28 current phd jobs found

Merck Job Description The Virology (HIV) Regional Medical Scientific Director is a credentialed (i.e., MD, PhD, DNP, Doctoral PA-C, or PharmD) therapeutic and disease area expert who engages in both scientific exchange and research support, when requested, with external scientific leaders and investigators in the medical and scientific community. Virology RMSDs provide Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to our Company and responds to scientific questions from SLs, including questions about our Company's products and data. Virology RMSDs are responsible for facilitating and developing peer-level relationships with scientific leaders in the external medical/scientific community including those investigators who have potential interest in participating in our Company's research studies. Virology RMSDs provide support for data generation activities including our Company's sponsored trials and our Company's...

Merck Job Description Job Summary This position leads the operational planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities Responsible for the operational planning, feasibility, and execution of a clinical trial.This may include: May serve as the clinical trial team lead May lead team in key study planning, development, and execution elements (e.g., data management deliverables, trial level plans/timelines, country/site selection, site materials, system updates, investigatormeeting planning, communication plans, preparation of status update reports, study close out activities). Leads team for timeline management, risk identification and mitigation,...

Merck Job Description Job Summary This position leads the operational planning and execution of one or more clinical trials or significant aspects thereof. In this position, you will have the opportunity to demonstrate your leadership and technical skills as part of a global, cross-functional team. You will apply project management, communication, and collaboration skills in support of our clinical trials. Job Responsibilities Responsible for the operational planning, feasibility, and execution of a clinical trial.This may include: May serve as the clinical trial team lead May lead team in key study planning, development, and execution elements (e.g., data management deliverables, trial level plans/timelines, country/site selection, site materials, system updates, investigatormeeting planning, communication plans, preparation of status update reports, study close out activities). Leads team for timeline management, risk identification and mitigation,...

Merck Job Description The Virology (HIV) Regional Medical Scientific Director is a credentialed (i.e., MD, PhD, DNP, Doctoral PA-C, or PharmD) therapeutic and disease area expert who engages in both scientific exchange and research support, when requested, with external scientific leaders and investigators in the medical and scientific community. Virology RMSDs provide Scientific Leaders (SLs) balanced, factual, scientific information about non-product areas of interest to our Company and responds to scientific questions from SLs, including questions about our Company's products and data. Virology RMSDs are responsible for facilitating and developing peer-level relationships with scientific leaders in the external medical/scientific community including those investigators who have potential interest in participating in our Company's research studies. Virology RMSDs provide support for data generation activities including our Company's sponsored trials and our Company's...

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...

Merck Job Description Support the Lead Epi Scientists by providing overall operational support for study conduct. Responsible for the coordination and execution of observational or non-interventional research studies (including Post Authorization studies), in compliance with Good Pharmacoepidemiology Practice (GPP) and Standard Operating Procedures (SOPs). Manages several complex activities and study types. Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. Primary responsibilities include: Operational planning and project management of epidemiology research studies Execution, and close out of primary data collection, chart review, database, and molecular epidemiology studies in addition to other activities Manage vendors...

Merck Job Description Role Summary The Associate Director, Global Scientific & Value Content-Healthcare Professional (AD, GSVC-HCP), position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. This mid-level, headquarters-based position involves engaging with key stakeholders and managing the development and implementation of GSVC content and plans. This position engages key stakeholders by proactively creating and adapting the Value & Implementation (V&I) Planning & Scientific Platform for GSVC Annual Product and Disease State Plans. This position develops and adapts GSVC plans for products and disease states aligned with V&I Plans. This position engages key stakeholders and incorporates medical insights into GSVC Annual Product Plans. This includes leading the development, review and communication of GSVC individual content within the...

Merck Job Description Role Summary The Associate Director, Global Scientific & Value Content-Healthcare Professional (AD, GSVC-HCP), position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. This mid-level, headquarters-based position involves engaging with key stakeholders and managing the development and implementation of GSVC content and plans. This position engages key stakeholders by proactively creating and adapting the Value & Implementation (V&I) Planning & Scientific Platform for GSVC Annual Product and Disease State Plans. This position develops and adapts GSVC plans for products and disease states aligned with V&I Plans. This position engages key stakeholders and incorporates medical insights into GSVC Annual Product Plans. This includes leading the development, review and communication of GSVC individual content within the...

