Job Description
Seeking a Senior Process Executive with 1-2 years of experience in Clinical Data Management, Pharmacovigilance, and strong MS Excel skills.
Responsibilities:
Ensure data accuracy and compliance with regulatory standards in clinical data management.
Supervise data entry and validation tasks to maintain high-quality data standards.
Assist in preparing data reports and summaries for clinical trials.
Collaborate with cross-functional teams for seamless data integration.
Use MS Excel for analyzing, reporting, and visualizing data.
Ensure timely and accurate submission of data to regulatory authorities.
Help develop and maintain data management plans.
Monitor data quality and initiate corrective actions when needed.
Contribute to implementing best practices in data management.
Participate in process improvement initiatives to enhance efficiency in data handling.
Engage in training to stay updated with industry standards and best practices.
Maintain clear communication with team members and stakeholders for project alignment.
Provide technical support and troubleshoot issues related to data management systems.
Qualifications:
Strong technical proficiency in MS Excel for data analysis and reporting.
Domain expertise in Clinical Data Management and Clinical BPO.
Exceptional attention to detail and accuracy in handling data.
Expertise in data validation and maintaining quality control.
Excellent organizational and time management skills.
Effective communication and collaboration capabilities.
Proactive in problem-solving and process improvement initiatives.
Knowledge of regulatory requirements and industry standards.
Commitment to continuous professional learning and development.
Ability to work independently and as part of a team.
A bachelor’s degree in a relevant field or equivalent experience.
Experience with data management systems and related software.
Solid understanding of clinical trial processes and documentation.