Myles Laney’s Post

Are you looking for ways to reduce your clinical operations cost? Under the current financial tightening conditions, we understand the need to maximize returns. ClinFocus boasts experienced teams across 4 continents, utilizing cutting-edge technology-driven processes to guarantee precision, elevate data quality, and significantly reduce costs.     Our services that speak excellence includes:    EDC Development (Medidata Rave Accredited)  Clinical SAS Programming  Clinical Data Management  Biostatistics  Centralized Data Analytics  Medical and Safety Review  Site management and Clinical Operations Support     Let's discuss why working with ClinFocus should be on your 2024 agenda! 📆 Drop a comment or shoot us a direct message info@clinfocus.com.    #CostSavingClinicalResearch #BiometricsServices #DataQuality #ClinicalTrials2024 #ClinFocusAdvantage 

"Excited to kickstart my career in Clinical Data Management, Clinical Research, Clinical SAS, and Regulatory Affairs! 🚀 As a recent graduate, I'm eager to apply my skills and passion to make an impact in these fields. Open to opportunities and ready to learn and grow. Let's connect and explore how I can contribute to your team! #FreshGrad #ClinicalDataManagement #ClinicalResearch #ClinicalSAS #RegulatoryAffairs #NewBeginnings"

I am looking new opportunity. I have Over 3.9 years of experience in Clinical Data Management (Lab Data), Clinical Data Programming, Data Validation, Data mining, Data Transfer, etc. Currently associated with Labcorp as an Associate Programmer. Experienced in managing Lab Data, from multiple therapeutic areas. Demonstrated skills in programming data files within the SQL database in multiple formats (CSV, XML, TXT SAS7BDAT, XPT). #SAS #Clinical #clinicaltrail #cro #Clinicalsasprogramming #dataanylyst #experienced #pharmaceutical #career #dataanylyst

Thanks all for the overwhelmed response to OptivalueTek's Webinar on 🌹 "Clinical Trials Landscape for Programmers" 🌹 . The webinar was intended to help programmers to know about the Clinical Trials domain. Some of the topics covered like 💊 Drug Discovery, Pre-Clinical, Clinical Introduction to Protocol and its contents, Typical roles such as Sponsors, Contract Research Organization, Vendors, Investigator, Clinical Coordinator, Clinical Monitor, Data Manager or Data Scientist, Clinical Database programmer, Biostatistician, Clinical Coder, Medical Writer, Clinical Analyst and expert, Marketing and Supply Chain, Post Marketing studies, Emerging Trends such as Decentralized clinical Trials, Including Real World evidence data in Clinical Trials. 💊 Based on our attendees demand, we will thrive to schedule follow-up webinars in the coming months. Thanks once again for your extended support Our skill development programs are designed to enable young talents free of cost #webinar #clinicaltrials #clinicalresearch #statisticalprogrammer OptiValueTek

IQVIA is hiring for Sr. Biostatistician for Bangalore. Job Description: Job Overview Develop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysis files, tables, and figures. Communicate with clients regarding study protocol or statistical analysis issues as they arise. Communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results. Interpret analyses and write statistical sections of study reports. Accountable for controlling costs and maximizing revenue recognition. Provide training, guidance and mentorship to lower level and new staff. Essential Functions • Production of High-Quality Deliverables: Completes and reviews more complex assigned tasks with a focus on accuracy. Conducts all appropriate validation requirements, according to Standard Operating Procedures (SOPs), for each task undertaken. Checks programming logs for cleanliness and correct processing of data. Inputs into Data Issues log and follows issues to appropriate resolution. • Leadership: Perform statistical team lead role on single studies. Through this, works closely with the Project Team Lead and supervisor to deliver on time, with high quality and within budget. Build and maintain effective customer relationships, driving statistical discussions, providing support and/or guidance for statistical activities. Demonstrates and promotes efficient communication. If in lead role, runs meetings, documenting where necessary and following up on actions. Actively participates in internal project team meetings, provides timely progress updates. As a lead, will have input on estimate at completion (EAC) reporting. • Data Management: Assist in reviewing or advising data management staff on database design, validation checks and critical data. Handles data issue resolutions. If in lead biostatistical role, handles lock and unblinding process with appropriate supervision. • Statistical Analysis Plan (SAP) and Shells: Authors or performs quality control review (QC) of SAPs and shells. Make best use of resources and expertise within the organization (e.g. Libraries, templates and consultants for complex statistical methods). May author or QC complex SAPs, under supervision if needed. • Datasets: Writes and maintains programming specifications. Programs assigned datasets to industry standards. Handles dataset derivations and assignment. • Tables, Listings and Figures (TLFs): Writes programming specifications for statistical analyses outputs. Programs TLFs, maximizes programming efficiency with use of tools, where applicable. Checks resulting output for format and content, and questions specification as needed. Ensures consistency across items produced. • Timelines: Plans and documents timelines, forecasts resource needs, suggests work may be out of scope. #biostat #statisticians #hiringpost #iqvia

