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Billable consultant 60 80% Accountable for oversight of a consultancy team to assure team members are sufficiently billable 80% of time in the office and profitable through maintenance of client relationships and writing of proposals. Is part of the QSS US leadership team (LT) together with the regional Senior Vice President (SVP). Accountable for organizational structure and operations of the con
Posted Today
The Technical Support Analyst combines technical knowledge with presentation skills to provide advice both internally and externally. An effective Technical Support Analyst has a knack for solving complex problems in addition to having good communications and customer relationship skills. A level headed person who can talk customers through complex technical solutions. The Technical Support Analys
Posted 1 day ago
Our Pharmacometricians are responsible for providing expertise into clinical development plans, including the design, conduct, and interpretation of relevant clinical pharmacology and PK/PD studies. Qualified candidates will have the ability to work on a variety of therapeutic indications and data types with an adequate understanding of applied population PK and PK/PD modeling and simulation to su
Posted 3 days ago
In this role you will play a pivotal part in supporting and leading client early and late clinical development engagements by providing scientific and strategic pharmacometrics input that addresses key questions in their development programs, clinical study design considerations, model informed drug development strategies, as well as interactions with and submissions to regulatory authorities. Add
Posted 7 days ago
Lead or participate in a project team which may be led by a Principal Regulatory Writer or Associate Principal Regulatory Writer, or independently lead Narrative projects for clients Author and oversee authoring of narratives per client specifications, templates, style guides, and other guidance documents Author documents per regulatory authority guidelines and requirements Act as client advisor,
Posted 8 days ago
Certara USA, Inc.
- Orlando, FL / Wilmington, DE / San Diego, CA / 4 more...
Lead or participate in a project team which may be led by a Principal Regulatory Writer or Associate Principal Regulatory Writer Author documents per client specifications, templates, style guides, and other guidance documents Author documents per regulatory authority guidelines and requirements Act as client advisor, working with all parties to lead development of strategies for organizing and pr
Posted 8 days ago
Lead or participate in a project team which may be led by a Principal Regulatory Writer or Associate Principal Regulatory Writer, or independently lead Narrative projects for clients Author and oversee authoring of narratives per client specifications, templates, style guides, and other guidance documents Author documents per regulatory authority guidelines and requirements Act as client advisor,
Posted 8 days ago
Certara USA, Inc.
- Wilmington, DE / Princeton, NJ
Location Work From Home in the US or from one of our office locations (Princeton, NJ) Certara is the global leader in advancing modern, efficient drug development. We provide proven modeling & simulation, regulatory and real world value assessment software platforms and services. In partnership with our clients, we help reduce clinical trial burden, accelerate regulatory approval and increase
Posted 9 days ago
Establish multiple level contacts within assigned accounts by presenting to, consulting with, and cultivating relationships at all buying levels. Qualify companies and contacts to understand the customer’s key needs/challenges through identification, discovery, planning and account/customer qualifications. Manage and support distributors by successfully initiating client contacts, generate n
Posted 9 days ago
Lead and provide strategic insight on document quality related tasks including but not limited to quality control reviews using Word features/functions using internal/client templates/toolbars Liaise with KAMs document level publishing Proficiency in techniques to be able to offer services and proactively resolve issues to a client directly in more complex engagements (as a super user or client le
Posted 11 days ago
Certara USA, Inc.
- Philadelphia, PA / San Diego, CA / Princeton, NJ / 2 more...
Associate may conduct any or multiple of the following activities in the areas of PK and data management PK Associate PK tasks such as NCA, entry level Modeling and Simulation, creation of TFL, authoring of CSR PK sections, ADA summaries. Performs noncompartmental analyses (NCA), creation of tables, figures and listings (TFL), authoring of pharmacokinetic (PK) sections in Clinical Study Report, Re
Posted 11 days ago
Certara USA, Inc.
- Raleigh, NC / Princeton, NJ
The Operations Specialist will have responsibility for business operations activities for the iDD Division. The individual may be tasked with providing support across a variety of operations tasks, including, but not limited to, invoicing, expense management, reporting, onboarding, etc. Operations specialists may also serve as process facilitators positional focus includes resource management and
Posted 11 days ago
Certara USA, Inc.
- Princeton, NJ / Menlo Park, CA
Our Pharmacometricians are responsible for supporting quantitative decision making in drug development through the development and application of population PK, PK/PD, exposure response and other models. Qualified candidates will have the ability to work on a variety of therapeutic indications and data types and must be experts in applied Population PK, PK/PD, and/or exposure response modelling an
Posted 11 days ago
Lead and provide strategic insight on document quality related tasks including but not limited to quality control reviews using Word features/functions using internal/client templates/toolbars Liaise with KAMs document level publishing Proficiency in techniques to be able to offer services and proactively resolve issues to a client directly in more complex engagements (as a super user or client le
Posted 15 days ago
Demonstrate strong proficiency with quality control review, including verification of document against source, verification of internal consistency, verification of grammar based on understanding of grammar rules and begin to train others in this knowledge Expertly perform formatting techniques consistent with company guidelines, including but not limited to application of styles, table insertion,
Posted 15 days ago
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