Clinical Data Management Team Lead

4 weeks ago


Bengaluru, Karnataka, India IQVIA Full time

Job Overview
At IQVIA, we are seeking a highly skilled Clinical Data Management Team Lead to manage and support a team of Data Management professionals. The successful candidate will be responsible for efficiently producing databases that meet customer requirements.

Key Responsibilities
• Manage a team of professional Data Management staff, defining and prioritizing resource requirements and managing resource assignments across projects.
• Directly responsible for utilization of staff, assessing and documenting competency to satisfy position responsibilities, and regularly setting goals and evaluating performance.
• Propose salaries, promotion, and termination actions, and actively contribute to recruitment of new staff.
• Provide expert review and guidance for production of Data Management deliverables, including CRF/e-CRF, database design and set-up, validation definition and programming, Data Management Plan, and database deliverables to internal and external customers.
• Participate in the development and implementation of new processes and technology, ensuring staff is trained and compliant with current operating procedures and work instructions and project scope of work.

Requirements
• Bachelor's Degree in Clinical, biological, or mathematical sciences or related field, or nursing qualification.
• 7 years of relevant work experience, including people management, with advanced knowledge of Data Management processes and systems, and solid understanding of clinical drug development process.



  • Bengaluru, Karnataka, India IQVIA Full time

    **Job Overview**As a Clinical Data Management Team Lead at IQVIA, you will be responsible for managing and supporting a team of Data Management professionals to efficiently produce databases that meet customer requirements.**Key Responsibilities**Manage a team of professional Data Management staff, defining and prioritizing resource requirements and managing...


  • Bengaluru, Karnataka, India IQVIA Full time

    Job OverviewAt IQVIA, we are seeking a highly skilled Clinical Data Management Team Lead to manage and support a team of Data Management professionals. The ideal candidate will have a proven track record of efficiently producing databases that meet customer requirements.Key Responsibilities:• Manage a team of professional Data Management staff, defining...


  • Bengaluru, Karnataka, India MUM Fortrea Development India Pvt Ltd Full time

    About the Role:Fortrea is seeking a Clinical Data Management Lead to join our team in India. As a Clinical Data Management Lead, you will be responsible for leading clinical data management activities for multiple projects, including the development of data management plans, data cleaning and validation, and data reporting.Key Responsibilities:Lead clinical...


  • Bengaluru, Karnataka, India George Clinical Full time

    We are a leading global clinical research organization seeking a highly skilled Clinical Research Professional to join our team. The successful candidate will be responsible for providing medical and academic input to various aspects of our studies, ensuring project delivery is of high quality, operationally aligned, cost-effective, and competitive.Key...


  • Bengaluru, Karnataka, India Quanticate Full time

    Job Title: Lead CDM ProgrammerQuanticate is a leading data-focused Clinical Research Organization (CRO) that works with pharmaceutical, biotechnology, and medical device companies to provide expert data management, statistical programming, and clinical trial reporting services.We are seeking a highly skilled and experienced Lead CDM Programmer to join our...


  • Bengaluru, Karnataka, India Precision Medicine Group Full time

    At Precision Medicine Group, we are driven by a shared passion to revolutionize the way clinical trials are conducted.The field of precision medicine is rapidly evolving, and we need talented professionals like you to help us stay ahead of the curve.This role is an excellent opportunity for a seasoned SAS programmer to take on new challenges and lead...


  • Bengaluru, Karnataka, India George Clinical Full time

    Role Summary:George Clinical is seeking a highly skilled Clinical Research Specialist to join our team. As a Clinical Research Specialist, you will provide medical and academic input to various aspects of George Clinical studies.Key Responsibilities:Provide medical and academic expertise for new and existing George Clinical studies.Support Endpoint...


  • Bengaluru, Karnataka, India Kenvue Full time

    About the RoleWe are seeking a highly skilled Manager, Clinical Pharmacology to join our team at Kenvue. As a key member of our Clinical Pharmacology team, you will be responsible for providing clinical pharmacology support for innovation projects, developing and delivering clinical pharmacology strategies for assigned Clinical Research projects, and serving...

