I am a clinical research professional with about 10 years of experience in the clinical research industry. I have worked in the following therapeutic areas : Oncology, Immunology, Metabolics & Virology. I have been into various site facing roles and currently, I am responsible for outsourcing processes and providing flexible solutions to the clinical operation teams in turn driving improved R & D performance and supporting the organization goals.
Training, Mentoring and coaching
Content manager for SharePoint site/s
Drug Supply Specialist
Good organization, planning, analytical and problem solving abilities
Good negotiation skills
Established interpersonal and communication skills
Strong presentation skills
11/2014 to Current
Outsourcing ManagerBristol Myers Squibb
Responsible contract management for
inhouse GDO/ MDO studies
Driving alignment to the outsourcing
strategies by interfacing with clinical operational teams, support groups &
strategic CSPs (Contract Service Providers): CROs, Central Labs, Core Labs.
03/2013 to 11/2014
Site ManagerBristol-Myers Squibb
Overall coordination and management of clinical trials from startup to closeout.
Collaboration with major functional areas to identify and evaluate fundamental issues on the project, interpret data, make good business decisions and ensure the implementation of timely solutions.
Accountability for ensuring all project deliverables
12/2011 to 03/2013
Sr. Clinical Site Monitor + Project Manager (Dual Role)Bristol-Myers Squibb
Project Manager : Responsible for the
overall management of all Clinical Investigative sites in the country for
various clinical trials conducted by BMS (India).
Developing monitoring toolsMentoring new Site Monitor/sLeading a Global Initiative on
Knowledge sharing and a global team of 22 members from various countries & Content Manager of its global
06/2009 to 11/2011
Site MonitorBristol Myers Squibb
Worked across various therapeutic areas: Oncology, Immunology, Infectious disease, and
Mentored new CRAs and was involved in development of
their monitoring activities.
Acted as the Communication Specialist
for the Hub
Drug Supply Specialist
03/2007 to 02/2010
Clinical Trial Associate and Drug Supply Specialist (Dual Role)Bristol-Myers Squibb
Administrative and Logistical support to clinical teams
Responsible for Regulatory and Ethics submissions
Resolving significant drug logistic related issues
Single point of contact for Drug supply related issues
08/2006 to 03/2007
Clinical Research CoordinatorSRL Ranbaxy Central Laboratories
Ensuring receipt of patient samples from sites across India for multiple studies, getting them processed in different departments and releasing the lab reports after thorough review
Designed and prepared Clinical Trial Presentations, Investigator's Manual
Customized lab test codes as well as the test requisition forms
Communicated & co-ordinated with the Investigator/ site team & the sponsor to ensure smooth and accurate progress of a Clinical Study from initial planning to post study closure
Education and Training
MicrobiologyThe Institute of Science, Mumbai University － MumbaiIndiaMicrobiology
Bachelor of Science: Microbiology and BiochemistrySt. Xavier's College, Mumbai University － MumbaiIndiaMicrobiology and Biochemistry
Resumes, and other information uploaded or provided by the user, are considered User Content governed by our Terms & Conditions. As such, it is not owned by us, and it is the user who retains ownership over such content.
Companies Worked For:
Bristol Myers Squibb
SRL Ranbaxy Central Laboratories
The Institute of Science, Mumbai University
St. Xavier's College, Mumbai University
Job Titles Held:
Sr. Clinical Site Monitor + Project Manager (Dual Role)
Clinical Trial Associate and Drug Supply Specialist (Dual Role)
Clinical Research Coordinator
Microbiology Bachelor of Science : Microbiology and Biochemistry
Create a job alert for [job role title] at [location].