4 Gcp Knowledge Jobs

Imaging Endpoints (IE) is an Imaging Technology and Imaging Clinical Research Organization (iCRO) with a passionate focus on connecting imaging to the cure. Our daily work is dedicated to advancing imaging science, technology, and services to bring curative technologies to humankind. We have played a crucial role in supporting new drug approvals in oncology and are continuously seeking talented individuals globally who share our passion for customizing each clinical trial's imaging to optimize efficacy. Based in various locations including Scottsdale, Arizona; Cambridge, Massachusetts; London, UK; Leiden, Netherlands; Basel, Switzerland; Hyderabad, India; and Shanghai, China, Imaging Endpoints is affiliated with HonorHealth and Scottsdale Medical Imaging Limited (SMIURadPartners). We are recognized as the world's largest and most preeminent iCRO in oncology. As a Clinical Trial Imaging Specialist, you will work under the direction of Imaging Operations Management to conduct quality control/analysis procedures and read assignments according to study-specific protocols. Your responsibilities will include reviewing imaging data from clinical trial sites to ensure protocol requirements are met, technical adequacy is maintained, and data integrity is preserved. Additionally, you will support project management tasks within the operations department and provide technical imaging support to both internal and external staff. **Responsibilities:** - Perform technical quality review and quantitative image analysis as per trial specifications - Reconcile imaging data according to trial specifications - Manage research projects and early phase clinical trials on a day-to-day basis - Complete quality control documentation in adherence to standard operating procedures - Develop quality control documentation in collaboration with the Project Manager - Generate, track, and resolve image queries promptly to address technical issues - Identify and assign cases for read assignment based on SOP and SSP - Prepare study dossiers associated with read assignment per SOP/SSP - Track read assignment status and additional information in Clinical Trial Management Systems (CTMS) - Provide support to clinical sites and imaging centers - Develop training materials and conduct technical training for imaging site personnel - Assist in writing site imaging manuals and maintain Trial Master File (TMF) for audit readiness - Assist in training internal staff and perform any other duties assigned by the manager **Education and Experience:** - Bachelor's degree in a science or health-related field or Registered Technologist (R.T.) with advanced modality experience in CT, MRI, or Nuclear Medicine preferred - Proficiency in MS Office and internet applications required - Minimum of 2 years of experience in medical imaging, with at least 1 year in the clinical trials industry preferred - Knowledge of Good Clinical Practice (GCP) and Quality Assurance/Compliance in a clinical trials setting preferred - Familiarity with image trial documents such as Image Review Charter, Imaging Manual, Data Transmittal Forms, etc., strongly preferred As a Clinical Trial Imaging Specialist II, your responsibilities will include conducting technical quality reviews, quantitative image analysis, resolving image queries, preparing study dossiers, tracking read assignment status, and communicating with readers and the study team as needed. You will also be involved in operational process improvements, client meetings, and other duties assigned by the manager. **Education and Experience:** - Bachelor's degree in a science or health-related field or Registered Technologist (R.T.) with advanced modality experience in CT, MRI, or Nuclear Medicine preferred - Proficiency in MS Office and internet applications required - Minimum of 3 years of experience in medical imaging, with at least 2 years in the clinical trials industry preferred - Knowledge of GCP, Quality Assurance/Compliance, and the drug development process in a clinical trials setting preferred - Familiarity with image trial documents strongly preferred **Skills:** - Proficiency in MS Office and internet applications - Service-oriented approach, flexibility, and proactive attitude towards client needs - Ability to manage project activities with little supervision - Superior attention to detail with excellent oral and written communication skills - Independent work ability, multitasking skills, and meeting critical deadlines under pressure - Strong time management, organization, and self-motivation - Team player mindset with strict compliance to procedures and regulations - Ability to maintain confidentiality and grasp new concepts quickly - Prioritization skills for changing business needs - Understanding of technical research protocols and leadership within the research environment **Imaging Endpoints" Team Characteristics:** - Passionate about connecting imaging to the cure and improving cancer patients" lives - Desire to be part of a dynamic, global team dedicated to helping humanity through imaging - Commitment to caring for team members, families, and communities IE serves - Upholding integrity, high ethical standards, and a focus on excellence - Structured, organized, detail-oriented, and self-motivated approach - Accountability, effective communication, and a high standard for quality **Physical Requirements:** While performing job duties, you will be required to use hands, sit, and have specific vision abilities. Travel may be required up to 5-10% domestically or internationally. If you are seeking a rewarding career in a fast-paced environment where your contributions can make a real impact, consider joining our team at Imaging Endpoints.,

About the client: Our client is a global IT services company headquartered in Southborough, Massachusetts, USA. Founded in 1996, with a revenue of $1.8B, and 35,000+ associates worldwide, the company specializes in digital engineering and IT services, helping clients modernize their technology infrastructure, adopt cloud and AI solutions, and accelerate innovation. Our client partners with major firms in banking, healthcare, telecom, and media. Known for combining deep industry expertise with agile development practices, the company enables scalable and cost-effective digital transformation. With operations in over 50 locations across more than 25 countries, delivery centers in Asia, Europe, and North America, and backing from Baring Private Equity Asia. Job Title: ETL Developer With DBA Key Skills: ETL development, data modeling, DataStage (ETL), R language (Must have), Linux scripting, SQL, Control-M Job Location: Hyderabad Experience: 4-6 years Education Qualification: Any Graduation Work Mode: Hybrid Employment Type: Contract Notice Period: Immediate Job Responsibilities: The candidate should have 8 years and above experience in ETL development. Understanding of data modeling concepts. Passionate about sophisticated data structures and problem solutions. Quickly learn new data tools and ideas. Proficient in skills - DataStage (ETL), R language (Must have), Linux scripting, SQL, Control-M. GCP knowledge would be an added advantage. The candidate should be well aware of Agile ways of working. Knowledge of different SQL/NoSQL data storage techniques and Big Data technologies.,

