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The purpose of this role is to understand the client requirements and develop business objects, with the aim to provide solutions to client specifications and support to resolve complex issues Responsibilities Develop and implement reports and dashboards using Business Objects Webi Intelligence, Crystal Reports and Xcelsius. Understand reporting database schemamodel, identify joinstables, and perfo

Overview: We have an exiting opportunity for Clinical Data Manager I to lead, coordinate and action all tasks relating to Clinical Data Management from the start to the finish of a study and to project manage studies across DM functions. Responsibilities: Core Accountabilities Activities required of a Clinical Data Manager I however not restricted to are as below: Project management for allocate

Key Responsibilities: Reviews the Data Management Plan and associated documents and provides relevant inputs to the checks, listings, cleaning plan etc. Adheres to the requirements of studyspecific Clinical Data Management Plans for assigned projects by reviewing & processing clinical trial data to ensure the accuracy & consistency of clinical databases Write and executes the validation plan of che

Should have study start up exp, develop test cases. Exp: 2.64 yrs of relevant exp in CDM with RAVE At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible

Review Study protocol and Case Report Forms. Prepare the CRF standards for all phase of studies. Preparation and review of DVS Data Validation specification. Preparation and review of manual listings for the study. Preparation and review of eCRF Completion guidelines for the study. Preparation and review of Time and Event schedule for the study. Creation and review of UAT User Acceptance Testing. P

Under the guidance of Level I & II Clinical Dietitian Coordinate all phases of nutrition care including Nutrition assessment Nutrition care planning Nutrition monitoring Nutrition education and counseling of hospitalized patients Perform duties in support of and in compliance with performance improvement plans, JCI, and other licensing, accrediting, and regulatory agencies. Provide nutrition servic

Conduct daily ward rounds for details of Anthropometry, diet history, diagnosis, and then prescribe the diet after consulting with the concerned Doctor. Ensure that the prescribed diet is supplied to the patients. Counsel the in patients at the time of discharge.REQUIRED SKILLS AND EDUCATION: Candidates must have PG degree in Msc Food and Nutrition Applied Nutrition Nutrition and Dietetics. Cand

Responsibilities Assessing patients healthDiscussing eating habits with the patientProviding educational resourcesAdjusting diet plans as per needsTracking the progress of patientsJob

Job Overview: Job Location: Bangalore; Contract Position for 6 months ? Follow applicable departmental Standard Operating Procedures and Work Instructions. ? Complete required trainings according to required timelines. ? Complete daytoday tasks ensuring quality and productivity. ? Maintain project and technical documentation in an appropriate manner. ? Perform checks to ensure quality of work comp

Overview: We have an exiting opportunity for Clinical Data Manager I to lead, coordinate and action all tasks relating to Clinical Data Management from the start to the finish of a study and to project manage studies across DM functions. Responsibilities: Core Accountabilities Activities required of a Clinical Data Manager I however not restricted to are as below: Project management for allocate

Overview: We have an exiting opportunity for Clinical Data Manager I to lead, coordinate and action all tasks relating to Clinical Data Management from the start to the finish of a study and to project manage studies across DM functions. Responsibilities: Core Accountabilities Activities required of a Clinical Data Manager I however not restricted to are as below: Project management for allocate

Identify and select routine cases for processing, determining appropriate prioritization criteria, and noting reasons for any delays. Assess cases to distinguish those with particular complexities andor specific issues, and escalate appropriately. Review, rank, verify, process and document: event terms; case classifications validity, seriousness, expectednesslistednesslabelledness; special scenari

Job Title : Clinical Admin Coord Senior Educational Qualifications 10th and Above Work Experience Minimum 1 Year Experience in International Contact Center Technical Skills & Competencies Must have Good to have Typing speed, beginner level, Command over language Experience in working with US clients Neutral accent Able to work in night shifts Be able to multi task Good conversational

B.Sc.Nursing is the prerequisite qualification.A good communication skill in English is a must.Effective Interpersonal relations & caring attitude.34 years in Clinical ExperienceAssess patient condition by monitoring vital signsRecords patient information by making entries in the patient journalReviewing patient care journalKeeping family informed.Maintains continuity of patient home care by docume

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our 39,000 employees around the world work to discover and bring lifechanging medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism.

