Veeva Developer - Blue Bell

+We are looking for a skilled Veeva Developer to join our team on a long-term contract basis.+ · +Develop and maintain Veeva-focused applications tailored to client requirements. · Manage a queue of development tasks, ensuring timely and accurate completion. · Participate in week ...

We are looking for a skilled Veeva Developer to join our team on a long-term contract basis. · Develop and maintain Veeva-focused applications tailored to client requirements. · Manage a queue of development tasks, ensuring timely and accurate completion. · ...

+Veeva Integration Developer with hand on experience in Informatica power centre. Should be well versed in migration activities. · +Maintaining daily connect with the business analyst and Offshore team. · Building & Delivering high quality code meeting the industry best practices ...

Veeva Integration Developer with hand on experience in Informatica power centre. Should be well versed in migration activities. · Close cooperation with business representative/business analyst on understanding of user's standalone or project-related needs. · Maintaining daily co ...

This is a technical role requiring experience in Veeva Vault development with system integrations using middleware design patterns with Vault eTMF. · ...

Establish and ensure strategic alignment with stakeholders for Veeva CRM platform and long-term scalability for clients in the pharmaceutical industry. Author user acceptance test scripts and summaries. · ...

Veeva Business Analyst - SS103: Establish strategic alignment with stakeholders for Veeva CRM platform. · Author user acceptance test scripts and summaries. · Facilitate UAT, perform quality assurance, prepare validation documents to manage daily project activities. · ...

The Senior Clinical Trial Associate will support all phases of clinical trial activities under the direction and supervision of Clinical Operations Lead(s). Plans, supports, and communicates clinical trial timelines. Ensures consistency of processes across clinical trials. · Bach ...

We're proud to foster an inclusive environment driving innovation and excellence. · 4+ years in the pharmaceutical or clinical research industry. · Bachelor's Degree or international equivalent required; Life Sciences preferred. · ...

The Senior Clinical Trial Associate will support all phases of clinical trial activities under the direction and supervision of Clinical Operations Lead(s). Plans, supports and communicates clinical trial timelines. Ensures consistency of processes across clinical trials. · Condu ...

+ 5-10% travel, including overnight and international travel to client sites.Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family. · Provide subject matter expertise in ICF develo ...

+Clinical Study Associate at ICON plc. · +Provide support for critical day to day clinical study activities. · Collaborate with CSA colleagues and study teams. · +QualificationsBachelor's degree in Life Sciences or a related field. · ...

The Study Start Up Associate II conducts clinical trial site start-up activities related to the preparation and approval of regulatory documents, ensuring they are conducted consistent with service level agreements, legal and regulatory standards, and applicable company policies ...

We are seeking a Senior Software Engineer with strong full-stack development skills to design, implement, and lead end-to-end integrations across R&D domains and the Veeva RIM platform. · Design integration of cloud AI capabilities (model deployment, feature stores, inference pip ...

+We are seeking a Senior Software Engineer with strong full-stack development skills to design, implement, and lead end-to-end integrations across R&D domains and the Veeva RIM platform. · Design integration of cloud AI capabilities (model deployment, feature stores, inference pi ...

This position is for a Sr Release Management Engineer to lead execution and coordination of release activities related to projects or services. The job involves coordinating day-to-day operations, maintenance of source code repositories and enforcement of release standards. · Lea ...

Implement CRM business requirements into Veeva System. · Administration, customization, configuration and data migration on Veeva · Generate various reports on Veeva · ...

A Business Analyst with strong Veeva and Medcomm experience required. · Work closely with Business Partners to help them in business processes Liaise with Business teams to understand Client's processes and document precisely for NewCo Review SIT scenarios to ensure the proposed ...

The Medical Writer Contractor is responsible for creating external tools and resources for scientific exchange and in response to medical information inquiries. · ...

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