Job Description

https://jobs.iqvia.com/

Provide project related assistance to assigned project teams. Ensure all work is conducted in

accordance with standard operating procedures, policies, good clinical practices and applicable

regulatory requirements. Meeting quality and timeline metrics.

Essential Functions

• Complete appropriate role-specific training to perform job duties.
• Perform assigned tasks to support team members with project execution (examples of such
• tasks include but not limited to running system reports, preparing and distributing status reports,
• creating and maintaining study documents, etc.).
• Interact with sites/clinical research associate and follow-up of missing data, pending queries,
• source data verification backlog, visit schedule, protocol deviations, etc.
• Assist in preparation of i-site pack for respective sites and countries for assigned studies.
• Perform the activities as per the task list delegated by Centralized Monitoring
• Specialist/Centralized Monitoring Lead.
• Assist in updating and maintaining data in systems within project timelines and per project
• requirement.
• Establish and maintain effective project/site communication.
• Create and maintain relevant project documents.
• Ensure accurate completion and maintenance of internal systems, databases, tracking tools and project plans.
• Act as a backup for Central Monitors

Qualifications

• Other Graduate/Post Graduate in Life Sciences or related field.
• Requires minimum of 2 to 5 years of work experience with minimum of 1 year relevant
• Experience .equivalent combination of education, training and experience. Experience level may vary based on customer specific requirements.
• Good knowledge of applicable clinical research regulatory requirements.
• i.e., International Conference on Harmonisation - Good Clinical Practice and relevant local
• laws, regulations and guidelines.
• Proficient in Clinical Systems (good knowledge on electronic data capture (EDC), interactive X
• response system (IXRS), clinical trial management system (CTMS) or equivalent systems).
• Experience of managing global phase trials and clinical trial systems and/or reviewing clinical
• trial data.
• Strong written and verbal communication skills including good command of English language.
• Results and detail-oriented approach to work delivery and output.
• Good problem-solving skills.
• Good planning, time management and prioritization skills.
• Attention to detail and accuracy in work.
• Good software and computer skills, Microsoft Office applications including but not limited to Microsoft Word, Excel and PowerPoint.
• Ability to establish and maintain effective working relationships with coworkers, managers and clients.
• Strong telecommunication skills.
• Good data entry skills

Skills Required: Health Care,Clinical Research,Pharma,Biotech,Biotechnology,Life Sciences,Clinical Research Associate,Clinical Research Assistant