Syed Razan Email & Phone Number

Berlin, De

Mumbai, Maharashtra, India

End to End Recruitment.

Mumbai, Maharashtra, India

I gained valuable hands-on experience in the Analytical Development Laboratory (ADL) CRD department. I honed my skills in utilizing advanced analytical techniques such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography-Mass Spectrometry (GC-MS), Gas Chromatography-Liquid Chromatography (GCLC), and wet chemistry methods.I demonstrated proficiency in operating HPLC software platforms like Empower and LabX, enabling me to conduct efficient chromatographic analyses and data processing. Additionally, I actively contributed to various projects, showcasing my ability to handle diverse tasks and work collaboratively in a dynamic laboratory environment.Through this internship, I acquired practical knowledge of Good Manufacturing Practices (GMP), Good Laboratory Practices (GLP), and other regulatory standards essential for the pharmaceutical industry. I gained insights into instrument calibration, maintenance, and troubleshooting procedures, ensuring accurate and reliable analytical results.Furthermore, I developed expertise in Standard Operating Procedure (SOP) development and validation, emphasizing my commitment to adhering to industry best practices and quality control measures. This internship experience solidified my passion for analytical chemistry and equipped me with the necessary skills to excel in future endeavors within the pharmaceutical or related industries.

Banglore

Here is a shorter summary highlighting your clinical research internship experience and fit for roles at Contract Research Organizations (CROs):During my internship at Clinilaunch Research Institute, I gained invaluable experience in Good Clinical Practices (GCP), Good Documentation Practices (GDP), pharmacovigilance, and medical scribing – essential components of clinical research and drug development.Through comprehensive training, I developed a deep understanding of GCP principles that safeguard the rights, safety, and well-being of human participants while ensuring study data integrity. I honed skills in creating and maintaining critical study documentation per stringent GDP standards, ensuring traceability and compliance.My hands-on experience in pharmacovigilance allowed me to monitor and report adverse drug reactions promptly, upholding patient safety and continuously evaluating drug risk-benefit profiles. Additionally, my medical scribing training sharpened my ability to accurately capture and document patient encounters and clinical data.This well-rounded internship prepared me to contribute significantly to clinical research projects at Contract Research Organizations (CROs). My GCP expertise ensures ethical study conduct and data quality. My GDP proficiency enables robust documentation systems and quality control measures. My pharmacovigilance skills support adverse event monitoring and regulatory compliance. Moreover, my medical scribing abilities facilitate precise data capture and reporting.Beyond technical skills, I developed strong teamwork, communication, and problem-solving abilities through collaborative projects – vital for success in CROs' dynamic environments. My attention to detail, commitment to accuracy, and passion for clinical research make me an ideal candidate to advance safe and effective therapies at CROs.

Mumbai, Maharashtra, India

Master'S Degree, Analytical Chemistry

Course, Computer Programming

Genetics, Genetics

The central dogma and Genetic Variation Mendelian Inheritance of Disease Identifying Mendelian Disease Genes Chromosomal Aberrations.

Pharmacology, Pharmacology

Drug Nomenclature Drug classes Drug modalities Pharmacokinetics | &|| Targets of drug Action Pharmacodynamics Drug Toxicity Drug Discovery.

Bachelor'S Degree, Chemistry, A

Activities and Societies: Senior Leader at National service Scheme (NSS) Member of Fine Arts and Cultural Club Blood Donation Campaign.

Course, Clinical/Medical Laboratory Science/Research And Allied Professions, 80