Merck Job Description Role Summary The Associate Director, Global Scientific & Value Content-Healthcare Professional (AD, GSVC-HCP), position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. This mid-level, headquarters-based position involves engaging with key stakeholders and managing the development and implementation of GSVC content and plans. This position engages key stakeholders by proactively creating and adapting the Value & Implementation (V&I) Planning & Scientific Platform for GSVC Annual Product and Disease State Plans. This position develops and adapts GSVC plans for products and disease states aligned with V&I Plans. This position engages key stakeholders and incorporates medical insights into GSVC Annual Product Plans. This includes leading the development, review and communication of GSVC individual content within the...

Merck Job Description Role Summary The Associate Director, Global Scientific & Value Content-Healthcare Professional (AD, GSVC-HCP), position resides in the Value & Implementation (V&I) organization, which includes Global Medical and Scientific Affairs as well as Outcomes Research. This mid-level, headquarters-based position involves engaging with key stakeholders and managing the development and implementation of GSVC content and plans. This position engages key stakeholders by proactively creating and adapting the Value & Implementation (V&I) Planning & Scientific Platform for GSVC Annual Product and Disease State Plans. This position develops and adapts GSVC plans for products and disease states aligned with V&I Plans. This position engages key stakeholders and incorporates medical insights into GSVC Annual Product Plans. This includes leading the development, review and communication of GSVC individual content within the...

Merck Job Description This role plays a critical part in advancing our company's growing ophthalmology portfolio through the development, execution, and refinement of robust in vivo ophthalmic research models in preclinical species. The successful candidate will be a collaborative, scientifically rigorous problem-solver with the ability to translate ophthalmic expertise into impactful research solutions across early discovery and GLP environments. Hands-on, on-site laboratory work is an essential component of this position, along with demonstrated leadership, mentorship, and an unwavering commitment to personnel safety and animal welfare. Key Responsibilities: 1. Serve as a subject matter expertise to all aspects of the pipeline with a strong emphasis on ophthalmic research programs and the further development of existing and creating of new modalities and in vivo ophthalmic research models. 2. Design, conduct, or supervise ophthalmic animal research studies involving...

Merck Job Description Support the Lead Epi Scientists by providing overall operational support for study conduct. Responsible for the coordination and execution of observational or non-interventional research studies (including Post Authorization studies), in compliance with Good Pharmacoepidemiology Practice (GPP) and Standard Operating Procedures (SOPs). Manages several complex activities and study types. Our Clinical Research and Pharmacovigilance team push the boundaries of global healthcare through research and innovation. Through clinical trials and surveillance, we ensure the safety and efficacy of our existing and pipeline products to produce safe, effective, innovative medicine. Primary responsibilities include: Operational planning and project management of epidemiology research studies Execution, and close out of primary data collection, chart review, database, and molecular epidemiology studies in addition to other activities Manage vendors...

Merck Job Description This role plays a critical part in advancing our company's growing ophthalmology portfolio through the development, execution, and refinement of robust in vivo ophthalmic research models in preclinical species. The successful candidate will be a collaborative, scientifically rigorous problem-solver with the ability to translate ophthalmic expertise into impactful research solutions across early discovery and GLP environments. Hands-on, on-site laboratory work is an essential component of this position, along with demonstrated leadership, mentorship, and an unwavering commitment to personnel safety and animal welfare. Key Responsibilities: 1. Serve as a subject matter expertise to all aspects of the pipeline with a strong emphasis on ophthalmic research programs and the further development of existing and creating of new modalities and in vivo ophthalmic research models. 2. Design, conduct, or supervise ophthalmic animal research studies involving...

PerkinElmer Responsibilities Location Collegeville, Pennsylvania US Job ID REQ-056923 We are seeking a highly motivated and ambitious candidate to join the PerkinElmer OneSource Scientific Services team based at one of our customer sites in Collegeville, PA. The successful candidate will be working within the PerkinElmer Technical Lab Services (TLS) division and will be placed within a research unit at the customer site who have a focus on process engineering and modeling, supporting R&D and manufacturing activities and are at the forefront of developing innovative and life-changing medicines for patients. The candidate will work within a collaborative team environment across a diverse biotherapeutic portfolio within the company and can develop in PerkinElmer's scientific arena. The role will report to the PerkinElmer Regional TLS Leader and will be based at the GSK Upper Providence campus. Job Responsibilities Conduct laboratory experimentation and...

