Gayathri
Hourly rate: members only
Availability: members only
Willingness to travel: Within the UK
Professional status: Freelancer
Last updated: 21 Apr 2025
Total work experience:
Language skills: English, Hindi,
Personal summary
I am a dedicated Safety Operations Specialist with over 3 years of hands-on experience in pharmacovigilance and clinical research. My expertise lies in ensuring regulatory compliance, managing adverse event data, and maintaining high standards of data integrity. I bring strong proficiency in tools like Argus, CDMS, Medidata Rave, and Veeva Vault, along with a solid background in MedDRA coding and ICSR processing. Throughout my career at organizations such as IQVIA and TCS, I have collaborated with cross-functional teams, streamlined reporting processes, and enhanced client communication. With a Master’s in Clinical Research and multiple certifications in pharmacovigilance and GMP, I am well-equipped to contribute to global safety operations. I am detail-oriented, proactive, and thrive in fast-paced environments where accuracy and compliance are critical.
Language skills
English
Fluent knowledge
Hindi
Fluent knowledge