The Manager of Clinical Research will lead and manage clinical trials and research studies to ensure timely completion within budget and compliance with regulatory standards. Supervising research teams, collaborating with cross-functional departments, and providing strategic direction for clinical research activities are key responsibilities. You will be responsible for planning, initiating, and managing clinical research projects from start to finish. Coordinating and overseeing the execution of clinical trials, ensuring adherence to protocols, timelines, and budgets is essential. Compliance with Good Clinical Practice (GCP), regulatory requirements, and ethical standards must be ensured. Oversight on recruitment, enrollment, and monitoring of clinical trial subjects is part of the role. Managing relationships with clinical research organizations (CROs), investigators, and external vendors is key. Leading and mentoring clinical research staff, ensuring effective performance, assigning tasks based on project needs, and providing ongoing professional development are critical leadership responsibilities. Additionally, overseeing regulatory documentation, monitoring compliance with regulations and company policies, and ensuring timely reporting of adverse events are important aspects of the role. Collaboration with scientific and medical teams to develop clinical trial protocols, ensuring adherence to study objectives, regulatory standards, and ethical guidelines, and evaluating feasibility and risk of proposed studies are part of the responsibilities. Data management, reporting, preparing progress reports, budget management, resource allocation, fostering communication between teams, partners, and stakeholders, resolving issues related to study execution, identifying areas for process improvement, and implementing best practices are key components of this role. Qualifications for this position include a Bachelor's degree in Life Sciences, Clinical Research, or related field (Master's or higher preferred), 2-3 years of experience in clinical research, in-depth knowledge of clinical trial management, regulatory requirements, and GCP. Skills required include project management, leadership, organizational skills, communication, interpersonal skills, proficiency in clinical research software, problem-solving, and decision-making abilities. Clinical Research Coordinator (CRC) or Clinical Research Associate (CRA) certification preferred. This full-time position may be in-office or remote, with occasional travel required to clinical trial sites and partner organizations.,

About VOIS: VO IS (Vodafone Intelligent Solutions) is a strategic arm of Vodafone Group Plc, creating value and enhancing quality and efficiency across 28 countries, and operating from 7 locations: Albania, Egypt, Hungary, India, Romania, Spain and the UK. Over 29,000 highly skilled individuals are dedicated to being Vodafone Group's partner of choice for talent, technology, and transformation. We deliver the best services across IT, Business Intelligence Services, Customer Operations, Business Operations, HR, Finance, Supply Chain, HR Operations, and many more. Established in 2006, VO IS has evolved into a global, multi-functional organisation, a Centre of Excellence for Intelligent Solutions focused on adding value and delivering business outcomes for Vodafone. About VOIS India: In 2009, VO IS started operating in India and now has established global delivery centres in Pune, Bangalore and Ahmedabad. With more than 14,500 employees, VO IS India supports global markets and group functions of Vodafone, and delivers best-in-class customer experience through multi-functional services in the areas of Information Technology, Networks, Business Intelligence and Analytics, Digital Business Solutions (Robotics & AI), Commercial Operations (Consumer & Business), Intelligent Operations, Finance Operations, Supply Chain Operations and HR Operations and more. Job Description Role purpose: Creating detailed data architecture documentation, including data models, data flow diagrams, and technical specifications Creating and maintaining data models for databases, data warehouses, and data lakes, defining relationships between data entities to optimize data retrieval and analysis. Designing and implementing data pipelines to integrate data from multiple sources, ensuring data consistency and quality across systems. Collaborating with business stakeholders to define the overall data strategy, aligning data needs with business requirements. Support migration of new & changed software, elaborate and perform production checks Need to effectively communicate complex data concepts to both technical and non-technical stakeholders. GCP Knowledge/exp with Cloud Composer, BigQuery, Pub/Sub, Cloud Functions. -- Strong communicator, experienced in leading & negotiating decision and effective outcomes. -- Strong overarching Data Architecture knowledge and experience with ability to govern application of architecture principles within projects VOIS Equal Opportunity Employer Commitment India: VO IS is proud to be an Equal Employment Opportunity Employer. We celebrate differences and we welcome and value diverse people and insights. We believe that being authentically human and inclusive powers our employees growth and enables them to create a positive impact on themselves and society. We do not discriminate based on age, colour, gender (including pregnancy, childbirth, or related medical conditions), gender identity, gender expression, national origin, race, religion, sexual orientation, status as an individual with a disability, or other applicable legally protected characteristics. As a result of living and breathing our commitment, our employees have helped us get certified as a Great Place to Work in India for four years running. We have been also highlighted among the Top 10 Best Workplaces for Millennials, Equity, and Inclusion , Top 50 Best Workplaces for Women , Top 25 Best Workplaces in IT & IT-BPM and 10th Overall Best Workplaces in India by the Great Place to Work Institute in 2024. These achievements position us among a select group of trustworthy and high-performing companies which put their employees at the heart of everything they do. By joining us, you are part of our commitment. We look forward to welcoming you into our family which represents a variety of cultures, backgrounds, perspectives, and skills! Apply now, and we'll be in touch!