Qualification - MBBS / MD
Fresher can apply if looking for career in Clinical Research
Medical Monitoring
Medical Monitoring at site level is comprised of review of Site Investigator File, Safety and SAE reporting documents, Laboratory documents and reports, X-ray and ECG reports.
Medical monitoring performed remotely at Lambda Office comprises of providing guidance, if required by PI/study team, which will include, but not be limited to, eligibility criteria, study procedures and patient continuation and discontinuation. It also comprises of reviewing the adverse events and Reliable Adverse Events (SAEs) documents, occurring in the trial and ensure proper recording and reporting of the same.
Secondary
Feasibility grid preparation




Preparing the feasibility for the Clinical trials as per the requirement of the sponsors.
Reviewing Feasibility Questionnaires and feasibility reports.
Medical Writing
Training
Train the study team members of the study protocols and other study related documents.
Train the members of the department on the various therapeutic / technical areas
Site initiation visits.
General Duties
Keep abreast with the development in the field of clinical research in India and overseas.
Comply with quality initiatives designed by the department.

Interested for send cb this mail ( Email [email protected] )

📌 Clinical Research (Ahmedabad)
🏢 Nameless
📍 Ahmedabad