We're Hiring: Global Project Manager in Clinical Research!
🌟 We're Hiring: Global Project Manager in Clinical Research! 🌟
Organization Overview:
Cliantha Research, a full-service Clinical Research Organization (CRO) in Ahmedabad, India, upholds the motto "Science with Integrity." With over 15 years of regulatory compliance, Cliantha collaborates with global agencies including the USFDA, WHO, MHRA, Health Canada, and NABL, offering comprehensive clinical research services.
Position: Global Project Manager
Company: Cliantha Research
Location: Ahmedabad, India
Experience: Freshers (0-1 Year of experience)
Salary: 2.5 - 4.5 LPA
Education: B.Pharm, M.Pharm, Pharm.D, M.Sc, B.Sc, Life Sciences
If you're a fresh graduate looking to kick-start your career in clinical research and project management, this is a fantastic opportunity for you! At Cliantha Research, we’re seeking motivated individuals with a passion for managing projects, ensuring compliance, and working closely with cross-functional teams. 🚀
Key Responsibilities 🎯
Project Planning & Monitoring 🗓️: You'll be responsible for planning, organizing, and tracking project activities using our Project Management (PM) database. This role includes coordinating across various teams to maintain high accuracy and ensuring that all activities are completed on time.
Managing Critical Path Activities ⏳: Identify and manage time-sensitive tasks crucial to project success. You'll be instrumental in aligning project activities with critical milestones set by the FDA, focusing on quality and compliance throughout the process.
Software & Database Support 💻: Provide initial support in PM software issues. This involves troubleshooting, documenting solutions, and facilitating smooth project operations through database management.
Training & Process Improvement 📈: Train new end-users on our processes and gather valuable feedback for process improvements. Your role will also include suggesting enhancements that can help streamline activities and improve project efficiency.
Data Management 📊: Keep records up-to-date for analytical methods and bioequivalence (BA/BE) studies, ensuring data accuracy and compliance with industry standards.
Who We're Looking For 🕵️♂️
Educational Background:
Fresh graduates are welcome! A strong foundation in BA/BE studies is an asset, and degrees in Pharmacy, Life Sciences, or related fields are highly preferred.
Skills:
We're looking for someone with strong organizational, communication, and project management skills. Familiarity with BA/BE regulatory guidelines and experience in using PM software are a plus.
Profile:
This role is ideal for freshers interested in a career in clinical research and project management, with a particular focus on compliance and quality.
👉 If you're ready to dive into an exciting career in clinical research project management and have a passion for ensuring quality and efficiency, we want to hear from you!
Send your resume to:
vdesai@cliantha.com | mjunnarkar@cliantha.com
Don’t miss this opportunity to build a strong foundation in clinical research with Cliantha Research. Apply now and embark on a rewarding journey! 🌟
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