Avishek Bhattacharjee avishek.b@cadilapharma.com & | Responsibility involve:  Co ordinatng with PI in study and assisting in informed consent process, Patient selection ,Enroll and recruitment process based on protocol eligibility criteria basic.  Co ordinating with Sponsor during intiation ,site selection process, monitoring vist,close out process  Maintaining Study related log and forms like screening,enrollment,accountability,temperature,other communication log as per study protocol  Following up with study team for timely completion of source documents and ensuring that all relevant information required in ECRF are present in source document  Maintaining subject related source document like source visit note,Medical history,Screening,laboratory investigation as required in protocol  Co-ordinating for all lab related activities between lab and courier for shipment  Maintaning and updating the site master file and sending progress report to CRO  Maintaining the IEC related study document submission and notify all deviation and AE and SAE.  Organizing ethics and scientific committee meetings

Avishek Bhattacharjee

Responsibility involve:  Co ordinatng with PI in study and assisting in informed consent process, Patient selection ,Enroll and...

Ahmedabad, Ahmedabad, India

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Avishek Bhattacharjee’s Emails [email protected]

Avishek Bhattacharjee’s Phone Numbers No phone number available.

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Avishek Bhattacharjee’s Location Ahmedabad, Ahmedabad, India

Avishek Bhattacharjee’s Expertise Responsibility involve:  Co ordinatng with PI in study and assisting in informed consent process, Patient selection ,Enroll and recruitment process based on protocol eligibility criteria basic.  Co ordinating with Sponsor during intiation ,site selection process, monitoring vist,close out process  Maintaining Study related log and forms like screening,enrollment,accountability,temperature,other communication log as per study protocol  Following up with study team for timely completion of source documents and ensuring that all relevant information required in ECRF are present in source document  Maintaining subject related source document like source visit note,Medical history,Screening,laboratory investigation as required in protocol  Co-ordinating for all lab related activities between lab and courier for shipment  Maintaning and updating the site master file and sending progress report to CRO  Maintaining the IEC related study document submission and notify all deviation and AE and SAE.  Organizing ethics and scientific committee meetings

Avishek Bhattacharjee’s Current Industry Cadila Pharmaceuticals

Avishek Bhattacharjee’s Prior Industry
Syncorp Clinical Research | Ms Ramaiah Memorial Hospital | Lambda Therapeutic Research | Cadila Pharmaceuticals

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Work Experience

Cadila Pharmaceuticals

Clinical Research Associate

Thu Sep 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Present

Lambda Therapeutic Research

Clinical Research Associate

Fri Apr 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time) — Thu Sep 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time)

Lambda Therapeutic Research

Clinical Trial Assistant

Mon Feb 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Tue Mar 01 2022 00:00:00 GMT+0000 (Coordinated Universal Time)

Ms Ramaiah Memorial Hospital

Clinical Research Coordinator

Mon Jul 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time) — Fri Jan 01 2021 00:00:00 GMT+0000 (Coordinated Universal Time)

Syncorp Clinical Research

clinical research co orditanor

Tue May 01 2018 00:00:00 GMT+0000 (Coordinated Universal Time) — Wed May 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time)

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FAQ About Avishek Bhattacharjee

Avishek Bhattacharjee is located at
Ahmedabad, Ahmedabad, India

Avishek Bhattacharjee is a
Responsibility involve:  Co ordinatng with PI in study and assisting in informed consent process, Patient selection ,Enroll and recruitment process based on protocol eligibility criteria basic.  Co ordinating with Sponsor during intiation ,site selection process, monitoring vist,close out process  Maintaining Study related log and forms like screening,enrollment,accountability,temperature,other communication log as per study protocol  Following up with study team for timely completion of source documents and ensuring that all relevant information required in ECRF are present in source document  Maintaining subject related source document like source visit note,Medical history,Screening,laboratory investigation as required in protocol  Co-ordinating for all lab related activities between lab and courier for shipment  Maintaning and updating the site master file and sending progress report to CRO  Maintaining the IEC related study document submission and notify all deviation and AE and SAE.  Organizing ethics and scientific committee meetings Cadila Pharmaceuticals

Avishek Bhattacharjee currently works in the
Cadila Pharmaceuticals

Avishek Bhattacharjee specializes in
Responsibility involve:  Co ordinatng with PI in study and assisting in informed consent process, Patient selection ,Enroll and recruitment process based on protocol eligibility criteria basic.  Co ordinating with Sponsor during intiation ,site selection process, monitoring vist,close out process  Maintaining Study related log and forms like screening,enrollment,accountability,temperature,other communication log as per study protocol  Following up with study team for timely completion of source documents and ensuring that all relevant information required in ECRF are present in source document  Maintaining subject related source document like source visit note,Medical history,Screening,laboratory investigation as required in protocol  Co-ordinating for all lab related activities between lab and courier for shipment  Maintaning and updating the site master file and sending progress report to CRO  Maintaining the IEC related study document submission and notify all deviation and AE and SAE.  Organizing ethics and scientific committee meetings

Avishek Bhattacharjee speaks the following languages:
No languages available.

Avishek Bhattacharjee has prior experience in the following industries:
Lambda Therapeutic Research , Lambda Therapeutic Research , Ms Ramaiah Memorial Hospital , Syncorp Clinical Research

Avishek Bhattacharjee has the following professional experience:
Cadila Pharmaceuticals , Lambda Therapeutic Research , Lambda Therapeutic Research , Ms Ramaiah Memorial Hospital , Syncorp Clinical Research .