Education Requirements: Minimum Bachelor's degree in Computer Science, Engineering, Statistics, Technical Science or related field with 35 years of clinical experience in a pharmaceutical, biotech, CRO, or Regulatory agency. Mandatory Skills Required: Creates reporting and analytics solutions with appropriate oversight that support the quality and timely delivery of clinical data reports and visua

Education Requirements: Minimum Bachelor's degree in Computer Science, Engineering, Statistics, Technical Science or related field with 35 years of clinical experience in a pharmaceutical, biotech, CRO, or Regulatory agency. Mandatory Skills Required: Creates reporting and analytics solutions with appropriate oversight that support the quality and timely delivery of clinical data reports and visua

Qualifications A graduate degree or Post Graduate degreediploma preference in Health Science, Science, or Clinical is required.Good organizational, communication and computer skills required.Ability to exercise excellent attention to detail required.Ability to act independently and with initiative required to resolving problems.Medical terminology exposure preferred.Knowledge of operating procedure

Job Specification Purpose: To action all tasks relating to Clinical Data Management from the start to the finish of a study. To support Project Manager in studies across DM functions. Core Accountabilities: Activities required of a Clinical Data Coordinator I however not restricted to are as below: To assist in the testing of databases prior to activation. To assist in the preparation of study sp

Overview: An exciting opportunity has arisen for a Clinical Data Coordinator within our Clinical Research Organisation CRO, Quanticate. Responsibilities: Job Specification Purpose: To action all tasks relating to Clinical Data Management from the start to the finish of a study. To support Project Manager in studies across DM functions. Core Accountabilities: Activities required of a Clinical Da

Job Overview: Job Location: Bangalore; Contract Position for 6 months ? Follow applicable departmental Standard Operating Procedures and Work Instructions. ? Complete required trainings according to required timelines. ? Complete daytoday tasks ensuring quality and productivity. ? Maintain project and technical documentation in an appropriate manner. ? Perform checks to ensure quality of work comp

JOB DESCRIPTION: Requirement & Qualification: Post Graduate degree in Pharmacy ChemistryQuality ControlPharmacokinetics or MSc Chemistry 1st Class Academic Record from a reputed college, with a Diploma in Clinical trials. The candidate should have strong quantitative and analytical skills. Heshe should have strong written and oral communication skills, with exposure to or basic understanding of cl

About Novotech: Novotech is internationally recognized as the leading independent and fullservice contract research organization CRO in the Asia Pacific region. We provide a wide range of clinical development services across all research phases and therapeutic areas; and have been instrumental in the success of hundreds of Phase I IV clinical trials throughout the Asia Pacific. Powered by the hi

Ensures quality of the clinical monitoring and site management deliverables within a project and maintain proper visibility of its progress by the use of approved systems and or tracking tools. May include the development of the Clinical Management Plan CMPSite Management Plan SMP.Interacts with the client and other functional departments related to clinical monitoring and site management activiti

About Novotech Novotech is internationally recognized as the leading independent and fullservice contract research organization CRO in the Asia Pacific region. We provide a wide range clinical development services across all research phases and therapeutic areas and have been instrumental in the success of hundreds of Phase I IV clinical trials throughout the Asia Pacific. Our people are one of o

ABOUT THIS COMPANY Indegene is a leading provider of R&D, commercial and marketing solutions to global pharmaceutical and healthcare organizations. We partner with clients to drive both productivity and revenues by delivering better patient outcomes, optimizing cost, enhancing R&D agility, and improving sales and marketing effectiveness. We apply deep scientific knowledge, flexible delivery models

]Job Description The main objective of this role is to efficiently lead Project Team activities and actively participate in the planning and implementation of consistent Clinical Trial processes. You will: Coordinate and supervise Project Teams in APAC Monitor, collect and report project timelines, milestones, enrollment and general status for updates Direct communication with Global Project Mana

Job Description The main objective of this role is to efficiently lead Project Team activities and actively participate in the planning and implementation of consistent Clinical Trial processes. You will: Coordinate and supervise Project Teams in APAC Monitor, collect and report project timelines, milestones, enrollment and general status for updates Direct communication with Global Project Manag

PURPOSE The Data Engineer role manages the flow of information. Designs, builds and maintains the databases. Establishes the maintenance of appropriate data backups and the ability to recover to any point within that backup. Provides database technical services and support to both internal and external customers. COMPETENCIES & SKILLS Assists in managing the life cycle of multiple database tools b

JOB DESCRIPTION You will participate in the creation of study specific coding conventions and perform coding of medical terminology. Your responsibilities will include review of coding, raising coding queries and updating the clinical database as required. You will also provide support to other members of the coding group. You will be skilled in general data management activities with a sound know

JOB DESCRIPTION You will participate in the creation of study specific coding conventions and perform coding of medical terminology. Your responsibilities will include review of coding, raising coding queries and updating the clinical database as required. You will also provide support to other members of the coding group. You will be skilled in general data management activities with a sound know

EducationExperience: Master?s or bachelor?s degree in pharmacyLife Sciences with minimum 13 years of delivering end user training experience with at least one clinical application CTMS, eTMF or Safety database in a CROPharma company. 58 years of progressive clinical research experience. Responsibilities Ownership Serves as the primary trainer for clinical systems and deliver end user training o

Job Title : Clinical Statistical Programmer Job location : Chennai Bangalore Home based Office based No of years of experience: 3+ years of relevant exp in SDTM domain and SAS Skills Education Qualification: Any graduation Salary : As per Industry standards with attractive benefits Skill set : Strong knowledge of SAS programming language, Define.xml, SDTM aCRF, cSDRGs Job Functions: Responsible fo

