Yogananth A S
Bangalore
Summary
As an experienced professional in clinical and scientific research, I am eager to join your esteemed organization to further develop my skills in a dynamic environment. With keen attention to detail, strategic thinking, and a focused demeanor, I am prepared to make meaningful contributions to your team and drive towards enhanced outcomes.
Overview
6
6
years of professional experience
1
1
Certification
Work History
Senior Research Associate
St.Johns National Academy Of Health Sciences
Bengaluru
01.2024 - Current
- Collaborate closely with study teams to review, revise, and compose protocols, Case Report Forms (CRF), and other essential documentation for clinical research studies.
- Engage with Clinical Research Organizations (CRO) and study teams to draft, assess, and amend Informed Consent Forms (ICF).
- Support the oversight of daily operations in clinical research studies to ensure prompt commencement, enrollment, upkeep, and closure of designated studies.
- Aid in the instruction and oversight of newly recruited Clinical Research Associates (CRAs).
- Scrutinize informed consent forms and other Trial Master File (TMF) documents to ensure compliance with regulatory standards.
- Conduct site visits as necessary to verify adherence to ICH/GCP guidelines and protocol specifications during the clinical trial.
- Organize, coordinate, and facilitate investigator meetings.
- Maintain communication with study centers, resolving issues and disseminating pertinent study trial information as required.
- Provide training for investigators, monitors, and site personnel to ensure proper handling and reporting of non-serious and serious adverse events.
- Assist in managing data flow and resolving queries as part of the study process.
Laboratory Technician
St.John's National Academy Of Health Sciences
Bengaluru
04.2022 - 12.2023
- In this role, I was tasked with the meticulous upkeep and management of laboratory equipment and clinical samples.
- I actively engage in the recruitment of eligible patients for participation in clinical trials.
- I possess the capability to effectively manage and analyze substantial volumes of data pertinent to our clinical research endeavors.
- Through my professional endeavors, I have developed a profound understanding of clinical manifestations associated with autoimmune diseases.
- My proficiency has been notably showcased through contributions to projects like ICMR funded and Investigator Initiated Projects.
- I consistently adhere to established Standard Operating Procedures (SOPs) in the execution of clinical trial projects.
- I boast a comprehensive understanding of regulatory guidelines, including the ICH-GCP E6 R2 2016 standards, as prescribed by the FDA, as well as compliance with GCLP principles, IRB submission requirements, and overarching clinical trial protocols.
- I play an integral role in coordinating site preparation for trials, conducting staff training sessions, and maintaining meticulous documentation of SOPs and Master files.
- I ensure meticulous readiness for site audits conducted by Clinical Research Associates (CRAs), Clinical Research Organizations (CROs), and other regulatory authorities.
- Despite my designation as a "lab coordinator," I have willingly embraced the responsibilities of a Clinical Research Coordinator (CRC) owing to my fervent dedication and commitment to excellence.
Project Associate
CSIR- Central Electrochemical Research Institute
Karaikudi
09.2020 - 09.2021
- Synthesis and Functionalization of Biodegradable Polymers:
Proficiently synthesize and functionalize biodegradable polymers. Utilize characterization techniques such as FTIR, NMR, DSC/TGA to analyze the chemical structure and properties of synthesized polymers. - Antimicrobial Susceptibility Testing and Data Management:
Conduct antimicrobial susceptibility testing of biomaterials, with nearly 40 samples tested on a regular basis. Collect, analyze, and manage data to understand and optimize the physical and chemical properties of the samples. - Execution of Experiments and Characterization Studies:
Lead and execute multiple experiments and characterization studies to assess the properties and performance of synthesized biomaterials. Demonstrate exceptional scientific skills and analytical abilities in executing these experiments. - Data Presentation and Milestone Achievement:
Present data in a collaborative environment, effectively communicating findings and insights. Contribute to the achievement of project milestones through timely and accurate data presentation and interpretation. - Literature Survey and Attention to Detail:
Conduct extensive literature surveys to inform experimental design and data analysis. Pay meticulous attention to detail in all aspects of the project, ensuring accuracy and reliability of results.