The future of clinical research careers looks promising with increased demand for professionals due to more clinical trials and new treatments. Emerging roles like Clinical Data Scientist and Decentralized Clinical Trial Coordinator, along with remote work opportunities, are on the rise. Key skills in data analysis, regulatory knowledge, and familiarity with EDC systems, AI, and ML are highly valued. Salaries range from $45,000 to $150,000 annually depending on the role and experience. Advancing your career involves continuous learning, networking, specializing in high-demand fields, and obtaining certifications. Staying updated and embracing technological advancements are essential for success. #ClinicalResearch #PharmaJobs #ClinicalTrials #DataScience #RemoteWork #JobGrowth #CareerAdvancement #SkillsDevelopment #RegulatoryKnowledge #HealthcareInnovation #ClinicalData #MedicalResearch #BiotechCareers #HealthInformatics #ProjectManagement #Certifications #PharmaIndustry #SalaryGrowth #TechInPharma #ContinuousLearning

Career opportunity in a reputed Pharmaceutical Organization for the role of Biostatistician. Interested candidates can share their updates CVs on hire@biojobz.com. Role: Biostatistician Experience: 4+ Years Location: Gurugram (Hybrid) Role & Responsibilities (Not limited to):  Protocols: Direct development of statistical designs and analysis procedures for scientific protocols, ensuring they are scientifically sound, aligned with project strategy, meet regulatory objectives, and make optimal use of the data to be collected. Ensure statistical analysis plan is methodologically sound and consistent with objectives of the protocol. Assist in developing project and functional standards of data collection and analysis, and implement these standards.  Database Activities: Collaborate with data sciences, statistical programming, and other stakeholders to ensure data collection instruments and database implementation meets short and long-term project needs. Contribute to data monitoring plans. Develop and implement project specific data standards. Ensure accuracy and consistency of data released for statistical analysis.  Statistical Analyses: Demonstrate extensive understanding of statistical concepts and methodology. Propose novel statistical methodological approaches leading to improvement in the efficiency and sensitivity of study results. Provide sufficient details to allow programming implementation. Ensure that all statistical analyses specified in scientific protocols and analysis plans are conducted appropriately. Determine need for development of novel statistical methodology.  Reports and Publications: Ensure that study results and conclusions are scientifically sound, clearly presented, and supported by statistical analysis. Prepare oral and written reports to communicate results. Represent data and statistical sciences on project issues at management review and project team meetings. Provide in-depth statistical review for scientific reports and publications. Ensure the accuracy of the statistical component of scientific reports and publications and high quality.  Project team involvement: Partner with clinical and regulatory to create development strategies for assigned project. Represent department on project team(s) to provide statistical input to compound/drug development and align with functional management. Lead communication between assigned project team(s) and department to ensure timely communication of project team updates, proper statistical strategies, and alignment of decisions/priorities between the project team and functional management. #Biostatistics #Biostatistician #Clinalcaltrails #Biostats #Statisticalmanager #Statistician #SAS #Clinicalphases #Statisticalprogrammer #Statisticalprogramming

🌟 Pursuing Director/Executive Roles in Biotechnology Research! 🌟 Hello LinkedIn community, I'm thrilled to share that I am actively pursuing director and executive level opportunities in the dynamic field of biotechnology research. With a rich background encompassing data analysis, expert SAS programming, and CDISC SDTM and CDISC ADaM expertise, I bring a holistic approach to decision-making. However, what truly sets me apart is my extensive management and operational experience. As a seasoned professional, I've successfully led cross-functional teams, overseen projects from conception to execution, and consistently delivered results that align with strategic objectives. My time in the Air Force, where I specialized in finance and accounting, has honed my ability to manage resources efficiently and execute with precision. These skills, coupled with my biostatistics proficiency, position me to drive transformative initiatives within the biotechnology research landscape. I'm excited about the potential to make a significant impact and drive growth within an organization. If you have insights into director or executive roles or would like to connect, I invite you to reach out. Let's explore how my comprehensive skill set and background can contribute to your organization's success. Thank you for your time and consideration! #BiotechnologyResearch #PeopleManagement #OperationalLeadership #SAS #CDISC #SDTM #ADaM #Biostatistics #ClinicalTrials #RWE #CRO6MoNonCompete #USARemoteOnly #Unicorn

Opportunity

Clinical SAS Programmer - Irving, TX Katalyst HealthCares & Life Sciences Overview: Clinical trial objectives, design, endpoints, and procedures defined in Protocol and Statistical Analysis Plan (#SAP). Develop programs that convert raw #SAS datasets into standard format and improve existing programs by creating standard programs and macros. #CDISC guidelines required for regulatory submissions. Independently program #CDSIC #ADaM / #ADS datasets and Tables Listings and figures (#TLFs) as per requirement of study including efficacy related outputs. Provide validation support to create #ADS or #SDTM+, #SDTM and #ADaM datasets and #TLFs & documentation as per the specifications within set timelines Good Clinical Practice (#GCP) and International Conference on Harmonization (#ICH) guidelines .Create #ADS / #ADAM datasets from #RAW / #SDTM datasets according to project / #CDISC analysis data model standards; Independently write, test, run. Reach me @908-373-5281 ll veer@katalysthls.com #CDSIC #ADaM #ADS #SDTM #SAP #w2 #USA #ADS #CDISC #Genetherpeutics #Rprogramming #SASMacros, #SAS #STAT, #SAS #Graph, #SAS #SQL #SAS #ODS.#USA #W2 #Statistics, #Mathematics #Biotechnology #Pharmaceutical You can Apply Here:https://shorturl.at/eijEQ