Jobs at IQVIA

The role involves monitoring clinical sites, ensuring compliance with protocols, managing studies, and communicating with study teams and sites to improve recruitment and data integrity.

The role involves monitoring clinical trials, conducting site management, supporting recruitment initiatives, and ensuring compliance with regulations and guidelines.

Assist with administrative activities related to clinical trials, including maintaining documents, communication, and providing support for Clinical Research Associates and Regulatory teams.

Manage complex investigator grant estimates, contracting strategies, and compliance for clinical trials. Collaborate with stakeholders and develop training materials.

Manage the Order to Cash activities for projects, lead a small team, perform financial reporting, and ensure compliance with accounting standards.

Responsible for developing complex investigator grant estimates, contracting strategies, and coordination of investigator grants for clinical studies while ensuring compliance with regulatory requirements.

Seeking experienced Python Programmer with proficiency in PySpark and Pandas, strong SQL knowledge, and data visualization skills, preferably with Spotfire.

Assist Clinical Research Associates and Regulatory teams with maintaining clinical documents, coordinating data flow, and managing project communications. Mentor junior staff and may participate in recruitment.

Seeking experienced Statistical Programmers with expertise in ADaM and TFL programming. Experience in Oncology/Immunology and leadership in clinical studies required.

Provide advanced technical expertise in statistical programming, develop integrated programming solutions, and lead projects while mentoring team members.

The role requires developing and validating SDTM domains, CRF annotation, and knowledge of CDISC standards and regulatory delivery requirements.

The role involves managing O2C activities for projects, supporting stakeholders, analyzing financial metrics, and training a small team.

The role involves site monitoring, managing study data, ensuring compliance with regulations, and facilitating communication and training at research sites.

The role involves entering clinical data into management systems, processing clinical study documents, and ensuring compliance with guidelines while maintaining effective communication within the data management team.

Manage planning services for clinical research, develop enrollment strategies, lead meetings, mentor staff, and ensure compliance with clinical research regulations.

The role includes supporting project teams, maintaining documents, ensuring compliance with regulations, and mentoring new team members. It requires strong communication and planning skills.

The Clinical Research Associate performs monitoring and site management to ensure regulatory compliance and data integrity in clinical studies.

The Analyst will contribute to client projects and internal initiatives by conducting research, performing analyses, and preparing presentations. Responsibilities include developing recommendations, facilitating client workshops, and building relationships within the healthcare industry.

As a Scientist I, you will conduct antibody selections, validate libraries, execute molecular biology techniques, design genes, and collaborate with teams to improve processes.

The role involves data entry for clinical studies, reviewing records for accuracy, and coordinating monitoring visits while ensuring compliance with regulations.