Internship Content Writing #freshersjobs #helpinghand #Engineeringjobs #jobs #itjobs #hrjobs #fresher #opportunities #intern #recruitment #engineeringjobs #recruiting #vacancy #engineer #recruitment #jobs # #fresher #hiring #employment #experience #data #jobseekers #collegestudents #internship This is a full time (3 months) Internship offer for following positions: - (1) Content Writing

*NEW NEW NEW PROJECT

Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights into outcomes to address modern market realities. Our Clinical Development model brings the customer and the patient to the center of everything that we do. We are continuously looking for ways to simplif

Mankind Pharma Recruitment 2023 Job Title: Quality Control Coordinator Company: Mankind Location: Bangalore, Bellandur Job Summary: Mankind is currently seeking a Quality Control Coordinator to join our team in Bangalore, Bellandur. As a Quality Control Coordinator, you will play a vital role in ensuring the quality and compliance of our products and processes. You will be responsible f

Project Role: Python PySpark Developer Work Experience: 4 to7 Years Work location: Bengaluru Work Mode: Hybrid Must Have Skills: Python, PySpark Good to have Skills: Azure, Azure Databricks, PostgreSQL, Clinical Data Essential Functions: • Works collaboratively with architects and testers across regions. • Reviews business requirements with regards to reporting, advises on the p

Requirement: knowledge in Anatomy and Physiology Good communication and interpersonal skills Basic Computer Skills

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Clinical Research Associate #clinicalresearch #clinicaltrials #clinicaldataanalyst #REGULATORYaffairs #medicalcoding #medicalbilling #research #healthcare #medicalresearch #clinicaltrial #science #clinical #health #clinicalstudies #pharma #medical #pharmacy #biotech #clinicareers #pharmacovigilance #pharmaceuticals #clinicalstudy #pharmacovigilance #medicalaffairs #clinicalresearchassociate #ph

Ensuring that the IST investigator is providing study updates in tool as applicable to the customer viz. regulatory updates, enrolment data, confirming that safety information is being transferred to customer as required, notification of any amendments to either the protocol or informed consent. Reviewing that the agreed upon contractual milestones are being met and raising to customer for any thre

Full Job DescriptionRole Purpose: We are looking for a Key Contributor who will help us drive Sales Efficiency across AMESA region. This includes ownership of revenue roadmap forecasting, support to the regional leaders on all aspects of commercial operations and insights, reporting, management of Business Development incentive plans, annual planning etc. Works closely with sales, commercial and f

Undertakes primary medical review of cases, including medical assessment of the case for seriousness, listedness/labeling, causality, adverse event coding and narrative review. Updates and documents daily case data, case-feedback in appropriate trackers/tools to facilitate tracking and workflow management Assumes complete responsibility for all assigned deliverables in line with expected quality,

Individual has responsibility for coordinating the activities of routine and non routine studies in compliance with appropriate company standards, GLP, GCP, GMP and regulatory guidelines specified in the study plans, protocols, or work agreements governing the work in which they are involved in a timely, efficient and quality manner. Responsibilities/Duties Individual Contributor B. People Respo

Assist with review of clinical trial data in accordance with Data Management Plans and/or Data Review Guidelines and raise queries to resolve erroneous, missing, incomplete data. Demonstrates capability to read and follow study timelines for on-time deliverables and potential to assist with inputs on study design or capable to make suggestions to study timelines when warranted. Run and execute addi

Management of projects under direction of a Project Manager / Director as assigned. Ensure site monitoring responsibility for clinical studies are conducted according to Standard Operating Procedures, ICH Guidelines and GCP. Work Closely with project teams in implementation of best TRR practices & applicable project plans as assigned (Implementation of Initiatives either independently or with t

Ensuring that the IST investigator is providing study updates in tool as applicable to the customer viz. regulatory updates, enrolment data, confirming that safety information is being transferred to customer as required, notification of any amendments to either the protocol or informed consent. Reviewing that the agreed upon contractual milestones are being met and raising to customer for any thre

Labcorp is proud to be an Equal Opportunity Employer: As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status. For more information about how we collect and store your personal data, please see our Privacy Statement.