PerkinElmer Responsibilities Location Collegeville, Pennsylvania US Job ID REQ-056925 We are seeking a highly motivated and ambitious candidate to join the PerkinElmer OneSource Scientific Services team based at one of our customer sites in Collegeville, PA. The successful candidate will be working within the PerkinElmer Technical Lab Services (TLS) division and will be placed within a research unit at the customer site who have a focus on process engineering and modeling, supporting R&D and manufacturing activities and are at the forefront of developing innovative and life-changing medicines for patients. The candidate will work within a collaborative team environment across a diverse biotherapeutic portfolio within the company and can develop in PerkinElmer's scientific arena. The role will report to the PerkinElmer Regional TLS Leader and will be based at the GSK Upper Providence campus. Job Responsibilities Conduct laboratory experimentation and...

PerkinElmer Responsibilities Location Collegeville, Pennsylvania US Job ID REQ-056924 We are seeking a highly motivated and ambitious candidate to join the PerkinElmer OneSource Scientific Services team based at one of our customer sites in Collegeville, PA. The successful candidate will be working within the PerkinElmer Technical Lab Services (TLS) division and will be placed within a research unit at the customer site who have a focus on process engineering and modeling, supporting R&D and manufacturing activities and are at the forefront of developing innovative and life-changing medicines for patients. The candidate will work within a collaborative team environment across a diverse biotherapeutic portfolio within the company and can develop in PerkinElmer's scientific arena. The role will report to the PerkinElmer Regional TLS Leader and will be based at the GSK Upper Providence campus. Job Responsibilities Conduct laboratory experimentation and...

We Are Teva We’re Teva, a leading innovative biopharmaceutical company, enabled by a world-class generics business. Whether it’s innovating in the fields of neuroscience and immunology or delivering high-quality medicine worldwide, we’re dedicated to addressing patients’ needs now and in the future. Here, you will be part of a high-performing, inclusive culture that values fresh thinking and collaboration. You'll have the room to grow, the flexibility to balance life with work, and the opportunity to better health worldwide, together. The opportunity The Director, Global Regulatory Affairs, is a strategic role that will be responsible for developing, coordinating, and implementing regulatory strategies for drug development programs for innovative biologic and small molecule products as well as marketed products. This position will support the development and lifecycle management of therapies for conditions in Teva’s Immunology portfolio including dermatology,...

CSL As the Senior Director, Medical Affairs, you will lead the development and execution of Medical Affairs strategies and tactics to support the Coagulation Disease Area (DA). You will serve as the medical and scientific expert and represent current US medical practice to internal CSL Behring stakeholders. You will have a high awareness of patient needs, current therapeutic practices and new therapeutic trends in the US market. Essential to success is an outstanding partnership with the medical field team which will report to you through a Coagulation Field Medical Director; and, with Market Access, and Commercial to maximize the value proposition of the medicines in your portfolio. Externally, you will assist health care professionals and payers to optimize patient care and treatment outcomes through evidence-based decisions. You will: * Lead the US Medical team (Medical directors/scientists and Field MSL Lead) for the US Disease Area * Develop and execute annual US...

Merck Job Description Join Our Team as a Biologics Cell Culture Senior Scientist! Are you ready to take your career to the next level? We are seeking a strategic and technical scientist with expertise in cell culture development & commercialization to spearhead our ever growing and dynamic late-stage biologics pipeline within the expansive Biologics S&T portfolio. Why You'll Love This Role: As a Sr. Scientist in Biologics Cell Culture Commercialization, you'll be at the forefront of scientific advancement, providing strategic and tactical technical direction through cross-functional partnerships with key business units and customers. Your participation will be instrumental in supporting DS commercialization, process characterization, control strategy development, tech transfer to internal and external manufacturing sites, process validation, second generation process development and health authority licensure. You'll be supporting the charge in...

Merck Job Description Principal Scientist, Biologics, Sterile Drug Product Commercialization As part of Our Company's Manufacturing Division, the Sterile Drug Product Commercialization group provides the technical process leadership and laboratory capabilities for late stage and commercial drug product processes for biologics. It is the division's leader in sterile product and process development, responsible for late-stage commercialization activities including process scale up, technology transfer to internal and external sites, process validation, authoring of regulatory submissions and support of significant manufacturing investigations. The group is responsible for establishing the science, engineering and knowledge required for today's innovative and accelerated commercialization of biologics and combination products. We are seeking an experienced Principal Scientist to advance and commercialize biologics pipeline programs. As a member of the drug product...