1036 Edc Jobs - Page 42

Role: We are hiring energetic and self-driven individuals for Sales Officer role in the Merchant Acquisition Business. Contact Person - Harish (8089302900) Responsibilities : Identify and onboard merchants from the open market Promote and sell POS machines (Point of Sale) Achieve daily/monthly sales targets Ensure timely documentation and activation Maintain strong merchant relationships Who can apply : Any open market experience would be preferred Two-Wheeler is mandatory Must be graduated Regards, Team HR

Data governance/Data OPS Informatica Admin, AXON & EDC Exposure in architecting a data governance solution at the enterprise level using Informatica tool AXON. Must be able to integrate with other tools and Informatica tools like EDC, IDQ etc. Required Candidate profile Should be able to understand the business context and translate this into AXON templates and facet

Major Accountabilities Provides DM support across multiple (4 or more) assigned trial(s). Acts as the Trial Data Manager for 1 trial in sequence where needed Provides feedback to assure well-developed databases and data validation setup and execution while making the best use of standards and best practices Supports the team through database build requirements and complete startup activities for study including: building the eCRF, completion guidelines, standard and simple rules, data validation plan and user acceptance testing (UAT); can lead a study in sequence under PCDM supervision. Set up and manages external data in accordance with protocol requirements, process and validation requirem...

ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS Develop eCRF (database setup) for late phase projects Create CDM documents (like DMP, DVP, eCCG, etc.) Program edit checks as per data validation requirements Perform medical coding and Query Management activities Sharing of CDM updates ...

ORGANISATIONAL OVERVIEW Lambda Therapeutic Research is a Global full-service Clinical Research Organization (CRO) with its headquarters in Ahmedabad, India. With facilities and operations strategically located in Mehsana (India), Las Vegas (USA), Toronto (Canada), Barcelona (Spain), London (UK) and Warsaw (Poland), we offer comprehensive end-to-end clinical research services to the global innovator, biotech, and generic pharmaceutical industries. JOB DETAILS Develop eCRF (database setup) for late phase projects Create CDM documents (like DMP, DVP, eCCG, etc.) Program edit checks as per data validation requirements Perform medical coding and Query Management activities Sharing of CDM updates ...

Monitor and document all adverse events (AEs) and serious adverse events (SAEs) in accordance with study protocol, sponsor requirements, and applicable regulations. Ensure timely and accurate reporting of SAEs to the Ethics Committee, Sponsor, and Regulatory Authorities as required. Assist clinical staff in the identification, documentation, and classification of safety events. Maintain up-to-date safety tracking logs and ensure proper storage of safety documentation. Participate in safety review meetings and contribute to the preparation of safety summaries and reports. Liaise with investigators, data managers, and monitors to reconcile discrepancies related to safety data. Assist with trai...

We are seeking a qualified and experienced Paediatrician to support clinical activities in a paediatric-focused clinical trial and community-based health study. The Paediatrician will play a central role in participant assessment, monitoring safety, managing clinical care, and contributing to data quality and protocol adherence. Key Responsibilities: Conduct clinical evaluations and physical examinations of paediatric participants. Assess eligibility and screen potential participants according to protocol criteria. Monitor participant health throughout the study and manage adverse events as per Good Clinical Practice (GCP). Prescribe treatments and interventions per protocol and standard ped...

Overview Job Summary: This position is responsible for configuring, managing, and supporting clinical research teams in data entry and validation, and ensuring adherence to regulatory and sponsor requirements. The EDC Coordinator will work closely with the site staff to optimize electronic data workflows and maintain data integrity. Responsibilities Duties/Responsibilities: Support clinical research site staff with accurate data entry, query resolution, and validation checks to ensure data quality. Ensure data management processes adhere to Good Clinical Practice (GCP), FDA, and sponsor-specific regulations. Monitor data discrepancies, perform data cleaning activities Work closely with clini...

JOB DESCRIPTION Job Title: Clinical Data Management QA Auditor Job Location: Semicon Park About Syngene : Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and...

JOB DESCRIPTION Job Title: Clinical Trial Management - QA Job Location: Bangalore About Syngene : Syngene ( www.syngeneintl.com ) is an innovation-led contract research, development and manufacturing organization offering integrated scientific services from early discovery to commercial supply. Mandatory expectation for all roles as per Syngene safety guidelines Overall adherence to safe practices and procedures of oneself and the teams aligned Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company s integrity & quality standards Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operati...

This position is responsible for configuring, managing, and supporting clinical research teams in data entry and validation, and ensuring adherence to regulatory and sponsor requirements. The EDC Manager will work closely with the site staff to optimize electronic data workflows and maintain data integrity. Responsibilities Duties/Responsibilities: Support clinical research site staff with accurate data entry, query resolution, and validation checks to ensure data quality. Ensure data management processes adhere to Good Clinical Practice (GCP), FDA, and sponsor-specific regulations. Monitor data discrepancies, perform data cleaning activities Work closely with clinical research teams, sponso...