Ria Sinha

 I am currently working as Clinical Data Analyst in Parexel International, I did master’s degree in clinical research at Indian Institute of Public Health, Delhi (IIPH-D), I also hold a Bachelor’s degree in Biotechnology. I wish to re-locating in Germany and aspire to learn and explore more in clinical data management and statistical analysis. Always open to learn new things and enhance knowledge for a better practical understanding.
I have hands on experience in platforms like Medidata Rave, Veeva Vault, Datalabs and Trial Grid. I m very much familiar with Rave environment have basic understanding of R language. Throughout my work experience, I developed skillset required for clinical data management which trained me to analyze, interpret and report data. These skills include performing UAT, query management on daily basis, completing SAS/ Offline listings monthly, preparing reports and metrics asked by sponsor, cleaning subjects, updating site status to DML along with additional responsibilities handed over to me specially at the time of DBL. I have also performed statical analysis using Stata and R and have knowledge of univariable and multivariable analysis. I have gained ICH-GCP certificated through an online course from NPTEL in NDCT, 2019. Also, I have gained knowledge of various guidelines required for conducting a clinical trial and dealing with data in a trial like ICH GCP R2, ICH GCP E2A AND E2B, NDCT 2019, GCDMP, 21CRF PART11. I have experience in all the phases of study, Start-up, Conduct and DBL.
During my coursework, I have attended workshop sample size estimation and sampling techniques and Statistical Analysis using Stata conducted by Indian Institute of Public Health, Delhi and workshop on research ethics hosted by Public Health Foundation of India (PHFI), Centre for chronic Disease Control (CCDC)& Harvard T.H. Chan School of Public Health (HSPH). I developed dissertation thesis during Master’s degree titled “Validation of genetic variants of COPD in Indian Population”.

I had my education conducted throughout in English language hence I have good fluency in English language both written and oral. I would like to apply to this job opportunity as I wish to re-locate to Germany and have no constrains, if given a chance, I would make best possible outcome from this opportunity. My passion and dedication for work bring out the sincerity required in this field, being organized, building up a research strategy and adhering to timelines support me to be a good team player and maintain a healthy working environment. I believe being open and patient for group discussion and accept different ideologies brings out the best of the group effort. My communication and leadership qualities will prove to be an asset to your esteemed institution.

I did master’s degree in clinical research at Indian Institute of Public Health, Delhi (IIPH-D), I also hold a Bachelor’s degree in Biotechnology. I wish to re-locating in Germany and aspire to learn and explore more in clinical data management and statistical analysis. Always open to learn new things and enhance knowledge for a better practical understanding.
I have hands on experience in platforms like Medidata Rave, Veeva Vault, Datalabs and Trial Grid. I m very much familiar with Rave environment have basic understanding of R language. Throughout my work experience, I developed skillset required for clinical data management which trained me to analyze, interpret and report data. These skills include performing UAT, query management on daily basis, completing SAS/ Offline listings monthly, preparing reports and metrics asked by sponsor, cleaning subjects, updating site status to DML along with additional responsibilities handed over to me specially at the time of DBL. I have also performed statical analysis using Stata and R and have knowledge of univariable and multivariable analysis. I have gained ICH-GCP certificated through an online course from NPTEL in NDCT, 2019. Also, I have gained knowledge of various guidelines required for conducting a clinical trial and dealing with data in a trial like ICH GCP R2, ICH GCP E2A AND E2B, NDCT 2019, GCDMP, 21CRF PART11. I have experience in all the phases of study, Start-up, Conduct and DBL.
During my coursework, I have attended workshop sample size estimation and sampling techniques and Statistical Analysis using Stata conducted by Indian Institute of Public Health, Delhi and workshop on research ethics hosted by Public Health Foundation of India (PHFI), Centre for chronic Disease Control (CCDC)& Harvard T.H. Chan School of Public Health (HSPH). I developed dissertation thesis during Master’s degree titled “Validation of genetic variants of COPD in Indian Population”.
I had my education conducted throughout in English language hence I have good fluency in English language both written and oral. I would like to apply to this job opportunity as I wish to re-locate to Germany and have no constrains, if given a chance, I would make best possible outcome from this opportunity.