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Katalyst HLS
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May 18th - HIV Vaccine Awareness Day, 2018
"No Vaccine Can Prevent HIV"

+Katalyst HealthCares & Life Sciences
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Skills/Knowledge Required: Extensive experience writing all types of clinical and regulatory documents for worldwide use, expertise in the Oncology therapeutic areas, experience in worldwide registration studies and large studies, understanding and good…
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Clinical Narrative Writer Katalyst HLS - Skills/Knowledge Required: Extensive experience writing all types of clinical and regulatory documents for worldwide use, expertise in the Oncology therapeutic areas, experience in worldwide registration studies and large studies, understanding and good use of all study documents. Protocol, SAP, CRF, SMQs, expertise in MS WORD, including the ability to solve technical problems with WORD templates, excellent grammatical and communication skills. Both written and oral, knowledge of FDA and ICH guidelines, ability to work with multiple complex projects at a time, ability to anticipate and resolve problems working independently, Experience working with automated data solutions in clinical documents, experience working with CROs, proficiency in data interpretation, sound organizational skills. Experience interfacing with multiple teams, and proven ability to problem solve and identify inconsistencies or inaccuracies in data listings.
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Roles & Responsibilities Designs clinical studies, formulates and conducts scientific investigations, and due diligence studies related to Client products. Interprets and presents results. Prepares technical reports, abstracts. Identifies appropriate…
Clinical Project Lead Katalyst HLS
Clinical Project Lead Katalyst HLS
katalysthls.wordpress.com
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Clinical Project Lead Katalyst HLS - Roles & Responsibilities Designs clinical studies, formulates and conducts scientific investigations, and due diligence studies related to Client products. Interprets and presents results. Prepares technical reports, abstracts. Identifies appropriate clinical and/or other defined testing to address clinical risks for product changes. Develops safety and efficacy requirements and a clinical test plan to address S&E, Regulatory and Marketing requirements products and gains functional approval of such. With the support of the MA team, ensures safety, efficacy and clinical utility of the product, technology and related labelling/promotional material.
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Roles & Responsibilities: At Excite, we want you to succeed. We want to help you reach your goals and find a satisfying and challenging work environment. For the Clinical Data Analyst position, you should meet the following criteria: Knowledge of standard…
Clinical Data Analyst Katalyst HLS
Clinical Data Analyst Katalyst HLS
katalysthls.wordpress.com
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Clinical Data Analyst Katalyst HLS - Roles & Responsibilities: At Excite, we want you to succeed. We want to help you reach your goals and find a satisfying and challenging work environment. For the Clinical Data Analyst position, you should meet the following criteria: Knowledge of standard business intelligence tools and ability to construct and interpret SQL statements Experience with statistical analysis, including application of statistical methods Experience with enterprise data warehouse structure and source systems Soarian experience (Clinicals, Financials, and Web Publishing)
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Job Responsibilities: Develop and validate SAS ® programs to produce high-quality deliverables within set timelines in accordance with company and regulatory requirements. The deliverables include SDTM and ADaM datasets, tables, listings and figures.…
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Clinical SAS/SDTM Programmers Katalyst HLS - Job Responsibilities: Develop and validate SAS ® programs to produce high-quality deliverables within set timelines in accordance with company and regulatory requirements. The deliverables include SDTM and ADaM datasets, tables, listings and figures. Review and provide feedback on deliverables from other clinical groups, including but not limited to statistical analysis plans; table, listing, and figure shells; data management plans; data transfer plans; Safety Report Specification; electronic data entry screens; and case report forms. Clear and proactive communication with Study and Project teams to clarify requirements and specifications, update on assignment status and convey data irregularities. Create and validate global macros or systems that streamline repetitive operations to increase programming efficiency. Ensure the edit check specification and data quality for ongoing clinical study. Keep abreast of SAS enhancements and supports achievement of major reporting delivera
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