A post graduate degree MD, DNB in these subjects is not mandatory. Fresh MBBS graduates may also apply.The physician is required to have a scientific temper and excellent communication written and verbal skills in English. The job will entail working on varied assignments straddling translational medicine, clinical development and drug safety. The candidate will play a role in the execution functi

Job Overview: Global Specimen Solutions GSS is wholly owned company of Covance Inc., providing specialty services in the holistic specimen tracking space. GSS improves translational science through industry best practices and a uniquely powerful pipeline data management analytics solution. GSS reduces the time, cost and risk of specimen based research, while building robust, healthy data pipelines

Job Overview: Global Specimen Solutions GSS is wholly owned company of Covance Inc., providing specialty services in the holistic specimen tracking space. GSS improves translational science through industry best practices and a uniquely powerful pipeline data management analytics solution. GSS reduces the time, cost and risk of specimen based research, while building robust, healthy data pipelines

Job Overview: Global Specimen Solutions GSS is wholly owned company of Covance Inc., providing specialty services in the holistic specimen tracking space. GSS improves translational science through industry best practices and a uniquely powerful pipeline data management analytics solution. GSS reduces the time, cost and risk of specimen based research, while building robust, healthy data pipelines

Requirement & Qualification: Post Graduate degree in Pharmacy ChemistryQuality ControlPharmacokinetics or MSc Chemistry 1st Class Academic Record from a reputed college, with a Diploma in Clinical trials. The candidate should have strong quantitative and analytical skills. Heshe should have strong written and oral communication skills, with exposure to or basic understanding of clinical trials. Lo

Job Summary Responsible for study management and execution of studies as per the established Standard Operating Procedures SOP, Good Clinical Practices GCP, Good Laboratory Practices GLP best practices and regulatory requirements Job Responsibilities Conducts duties following established Apotex Research Pvt. Ltd., Bioequivalence Center?s Standard Operating Procedures and in a manner consistent wit

Job Description : QUALIFICATION: Any Graduation Full Time 2+ years of equivalent work experience in Vendor Management, Supply Chain, Inventory Management and Order Management. Experience in retail industry, MIS reporting Experience in fulfilment, demand planning & supply chain Experience in managing multiple product vendors and categories Excellent written and verbal communication skills. Effectiv

writing drug trial methodologies proceduresidentifying and briefing appropriate trial investigators cliniciansproviding clinicians with instructions on how to conduct the trialscollecting and authenticating data collection forms commonly known as case report formsmonitoring progress throughout the duration of the trialwriting reportsJob

Brief Description about the Project: The CRTP fellows will undergo rigorous training in every aspect of clinical research as well as detailed training in epidemiology and biostatistics. The fellow with specialization in Paediatrics will be mentored for indepth research program on protein accretion during early infancy while the fellow with specialization in Community Medicine will learn innovative

Job Overview: Job Location: Bangalore; Contract Position for 6 months ? Follow applicable departmental Standard Operating Procedures and Work Instructions. ? Complete required trainings according to required timelines. ? Complete daytoday tasks ensuring quality and productivity. ? Maintain project and technical documentation in an appropriate manner. ? Perform checks to ensure quality of work comp

Job Overview Provide advanced technical expertise to develop and maintain programs to meet internal and external clients? needs. Plan and lead the development of projectrelated solutions to the full scope of statistical programming tasks. Provide technical expertise to the Statistical Programming department. Essential Functions Perform and plan: i the programming, testing, and documentation of prog

Basic qualifications: MSc in a statistical discipline Statistics, Biostatistics or related. Experience 2 yrs + preferable in the design, execution, analysis and interpretation of clinical trials. Expertise in a broad range of statistical methodologies. Excellent interpersonal and communication skills; record of building and maintaining strong working relationships; demonstrated ability to explain

Job Description About Accenture: Accenture is a leading global professional services company, providing a broad range of services in strategy and consulting, interactive, technology and operations, with digital capabilities across all of these services. We combine unmatched experience and specialized capabilities across more than 40 industries ? powered by the world?s largest network of Advanced Te

Job Description About Accenture: Accenture is a leading global professional services company, providing a broad range of services in strategy and consulting, interactive, technology and operations, with digital capabilities across all of these services. We combine unmatched experience and specialized capabilities across more than 40 industries ? powered by the world?s largest network of Advanced Te

Job Description : Minimum 5 years of experience with SAS programming for clinical trial data. Generate data sets, tables, listings, and figure outputs Establish standardized programming procedures and work instructions. Technical Requirements for SAS Programmer Work directly with the ClientClient to establish timelines and assign tasks. Strong background working in a CRO or Pharmaceutical envi

Job Description : Minimum 5 years of experience with SAS programming for clinical trial data. Generate data sets, tables, listings, and figure outputs Establish standardized programming procedures and work instructions. Technical Requirements for SAS Programmer Work directly with the ClientClient to establish timelines and assign tasks. Strong background working in a CRO or Pharmaceutical envi