Project Engineer (0-1 Yrs) | Jaipur
Veeda Clinical ResearchJob Highlights
Required Skills
Job Description
Role Summary:
We are seeking a highly motivated and detail-oriented Project Engineer with a Doctorate/PhD to join our dynamic team in Jaipur. This entry-level position is ideal for a recent graduate looking to gain hands-on experience in managing and executing clinical research projects. The Project Engineer will work closely with senior project managers and cross-functional teams to ensure the successful planning, implementation, and completion of clinical trials, adhering to strict regulatory guidelines and timelines.
Key Responsibilities:
* Assist in the planning and execution of clinical research projects, from initiation to closure.
* Coordinate with internal teams (e.g., clinical operations, data management, regulatory affairs) and external stakeholders (e.g., investigators, vendors).
* Monitor project progress, identify potential risks and issues, and contribute to the development of mitigation strategies.
* Ensure adherence to Good Clinical Practice (GCP), applicable regulatory requirements, and company SOPs.
* Support in the preparation of project documentation, including study protocols, case report forms (CRFs), and progress reports.
* Assist in budget tracking and resource allocation for assigned projects.
* Participate in team meetings and provide updates on project status.
* Contribute to process improvement initiatives within the project management department.
* Conduct literature reviews and data analysis to support project objectives.
* Maintain accurate and organized project records.
About Veeda Clinical Research
Veeda Clinical Research is a leading Contract Research Organization (CRO) based in India, dedicated to providing comprehensive clinical research services to pharmaceutical and biotechnology companies worldwide. Established with a vision to bridge the gap between drug discovery and patient access, Veeda offers end-to-end solutions across various therapeutic areas. Our expertise spans early-phase clinical trials, late-phase clinical development, regulatory affairs, and data management. We are committed to upholding the highest standards of quality, integrity, and ethical conduct in all our operations, ensuring the safety and well-being of trial participants while delivering reliable and timely results to our clients.
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