Quality Associate
Vision Buying Services
Tirupur
08.2018 - 08.2020
- Proficient in Managing Items and Goods:
Demonstrated expertise in managing items and goods to ensure adherence to stringent quality standards. Adept at facilitating prompt exports by streamlining processes and ensuring timely delivery. - Conducting In-Depth Inspections:
Conduct thorough inspections with meticulous attention to detail to maintain product integrity. Ensure compliance with all relevant criteria through comprehensive assessment and evaluation. - Organizing Manufacturing Processes:
Effectively organize manufacturing processes to enhance efficiency and productivity. Ensure adherence to quality standards throughout the manufacturing cycle. - Creating Thorough Reports:
Skilled in generating detailed reports to identify flaws and areas for improvement. Implement improvement plans to address identified issues and achieve quality objectives. - Achieving Quality Objectives:
Enhance compliance through strict adherence to procedures and protocols. Ensure quality objectives are met by consistently monitoring and evaluating processes. - Sample Evaluation:
Exceptional ability to evaluate samples for quality assurance purposes. Ensure product consistency and integrity through rigorous sample evaluation. - Thorough Documentation:
Maintain comprehensive documentation to track processes and ensure accountability. Facilitate transparency and traceability through meticulous record-keeping. - Promoting Continuous Improvement:
Proactively identify opportunities for improvement and implement initiatives to drive continuous enhancement. Foster a culture of continuous improvement to optimize processes and outcomes. - Assessing Suppliers:
Evaluate suppliers to ensure optimal performance and reliability. Collaborate with suppliers to achieve mutually beneficial outcomes and maintain high-quality standards. - Seeking Collaboration Opportunities:
Excited to engage with others, leveraging their insights and experiences. Explore potential areas for collaboration to enhance mutual success and achieve shared goals.
Education
Master of Science - Biotechnology
05.2018
GPA : 8.1/10
Bachelor of Science - Biotechnology
04.2016
GPA: 6.7/10
Skills
- Team building and Management
- Clinical Trial & Research
- Administration
- Data Management & Analysis
- MS Office
- SOPs, ICH-GCP E6 R2 compliance
- File Management
- Budgeting and finance
Other Activities
- At Lions Club International-Tirupur, I organized events for 'World Diabetes Day' and volunteered at 'Blood Donation' and 'Eye Clinic' camps, demonstrating my dedication to social activities and community service.
- Abstract Submissions:
1. EULAR 2024 - Evaluation and Prescription trends in Systemic Sclerosis: report of a survey among Indian Rheumatologists
2. EULAR 2024 - Predictors of persistent disease in Systemic Sclerosis: A single centre prospective observational study spanning a decade.
3. ISTH 2024 - The Spectrum of clinical and laboratory findings in Antiphospholipid syndrome at a tertiary care centre.
Certification
- ICH GCP E6 (R2) - Global Health Training Network
- GCP Certificate (NIDA CTN Network)
- Data Science and Predictive models in Public Health Research - CHES (NCHEC)
- Laboratory Risk Management (Centre for Disease Control and Prevention)
- Qualitative Research -CPH (NBPHE)
- Database management systems and bioinformatics -GRD college of science
- Training in Flowcytometry from C-CAMP, NCBS campus
- Training in Fluorescence Insitu Hybridization from Human Genetics department of St.John's Medical College.
- Training in Nail Fold Capillaroscopy from Immunology Department of St.John's Hospital.
- IELTS Academic - C1 level
- Internship on Molecular Microbiology Techniques from Centre for Biological and Nanoscience Research.
- Dissertation in Nanobiotechnology from Shankara Nethralaya research Division (VIBS)
Hobbies
- Cycling
- Hiking
- Cooking
- Photography
Languages
English
Advanced (C1)
Hindi
Intermediate (B1)
Tamil
Bilingual or Proficient (C2)
Timeline
Senior Research Associate - St.Johns National Academy Of Health Sciences
01.2024 - Current
Laboratory Technician - St.John's National Academy Of Health Sciences
04.2022 - 12.2023
Project Associate - CSIR- Central Electrochemical Research Institute
09.2020 - 09.2021
Quality Associate - Vision Buying Services
08.2018 - 08.2020
Dr.G.R.Damodaran College of Science - Master of Science, Biotechnology
Dr.G.R.Damodaran College of Science - Bachelor of Science, Biotechnology