

I will be in that organization where they will value my skills and hard work. Logical Clinical Research Associate with background identifying, assessing and preventing adverse effects or medications, vaccines and related pharmaceutical items. Dedicated expert with focus on maintaining drug safety by preparing and reviewing data and reports. Meticulous when authoring professional documents and reviewing scientific literature. Organized and dependable candidate successful at managing multiple priorities with a positive attitude. Willingness to take on added responsibilities to meet team goals. To seek and maintain full-time position that offers professional challenges utilizing interpersonal skills, excellent time management and problem-solving skills.
Pharmacovigilance in Clinical Research
Jadavpur University
Data Science using Python and R
Nielit Jadavpur University
Medical terminology knowledge
Drug safety expertise
Continuous learning mindset
Pharmacovigilance Regulations
Case processing abilities
Quality Assurance Techniques
Clinical trial monitoring
Scientific literature review
Signal detection proficiency
Critical Thinking
Time management abilities
Self Motivation
Decision-Making
Multitasking Abilities
Excellent Communication
Multitasking
Data Entry
Problem-solving abilities
Test Results Interpretation