Designing clinical trial protocols in compliance with regulatory guidelines and ethical standards.

Managing and monitoring clinical trials, ensuring adherence to protocols and timelines.

Collecting and analyzing clinical data, ensuring data integrity and accuracy.

Preparing clinical study reports and regulatory submissions for health authorities.

Collaborating with investigators, sponsors, and other stakeholders in clinical research.

Ensuring patient safety and ethical conduct in clinical trials.

Developing and implementing quality control procedures for clinical research activities.

Conducting literature reviews and staying updated on current research trends.

Managing budgets and resources for clinical research projects.

Training and mentoring junior clinical research staff.

Participating in audits and inspections by regulatory agencies.

Contributing to the development of new clinical research methodologies.

Crafting detailed clinical trial protocols, including study design, objectives, and methodology.

Collecting and analyzing clinical trial data to assess safety and efficacy of interventions.

Preparing and submitting documents to regulatory agencies like CDSCO for approvals.

Identifying and recruiting eligible patients for participation in clinical trials.

Overseeing clinical trial sites to ensure compliance with protocols and regulations.

Obtaining informed consent from patients, ensuring they understand the trial's risks and benefits.

Monitoring and reporting adverse events to ensure patient safety during clinical trials.

Conducting audits to ensure data integrity and compliance with GCP guidelines.

Staying updated with current research and publications in relevant therapeutic areas.

Collaborating with physicians, statisticians, and other healthcare professionals.

Preparing comprehensive clinical study reports for regulatory submissions and publications.

Ensuring accurate and secure data management throughout the clinical trial process.