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  Provides major contributions to business development and proposal preparation Demonstrates expertise within the project. Shares clinical data knowledge across the project teamand to the client, incorporating project and industry expertise Demonstrates advanced knowledge (financial and project related) of all internal processes requiredto manage various RWD projects and guides team accordingly Identify new business opportunities and is motivated to engage with clients. Supports the accountmanagement process and plans. Supports new business opportunities

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 to handle various EHR data-sets Managed programs and new initiatives as an SME Supported team in the presales activties (concept note and proposal development)Represented project at sponsor, investigator, training or safety review meetings,Managed project resources (i.e., budget, personnel, and subcontracts) to ensure that project tasks areperformed efficiently and on a timely basisInvolved in setting-up of clinical (Late phase) studies across Europe

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 project management and execution of the project Lead study start-up activities and assist in review and finalization of study and project-related documents Involve in development for concept note and project proposals for new business  Manage contracted CROs in the overall activities of the project Review project budgets, team assignments and project deliverables with the overall project timelines  Involve in the setup and conducting training to project teams, vendors and stakeholders on need basis Supervision of monitoring and remote data evaluation activities which may involve site visits Contribute on review and writing aspects of in-house journals

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 teams and vendors- Review project budgets, team assignments and project deliverables.- Set up, execution, monitor, quality check and final delivery of completed study to the clients.- Project Management support to sponsor– whole, as a functional service provider e.g. Operational execution, Patient Recruitment & Retention Services and etc

 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 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)

• 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