Dr. Maahesh Kambley

I am contacting you regarding clinical research, pharmacovigilance/drug/product/ patient safety related positions. 

To brief, my educational background is Dentistry (BDS) and post graduate diploma in clinical research and management. In total, I have more than a decade of experience in healthcare/life sciences domain significantly being pharmacovigilance and clinical research. 

Currently I am working as an Assistant manager, Product owner, medical SME (Subject Matter expert), Pharmacovigilance domain consultant, internal auditor and lead trainer with TCS (Tata Consultancy services ltd, Pune, India) which is one of the leading major Pharma hubs/vendors, and KPO. Previously, I worked as a business process lead, Quality lead, trainer, SME, KOL (Key opinion leader) and Senior Drug Safety Associate (Pharmacovigilance) at TCS, Pune, India. 

The details have been mentioned in the attached resume. 

I have got an opportunity to make a significant contribution to a large, dynamic project. As a lead, individual contributor and an active member of the team, I learned to coordinate my individual efforts with the other highly motivated and talented members of the team. This experience further developed my strong organizational and team based skill sets. I am motivated to work for this opportunity as this would increase my learning bars to higher level and help me upgrade myself for benefit.

I am highly motivated and confident that my abilities would serve any organization looking for an experienced clinical research, pharmacovigilance/Drug/product safety associate/Patient Safety Specialist. 

Sincerely, 

Dr. Maahesh Kambley 

Dear Sir/Madam,  

I am contacting you regarding clinical research, pharmacovigilance/drug/product/ patient safety related positions. 

To brief, my educational background is Dentistry (BDS) and post graduate diploma in clinical research and management. In total, I have more than a decade of experience in healthcare/life sciences domain significantly being pharmacovigilance and clinical research. 

Currently I am working as an Assistant manager, Product owner, medical SME (Subject Matter expert), Pharmacovigilance domain consultant, internal auditor and lead trainer with TCS (Tata Consultancy services ltd, Pune, India) which is one of the leading major Pharma hubs/vendors, and KPO. Previously, I worked as a business process lead, Quality lead, trainer, SME, KOL (Key opinion leader) and Senior Drug Safety Associate (Pharmacovigilance) at TCS, Pune, India. 

The details have been mentioned in the attached resume. 

I have got an opportunity to make a significant contribution to a large, dynamic project. As a lead, individual contributor and an active member of the team, I learned to coordinate my individual efforts with the other highly motivated and talented members of the team. This experience further developed my strong organizational and team based skill sets. I am motivated to work for this opportunity as this would increase my learning bars to higher level and help me upgrade myself for benefit.

I am highly motivated and confident that my abilities would serve any organization looking for an experienced clinical research, pharmacovigilance/Drug/product safety associate/Patient Safety Specialist. 

Sincerely, 

Dr. Maahesh Kambley 

PSPO - I (Professional Scrum Product Owner), PMP (Project Management Professional), APGDCRM (Advanced post graduation diploma in clinical research and management)