Performs review of clinical monitoring visit reports for allocated projects ensuring consistency across protocols and/or regions and escalates any protocol, site, and/or CRA issues or trends noted during the report review process to CTM. Liaises with clinical monitoring staff for prompt trip report review submission and approval as per the stipulated timelines of PPD and/or the Sponsor. Plays an

JOB DESCRIPTION Provides administrative and technical support to the Project Team. Supports audit readiness by ensuring files are reviewed on schedule detailed in in the organization's WPD and department guidance document. Supports training of new staff and participates in departmental initiatives to support process improvements/enhancements. According to the specific role Central or Local, co

JOB DESCRIPTION We are vital links between an idea for a new medicine and the people who need it. We are the people of PPD — thousands of employees in locations worldwide connected by tenacity and passion for our purpose: to improve health. You will be joining a truly collaborative and winning culture as we strive to bend the time and cost curve of delivering life-saving therapies to patients. Our

Ensuring that the IST investigator is providing study updates in tool as applicable to the customer viz. regulatory updates, enrolment data, confirming that safety information is being transferred to customer as required, notification of any amendments to either the protocol or informed consent. Reviewing that the agreed upon contractual milestones are being met and raising to customer for any thre

Full Job DescriptionJob Overview Under close guidance, translates and verifies data from various sources such as prescriber information and product information. Essential Functions Analyzes and translates 3rd party prescriber data to IQVIA master file conventions.Resolves "unknown" entries by researching through internal references such as phone number reference tool or through external research b

Full Job DescriptionJob Overview Responsible for the on-time completion of projects or components of large, complex projects for clients in the life sciences field. Identifies and elevates potential new business opportunities and assists in the sales process. Essential Functions Participates or leads teams in the design, development and delivery of consulting projects or components of larger, comp

Full Job DescriptionJob Description for PostgreSQL Database Administrator Full time database engineer, working as both development and Production Postgres DBA. The database engineer role seeks to maximize uptime and performance of databases, utilize query proxies, connection caches, and other technologies as needed to produce clean interfaces to work with (and protect) data, account management, ba

Full Job DescriptionPerform and plan: (i) the programming, testing, and documentation of programs for use in creating statistical tables, figures and listing, (ii) the programming of analysis dataset (derived datasets) and transfer files for internal and external clients. and (iii) the programming quality control checks for the source data and report the data issues periodically. Detect errors in d

Full Job DescriptionInformed Consent Form Specialist Job Description As an ICF Specialist you will be a part of Country Site Activation (CSA) Global Services Team and perform tasks at a global level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary

Full Job DescriptionTalent Acquisition Specialist Are you looking to be part of a multinational and fast-paced environment with a great team of people ? If so, this is your OPPORTUNITY! What are our expectations? Support the continuous improvement of the staffing function through development and implementation for all staffing programs in an assigned business unit/department, primarily in one geo

Full Job DescriptionJob Overview Provide comprehensive data management expertise to Clinical Data Management (CDM) to provide efficient, quality data management products that meet customer needs. Provide leadership either in the role of the Data Operations Coordinator (DOC), the role of the Data Team Lead (DTL) or in a leadership role in a specific CDM task (e.g., lead of a task on a megatrial, cod

Full Job DescriptionUnder guidance from management, define and maintain departmental standards, SOPs and working practices; and lead process improvement initiatives.Develop training materials and execute training in Statistical Programming activities, for new and existing staff.Make presentations to clients and other interested individuals about the processes and procedures of the Clinical Reportin

Full Job DescriptionMain Responsibilities: Requirements Gathering and analysis by driving/contributing to the requirements workshops Facilitate/contribute to client demo sessions/workshops Performs extensive testing of the application/custom code to identify/fix all issues during the testing phase Authoring and execution of validation documents like Test scenarios, Operational and Performance Quali

Full Job DescriptionJob Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions Under general supervision, serve as Single Point of Contac

Full Job DescriptionJob Overview Provides high quality, on-time input to client projects in the life sciences field. Assignments typically require analysis and problem solving within an established framework. Essential Functions Under direct supervision, assists with the review and analysis of client requirements or problems and assists in the development of client solutions.Assists in the develop

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Data Analytics Associate #datasciencetraining #dataviz #tableau #excel #programmer #coder #datascientists #analyst #machinelearningalgorithms #powerbi #digitalmarketing #datascienceeducation #datastructure #ml #dataentry #dataengineer #analysis #career #code #pythoncode #datadriven #financialanalyst #developer #datacenter #businessanalysis #java #training #artificialintelligenceai #datasciences

Document Coordinator #datasciencetraining #dataviz #tableau #excel #programmer #coder #datascientists #analyst #machinelearningalgorithms #powerbi #digitalmarketing #datascienceeducation #datastructure #ml #dataentry #dataengineer #analysis #career #code #pythoncode #datadriven #financialanalyst #developer #datacenter #businessanalysis #java #training #artificialintelligenceai #datasciences #so

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