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Company Description TCS Academy is a free program preparing artists for their journey through the world' s top visual effects studios through intensive training. Technicolor' s diversified reach in visual effects enables us to guide, mentor, and train these artists to meet the highest industry standards. Our courses prepare you for a career in visual effects by working with industry experts on your
Company Description TCS Academy is a virtual program preparing artists for their journey through the world' s top visual effects studios through intensive training. Technicolor' s diversified reach in visual effects enables us to guide, mentor, and train these artists to meet the highest industry standards. Our virtual courses prepare you for a career in visual effects by working with industry expe
Full Job DescriptionBe responsible for performing range of functions in the areas of technical design/review, development, deployment and integration of Business Intelligence amp; reporting solutions Be responsible for supporting the client's ability to collect, manage, and visualize vast amounts of data to influence decision-making at all levels Be responsible for designing reporting solutions cus
Novo Nordisk is looking for an experienced and motivated QA Lead to join our technology team. Novo Nordisk is a next-generation Platform-as-a-Service PaaS solution used by the top global pharmaceutical and healthtech companies for creating healthcare applications. As Lead - Quality Assurance, you will be responsible for leading and defining our QA processes and ensuring the quality of our products
Company Description TCS Academy is a free virtual program preparing artists for their journey through the world' s top visual effects studios through intensive training. Technicolor' s diversified reach in visual effects enables us to guide, mentor, and train these artists to meet the highest industry standards. Our virtual courses prepare you for a career in visual effects by working with industry
Company Description TCS Talent comprises a team of experts in recruitment, marketing and Lamp;D who work to meet the demands of the Technicolor' s brand across visual effects, advertising, creative experience and animation. We provide a central hub and the latest in job matching, job alerts, career guidance and development, thought leadership, learning opportunities and industry insights. By recogn
Prepare, compile amp; review Regulatory/Quality documents to support submissions to various markets Prepare deficiency responses, review labeling information, product monographs and marketing materials under supervision Prepare post approval supplements / annual reports to support changes and/or manage the regulatory product life cycle as applicable Seek guidance from other team members and manager
Full Job DescriptionJob Overview Will be responsible for the successful delivery of SFDC/OCE projects.Collaborating with Project Stakeholders for requirement understanding.Designing Technical solutions and workarounds for business requirements.Should mentor Juniors and handle training of new joiners. Essential Functions For assigned tasks, should formulate a proposed approach, plan - schedule and e
Full Job DescriptionJob Overview: Professional experience and strong knowledge with real time experience in Drug Safety Products from Oracle/Aris Global – Argus/ArisG Implementation/Upgrade/Maintenance of Drug Safety Application Working knowledge of writing SQL queries and/or PL/SQL code Excellent communication and inter-personal skills Commitment to excellence and high-quality standards Versatilit
Full Job DescriptionJob Overview Under general supervision, implement and maintain complex databases to meet customer requirements. Essential Functions Install and configure moderately complex databases in a server based environment.Facilitate database backup and recovery as well as documenting and testing all backup and recovery procedures.Manage all levels of database security and integrity, tra
Full Job DescriptionJob Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet contractual requirements in accordance with SOPs, policies and practices. Cli
PPD's Regulatory Medical Writing Services works closely with our clients around the world to develop and launch new medicines and treatments that improve healthcare for millions of patients. We' re one of the largest providers of medical writing services worldwide, and have managed thousands of writing projects in more than 29 countries across North and South America, Europe, Asia, and Africa. As a
PPD is a leading global contract research organization providing comprehensive, integrated drug development, laboratory and lifecycle management services. At PPD, we are passionate, deliberate, and driven by our purpose- to improve health Our colleagues in corporate strive for excellence in every task, at every moment. We are game changers seeking improvements to processes and more efficient ways
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),
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
Full Job DescriptionJob Overview Provides high quality, on-time input to client projects in the life sciences field. Assignments range in complexity from basic analysis and problem solving to assisting in the development of more complex solutions. May serve as project leader for small teams or work streams. Essential Functions Assists with the review and analysis of client requirements or problems
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
Full Job DescriptionPreparation of study trackers and updates to the sponsors Assist with preparation of study documentation under the guidance of the Project Manager.Liaise with external vendor to obtain translation of site/ patient documents, including initial quotesAssist with managing access requests to Connected Devices applications and databases Conduct biannual access review for Connected De
Follow applicable departmental Standard Operating Procedures, Work Instructions and departmental guidelines. Complete required trainings according to required timelines. Manage day-to-day tasks ensuring quality and productivity. Create and modify clinical investigator manuals, requisitions and other relevant materials according to SOW requirements to provide on-time, quality project related documen
The Associate Management Service Delivery is responsible for the day-to-day management and supervision of a Clinical Data Management team to ensure the successful implementation of the global data transmission strategy, structures, processes, and metrics in order to deliver outstanding customer satisfaction People Responsibilities: Supervise the day-to-day operations of the team members including
Collaborate and functionally report to Lead DM (LDM) for studies which include but not limited to - combination of healthy and patient populations, multi-site, medium complexity in protocol design or client management requirements. As a lead data reviewer and support to the lead Data Manager, you will perform all data operational tasks as appropriate to include, but not to be limited to data revie
Full Job Descriptionegulatory activities for selected studies or multi-protocol programs, including pre-award activities, oversight of the scope of work, budget and resources. Essential Functions Oversee the execution of Site Activation (including pre-award/bid defense activities) and/or Maintenance for assigned projects in accordance with the agreed RSU site activation strategy, adhering to proje
PPD's mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it's you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. We are passionate about being data and technically agile
Full Job DescriptionJob Overview Serve as the liaison between Records Management and user departments regarding Trial Master Files. Apply Records Management expertise to provide project related assistance across multiple project(s), sites, and project teams. May be required to ensure that project timelines are met and facilitate the orderly scanning, transfer, retention, and disposition of various
JOB DESCRIPTION PPD is now part of Thermo Fisher Scientific. 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. At PPD we develop ourselves and each other and recognize the power of being one team. We offer continued career a
Full Job DescriptionJob Overview Support the data processing function for the maintenance of the QA database(s) supporting the auditing system lifecycle programs and processes across all Global QA business units. Essential Functions Maintain the QA database(s) ensuring Audits when identified are entered onto the system from audit plans/notification documentation and The system is updated as requir
Serves as a member of the project team with primary responsibilities for all testing and documentation, requirements to support global EDC solutions tasks. Create and Execute validation test scripts as requested and document the test results. Supports validation activities as assigned and serves as a validation team member. Review to make oneself familiar with the Validation specifications. Wri
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
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 DescriptionJob Overview Conduct and/or support audits and report preparation/distribution, Support quality issues management, Customer Audit/ Regulatory Inspections hosting, Corrective and Preventative Action (CAPA) and Effectiveness Check (EC) plan review, approval and closure and Audit plan development. Provide consultation in interpretation of regulations, guidelines, policies, and proc
JOB DESCRIPTION PPD's mission is to improve health. It starts as an idea to find a cure. It becomes a life saved. All in-between, it's you! We know that meaningful results not only require the right approach, but also the right people. We invite you to re-imagine health promoting protocols with us, working alongside our talented, bright and energetic teams. We are passionate about being data and
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