4 Therapeutic Jobs

Role & responsibilities Assess patients nutritional needs by evaluating their medical history, current health condition, and dietary requirements. Develop personalized meal plans based on patient's specific needs, taking into account any dietary restrictions or medical conditions. Educate patients and their families on proper nutrition and the importance of a healthy diet to aid in their recovery or manage their condition. Monitor patients progress and adjust their meal plans as necessary, collaborating with the healthcare team to ensure optimal patient outcomes. Provide guidance and support to patients with special dietary needs, according to their medical and nutritional status. Document patients nutritional assessments, interventions, and progress in their medical records to ensure accurate and comprehensive patient care. Collaborate with kitchen staff and food service providers to ensure that meals meet patients dietary requirements and preferences. Participate in multidisciplinary team meetings to contribute expertise and provide input on patients nutritional needs and treatment plans. Conduct and attend nutrition-related workshops, seminars, and educational programs for healthcare professionals, patients, and the community. Preferred candidate profile Education : M.Sc. in Dietetics and Nutrition (Must) Minimum 2 years of Exp.

Hi, Wishes. Pleasure connecting with you. Job Summary: We are hiring mid-level Statistical Programmers (4 - 8 years of experience) with strong hands-on expertise in SAS programming for clinical trials. The role requires experience in SDTM and ADaM dataset creation, TLF programming, and knowledge of CDISC standards. You will be working on end-to-end programming activities for Phase IIV clinical studies. Mode of Work : WFO Exp Range : 4 to 8 yrs Work Location : CHENNAI CTC Range : Best in the industry ***** Looking for SHORT JOINERs ***** Key Responsibilities: SDTM Programming: Create and validate SDTM datasets as per CDISC guidelines. Perform CRF annotation and author/review specifications . Generate Define.xml and ensure compliance using Pinnacle 21 . Work on Study Data Reviewers Guide (SDRG) and submission packages. ADaM Programming: Develop ADaM datasets for Safety and Efficacy analysis. Write and validate ADaM specifications and ensure alignment with SAP. Prepare ADaM Define.xml and reviewer documentation. TLF Programming: Generate and QC Tables, Listings, and Figures (TLFs) as per SAP. Use SAS Graph and macros to build clinical outputs. General Programming & Project Work: Independently write or modify SAS programs from scratch or using templates. Develop or enhance custom macros to streamline programming tasks. Work in both production and validation programming roles. Handle multiple studies simultaneously , ensuring high-quality deliverables. Participate in integration and pooling (ISS/ISE) of datasets. Work on CRT packages and electronic submission readiness. Required Skills: Strong knowledge of SAS Base, SAS/STAT, SAS/GRAPH in a clinical trial setting. Solid understanding of CDISC SDTM and ADaM standards . Experience with Define.xml creation and validation tools like Pinnacle 21 . Hands-on exposure to multiple therapeutic areas and clinical phases . Experience in ISS/ISE and integrated datasets is a strong plus. Nice to Have: Familiarity with tools such as Define.xml Generator, SAS Clinical Standards Toolkit . Knowledge or EXP in R Programming is OPTIONAL Exposure to MACRO programming and reusable code frameworks . Understanding of regulatory requirements for FDA/EMA submissions . What We Offer: Projects with top global pharma clients. Work with a high-performing and collaborative clinical data team. Competitive compensation, learning, and growth opportunities. If Interested, click APPLY ONLINE for IMMEDIATE response. Best, ANANTH | GSN HR | 9840035825 | Google review : https://g.co/kgs/UAsF9W

KEY TASKS & RESPONSIBILITIES Determine resourcing needs per project load, deadline requirements and resource utilization Create or review and approve programming plans at study and project level Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plans, SAPs, etc.) Responsible for developing and maintaining programming and validation specifications for TLGs as per requirements provided by the Biostatistician Create and maintain SAS programs to produce outputs to support the analysis and reporting of clinical trials Assist Biostatisticians by suggesting algorithms to address novel analysis requests Develop analysis datasets for trial level reporting and integrated safety and efficacy activities Program and QC data listings, summaries and Graphs as defined in SAP Develop re-usable utility macros to build a macro library to support programming tables, listing and graphs for all phases of clinical trial reporting Create submission ready SDTM and ADaM datasets following standard industry processes Performs peer review of all SAS Programmers deliverables Serve as Subject Matter Expert for Statistical deliverables and lead task forces to develop complex, technical solutions for projects or business needs Collaborate with the project team and other Professional Services Managers to ensure the deliverables are completed on time with high quality Develops and maintains good working relationships with internal cross functional teams and Clients Develops, revises, and maintains Standard Operating Procedures and Work Instructions. Assists in the training of Standard Operating Procedures and Work Instructions. Maintain all project documentation as required by SOP and Processes Ensure compliance with eClinical Solutions and industry quality standards, guidelines, and procedures May serve as Lead Statistical Programmer on projects when needed Other duties as assigned

KEY TASKS & RESPONSIBILITIES Determine resourcing needs per project load, deadline requirements and resource utilization Create or review and approve programming plans at study and project level Provide input on key study-related documents produced by other functions (e.g. CRFs, Data Management Plans, SAPs, etc.) Responsible for developing and maintaining programming and validation specifications for TLGs as per requirements provided by the Biostatistician Create and maintain SAS programs to produce outputs to support the analysis and reporting of clinical trials Assist Biostatisticians by suggesting algorithms to address novel analysis requests Develop analysis datasets for trial level reporting and integrated safety and efficacy activities Program and QC data listings, summaries and Graphs as defined in SAP Develop re-usable utility macros to build a macro library to support programming tables, listing and graphs for all phases of clinical trial reporting Create submission ready SDTM and ADaM datasets following standard industry processes Performs peer review of all SAS Programmers deliverables Serve as Subject Matter Expert for Statistical deliverables and lead task forces to develop complex, technical solutions for projects or business needs Collaborate with the project team and other Professional Services Managers to ensure the deliverables are completed on time with high quality Develops and maintains good working relationships with internal cross functional teams and Clients Develops, revises, and maintains Standard Operating Procedures and Work Instructions. Assists in the training of Standard Operating Procedures and Work Instructions. Maintain all project documentation as required by SOP and Processes Ensure compliance with eClinical Solutions and industry quality standards, guidelines, and procedures May serve as Lead Statistical Programmer on projects when needed Other duties as assigned