scientist, Process Development
4 weeks ago
Collegeville, Pennsylvania, United States PerkinElmer Full timeJob SummaryWe are seeking a highly skilled Principal Scientist, Process Engineering to join our team at PerkinElmer. The successful candidate will be responsible for conducting laboratory experimentation and analytical testing of putative formulations and drug product manufacturing. This is a full-time position with a competitive salary range of $87,360.00...
-
Patent Attorney
4 weeks ago
Collegeville, Pennsylvania, United States GlaxoSmithKline Full timePatent Counsel Role at GSKWe are seeking a highly skilled Patent Counsel to join our team at GlaxoSmithKline (GSK). As a Patent Counsel, you will play a critical role in building and managing patent portfolios related to cutting-edge pharmaceutical products.Key Responsibilities:Independently build and manage patent portfolios related to pharmaceutical...
-
Global Oncology Clinical Development Manager
2 weeks ago
Collegeville, Pennsylvania, United States GlaxoSmithKline Full timeJob SummaryWe are seeking a highly experienced Clinical Development Manager to lead our Oncology clinical trials. The successful candidate will have a strong background in clinical operations and a proven track record of delivering high-quality studies on time and within budget.The Clinical Development Manager will be responsible for planning and executing...
Sr. Manager, Clinical Scientist, Vaccines
2 months ago
The Clinical Scientist (CS) - Sr. Manager will support clinical epidemiology study execution for multiple studies for one or more vaccine programs. In collaboration with Scientific Affairs (SA) / Clinical Epidemiology, Biostatistics group and Clinical Affairs (CA) Operations, the CS is responsible for execution and project management of their studies which may vary and include both Pfizer-sponsored studies and externally-sponsored Research Collaborations. The CS position is a global position and may support projects in the US, Europe and Developed Markets. The CS works in a matrix organization and interacts with Epidemiologists, Biostatisticians, Clinical Operations, Global and Regional Medical/Scientific Affairs, Pfizer Research and Development clinical and laboratory groups, and external team members. Study responsibilities include core study document development (e.g., protocols, informed consent documents, case report forms, etc.), data review, oversight of study conduct activities with a focus on compliance, quality, safety, data integrity, and in alignment with company values. The CS, in partnership with Medical/Scientific Affairs, also supports the development and execution of the epidemiological plans and study strategies in support of the Clinical Development and Life Cycle plans. Data generated by epidemiological studies is critical evidence needed to support clinical development, to obtain optimum Vaccine Technical Committee recommendations, and to develop studies for post-licensure vaccine effectiveness regulatory commitments.
ROLE RESPONSIBILITIES
The CS is responsible for supporting end-to-end study activities for multiple epidemiological studies across various SOPs (for each study):
Protocol and study training - independently drafts study concepts/synopses, protocol and amendments of moderate complexity in collaboration with Scientific Affairs Lead, Biostatistician, and other relevant team members (e.g., VRD, external collaborators). Prepares and provides clinical protocol training materials to internal and external study team members. Ensures proper compliance and governance processes are followed in developing and approving study protocols. Drafts and/or reviews informed consent documents and supports the preparation of other clinical study documents as needed.Data collection, review and interpretation - provide clinical input on case report form development in accordance with clinical protocol requirements. Provide input on study data review plans and perform clinical data review in collaboration with Scientific Affairs Lead. Contribute to and participate in data interpretation and analyses discussions.Study oversight - in collaboration with Scientific Affairs Lead, and other operational study team members, provide clinical guidance and oversight during the execution of the study to ensure protocol compliance, issue resolution, patient safety, and data integrity. Maintain appropriate study documentation (e.g., meeting minutes, decision logs)Safety review and communication - depending on the nature of the study and its associated safety reporting requirements, conduct appropriate safety data review.Regulatory document, study report, and publication preparation and review - provide input on study-related regulatory documentation/correspondence. Provide clinical and operational content for clinical study reports and publications as appropriate. Lead efforts and responses for study audits (depending on study type).Epidemiologic study / program implementation - depending on the nature of the study (i.e., which SOP applies), may manage vendors (e.g., CRO, laboratory, supplies), develop and/or review study budgets, develop and maintain study timelines, track study deliverables, review protocol deviations and manage compliance issue follow-up and remediation
BASIC QUALIFICATIONS
Candidate demonstrates a breadth of diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful outcomes and create business impact.
BA/BS Degree in life sciences or health related field with 7+ years practical experience or MS/MPH with 5+ years; PharmD/PHD with 2+ yearsHas experience planning and managing epidemiology studiesHas experience participating in and leading operational study teamsHas ability to work independently with moderate supervisionExperience in research on infectious disease and/or vaccinesDemonstrated ability and experience with integrating and summarizing medical / scientific concepts in study protocols and other clinical documentsHas advanced knowledge of the clinical research process and Good Clinical Practices from previous employment experience in the clinical research fieldHas independently authored clinical protocols and other clinical study documentsHas working knowledge of statistics, data analysis, and data interpretationHas experience in managing external vendors for clinical and/or epidemiological studiesFluent in English writing, reading, and speaking and has exceptional written and oral communication and cross-functional collaborative skills.
PREFERRED QUALIFICATIONS
MS or PhD preferredHas experience in working in a global settingIs proficient in MS Word, Excel, and PowerPointPrior infectious disease, microbiological or infection control experienceHas worked in Industry
Last date to apply: September 19, 2024.
The annual base salary for this position ranges from $131,200.00 to $218,600.00. In addition, this position is eligible for participation in Pfizer's Global Performance Plan with a bonus target of 17.5% of the base salary and eligibility to participate in our share based long term incentive program. We offer comprehensive and generous benefits and programs to help our colleagues lead healthy lives and to support each of life's moments. Benefits offered include a 401(k) plan with Pfizer Matching Contributions and an additional Pfizer Retirement Savings Contribution, paid vacation, holiday and personal days, paid caregiver/parental and medical leave, and health benefits to include medical, prescription drug, dental and vision coverage. Learn more at Pfizer Candidate Site - U.S. Benefits | (uscandidates.mypfizerbenefits.com). Pfizer compensation structures and benefit packages are aligned based on the location of hire. The United States salary range provided does not apply to Tampa, FL or any location outside of the United States.
Relocation assistance may be available based on business needs and/or eligibility.
Sunshine Act
Pfizer reports payments and other transfers of value to health care providers as required by federal and state transparency laws and implementing regulations. These laws and regulations require Pfizer to provide government agencies with information such as a health care provider's name, address and the type of payments or other value received, generally for public disclosure. Subject to further legal review and statutory or regulatory clarification, which Pfizer intends to pursue, reimbursement of recruiting expenses for licensed physicians may constitute a reportable transfer of value under the federal transparency law commonly known as the Sunshine Act. Therefore, if you are a licensed physician who incurs recruiting expenses as a result of interviewing with Pfizer that we pay or reimburse, your name, address and the amount of payments made currently will be reported to the government. If you have questions regarding this matter, please do not hesitate to contact your Talent Acquisition representative.
EEO & Employment Eligibility
Pfizer is committed to equal opportunity in the terms and conditions of employment for all employees and job applicants without regard to race, color, religion, sex, sexual orientation, age, gender identity or gender expression, national origin, disability or veteran status. Pfizer also complies with all applicable national, state and local laws governing nondiscrimination in employment as well as work authorization and employment eligibility verification requirements of the Immigration and Nationality Act and IRCA. Pfizer is an E-Verify employer. This position requires permanent work authorization in the United States.
Medical
#LI-PFE
