Uttam Barick Email & Phone Number

Singapore, Bangalore

India/Singapore

Bangalore

Trains, develops and evaluates study personnel to ensure efficient project operation Designs and implements efficient work processes, schedules and checklists to ensure routine clinicaltrial and other project activities are performed in accordance with corporate, project-specificStandard Operating Procedures (SOPs) and applicable regulatory agencies .

Bangalore Area, India

Served as primary point of contact for the Sponsor and External Investigators for operational activities of a Hybrid clinical trialCoordinated activities of cross-functional teams and oversees operational, data management,regulatory, monitoring, and protocol development processes associated with the projectsContributed to setting up an RWD infrastructure.

Bangalore

Bangalore

 Managing and consulting in the overall setup of Real World Evidence and late phase studies (MARKET ACCESS) end to end activities across Europe, Middle East and APAC region  Serving as a subject matter expert on reviewing and executing contracts/grants of clinical experts and key stakeholders of the study Work closely with the Sponsor for central.

Bangalore

Managing and consulting clinical studies (Respiratory & Infectious diseases) in Europe & APAC.

Bangkok, Thailand

- Montoring and developing cross country International sites- Manage team of associates across India,Thailand and Bangladesh, - Work closely with Sponsor for project management activity.- One point of contact for Sponsor company for the central project management.- Manage electronic data for global studies across all regions.- Deliver trainings to project.

 Monitor the conduct of clinical trials, especially enrollment and quality of data. Verify subject safety and site adherence to specific regulations and ICH/GCP Guidelines. Ensure Adverse Events are reported appropriately, accurately and in a timely manner and that follow-up activities are conducted as necessary. Manage site master file contents and.

• Verify subject safety and site adherence to specific regulations and ICH/GCP Guidelines.
• Ensure Adverse Events are reported appropriately, accurately and in a timely manner and that follow-up activities are conducted as necessary.
• Manage site master file contents and work with sites to ensure communication requirements between site and IEC/IRB are adhered to.
• Assist with other administrative and special projects, as required (e.g. planning of investigators and training meetings; participating in presentation at meetings)

Msc, Clinical Research

Professional Course - completed thesis work on Ethics Commitee

Pgdpm, Pharmaceutical Management

PGDPM (Pharmaceutical Management)

B.Sc, Biotechnology

Biotechnology

Puc, Pcmb

Activities and Societies: AMPSCompleted my 10th Std