Anilkumar Kothapalli

Skilled clinical research Associate with background in managing and overseeing clinical trials. Experience includes coordinating with research teams, ensuring compliance with protocols, and managing participant recruitment and data collection processes. Possess strong organizational skills, ability to manage multiple tasks efficiently, and capability to ensure accuracy in documentation and reporting. Contributed to improving trial procedures and enhancing data integrity in previous roles. Efficient and focused professional in clinical research management. Known for high productivity and ability to complete tasks efficiently, ensuring timely project advancements. Skilled in patient recruitment strategies, regulatory compliance, and data analysis. Excel at communication, teamwork, and problem-solving to drive successful outcomes in complex research environments.

• Pharmacist, State Government Pharmacy, Guntur, AP, India.
• Clinical Research Trainee, Andhra University of Sciences Research Organization, Andhra Pradesh, AP, India.
• Worked as a clinical oncology Assistant goverment hospital.

1. Observation on Efficacy and Safety of Chloroquine vs. Artesunate in the Treatment of Vivax Malaria in Pediatric Patients, Conducted a comprehensive hospital-based study to assess the comparative effectiveness and safety of Chloroquine and Artesunate in treating pediatric patients with Vivax Malaria. 

2. Childhood Obesity and its Physical and Mental Health Comorbidities, Undertook a systematic review exploring the prevalence, factors, and associated physical and mental health comorbidities of childhood obesity among Australian children.

• Clinical Research Associate
• Pharmaceuticals Medical Research
• Patient Care Clinical Trial
• Site management
• study protocol and compliance
• Study monitoring and reporting

• Understanding of clinical trial phases (I-IV).
  Knowledge of Good Clinical Practice (GCP) and (ICH) guidelines.
• Familiarity with FDA, EMA, and local regulatory authority requirements.
  Awareness of ethics committee approvals and informed consent processes.
• Understanding of Clinical Data Management Systems (CDMS) like Medidata, Oracle, or REDCap.
• Familiarity with statistical analysis tools and concepts.
• Site initiation, monitoring, and close-out visit expertise.
• Ability to verify data accuracy and compliance.
• Collaborating with site staff, sponsors, and cross-functional teams.
• Effective oral and written communication skills for clear reporting.
  

• Data driven analytical thinking and conceptual problem-solving ability.
• Trust, integrity and commitment to my work.
• Collaboration and relationship building ability.
• Insist on the highest quality of my work.
• Planning and organising ability including prioritising, task delegating and project management skills.
• Self-motivated and disciplined.