  • Global Legal Expert

    4 days ago


    Bengaluru, Karnataka, India George Clinical Full time

    George Clinical is a leading global clinical research organization driven by scientific expertise and operational excellence. With over 20 years of experience, our team manages 39+ geographical locations throughout the Asia-Pacific region, USA, and Europe, offering full-range clinical trial services to biopharmaceutical, medical device, and diagnostic...


  • Bengaluru, Karnataka, India Allucent Full time

    Company OverviewAllucent is a leading company in the biopharmaceutical industry, dedicated to helping small-medium companies navigate the complex world of clinical trials. With a focus on quality and customer satisfaction, Allucent aims to bring life-changing therapies to patients worldwide.About the RoleWe are seeking an experienced Clinical Data Management...


  • Bengaluru, Karnataka, India George Clinical Full time

    We are expanding our global clinical research capabilities and are seeking a highly skilled medical professional to join our team as a Medical Monitor. As a Medical Monitor, you will be responsible for providing medical and academic input to various aspects of our clinical studies, ensuring project delivery is of high quality, operationally aligned,...


  • Bengaluru, Karnataka, India Parexel Full time

    About the RoleThe Senior Clinical Data Analyst will lead and coordinate all clinical data validation activities on assigned projects, with a high degree of proficiency and autonomy.Key Responsibilities include:Performing data validation (cleaning/review/reconciliation) activities during conduct and database lockHighlighting issues/risks to delivery by...


  • Bengaluru, Karnataka, India MUM Fortrea Development India Pvt Ltd Full time

    Job SummaryFortrea Development India Pvt Ltd is seeking a highly skilled Clinical Data Specialist to join our team. As a Clinical Data Specialist, you will be responsible for reviewing clinical trial data in accordance with global data management plans and applicable standardized data management processes. You will identify erroneous, missing, incomplete, or...


  • Bengaluru, Karnataka, India Excelya Full time

    Excelya, a leading Contract Research Organization (CRO) in Europe, is seeking a Clinical Data Manager to join our team.As a Clinical Data Manager, you will be responsible for performing Data Management tasks per client work orders to high regulatory standards and Client's SOPs.The role involves:Deeply acknowledging and strictly following applicable Excelya...

  • Clinical Data Manager

    3 weeks ago


    Bengaluru, Karnataka, India MUM Fortrea Development India Pvt Ltd Full time

    We are looking for a Clinical Data Manager to lead our team in the delivery of high-quality clinical data management services. The successful candidate will have a strong background in clinical data management, with experience in managing data-focused internal project teams and collaborating with peers to deliver complex projects.Key Responsibilities:Lead...


  • Bengaluru, Karnataka, India BAN Fortrea Clinical Development Pvt Ltd Full time

    Job SummaryWe are seeking a highly motivated and detail-oriented Clinical Trials Coordinator to join our team at BAN Fortrea Clinical Development Pvt Ltd. The successful candidate will be responsible for coordinating clinical trials activities, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams.Key...


  • Bengaluru, Karnataka, India MUM Fortrea Development India Pvt Ltd Full time

    Job DescriptionJob Title: Clinical Data SpecialistMUM Fortrea Development India Pvt Ltd is seeking a highly skilled Clinical Data Specialist to join our team.Responsibilities:Review clinical trial data in accordance with global data management plans and applicable standardized data management processes.Run ancillary programs to support data review...


  • Bengaluru, Karnataka, India MUM Fortrea Development India Pvt Ltd Full time

    Transform drug and device development for our global partners and patients. We are seeking a highly motivated Clinical Data Specialist to join our team.About FortreaAs a leading global contract research organization (CRO) with a passion for scientific rigor, we provide pharmaceutical, biotechnology, and medical device customers a wide range of clinical...


  • Bengaluru, Karnataka, India MUM Fortrea Development India Pvt Ltd Full time

    Company Overview">Fortrea, a leading global contract research organization (CRO), is dedicated to scientific rigor and decades of clinical development experience.We provide pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across over 20 therapeutic areas.With a...


  • Bengaluru, Karnataka, India MUM Fortrea Development India Pvt Ltd Full time

    Job SummaryWe are seeking a Clinical Data Specialist to join our team at MUM Fortrea Development India Pvt Ltd. As a Data Management Specialist, you will be responsible for ensuring the quality and integrity of clinical trial data.Main ResponsibilitiesEnsure all allocated projects are carried out in accordance with relevant protocols, SOPs, and GCP...