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Dr. Manish Patel, M.B B.S, D.C.P C. V.: 33 Shreshth HP Petrol Pump

Dr. Manish Patel is a senior manager at Lambda Therapeutic Research Ltd. with extensive experience in clinical laboratory management and pharmacology. He has held various roles in clinical research, including co-investigator in clinical trials and safety management of subjects. Dr. Patel is also well-educated with an MBBS and D.C.P., and has participated in numerous workshops and conferences related to pathology and clinical research.

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Pankaj Nathvani
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13 views3 pages

Dr. Manish Patel, M.B B.S, D.C.P C. V.: 33 Shreshth HP Petrol Pump

Dr. Manish Patel is a senior manager at Lambda Therapeutic Research Ltd. with extensive experience in clinical laboratory management and pharmacology. He has held various roles in clinical research, including co-investigator in clinical trials and safety management of subjects. Dr. Patel is also well-educated with an MBBS and D.C.P., and has participated in numerous workshops and conferences related to pathology and clinical research.

Uploaded by

Pankaj Nathvani
Copyright
© © All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
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Download as PDF, TXT or read online on Scribd
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Dr. Manish Patel, M.B;B.S, D.C.P C. V.

Address: 33 Shreshth Bungalows


Behind HP PETROL PUMP
Motera Road,
Sabarmati,
Ahmedabad-380005.
Tel.: 09825263270. 9723290184

PROFESSIONAL EXPERIENCE
Lambda Therapeutic Research Ltd. Clinical laboratory Senior Manager March 2020-
present Authorization of all Laboratory reports of Hematology, biochemistry, immunology,
urinalysis Clinical pharmacology & medical affairs
dept. Senior Manager
Ahmedabad, India (October 2002-March2020 )
Lambda Therapeutic Research Ltd.
As contractual duty doctor from September 2000 – September 2002
Green Cross-Laboratory, Ahmedabad.
Gujarat, India.
Pathologist (January 1998 – December 1998)
Sarvajanik Hospital :100 beded with ICU, Gozaria, Mehsana Gujarat, India
Physician and Pathologist (April 1999 – August2000)
Senior Manager-CPMA
Act as a Manager volunteer recruitment & screening,Feasibility Inputs and safety review for all
the protocols ,To handle store and accountability of emergency medicines.Report generation,
checking of completeness of the adverse events,In charge of screening at Ahmedabad facility,
Clinical examination and determining eligibility of subjects in all clinical studies.
Co-investigator in Phase –I ,II/III & BA/BE clinical trials
Investigator in MD-MV trials ,Compliance to Protocol & SOPs
Support Clinical Trial group & Help for corporate check-up
Safety management of the subjects and its documentation,Management of Adverse Events,
Phlebotomy and checking of Medical screening records,Preparing protocols for
bioavailibility/bioequivalance studies and clinical trial with special inputs in the safety review of
the protocol.
Reporting to the ethics committee. & Conduct of consent process and explaining subject
related queries and its documentation.Consent for screening and its documentation To coordinate
the conduct of CPR Training Programme and other safety related training
programmes.Maintenance of Medical confidential reports and their follow-ups. Arrangement and
training of contractual Doctors
Inputs and safety review for all the protocols ,To handle store and accountability of emergency
medicines.Report generation, checking of completeness of the adverse events
Pre study:
Help to Prepare protocol and its appendices,
Communicate with medical writing team & sponsor on all projects related issues,Conduct study
consent process & Check data ,Train the study personnel on project related activities,Ensure
arrangement of contractual staff , proper initiation and conduct of the trial
During study:
Check all forms including consent forms,Communicate with sponsor and other departments on
appropriate aspects of the clinical studies ,Ensure proper documentation of Adverse Drug Reaction,
Note to files, Deviations etc. Co-ordinate QA audits & Send clinical updates to all concerned ,Ensure
subject contact during washout period and follow-ups
Post study:
Handle subject compensation & Follow up unresolved adverse events ,Check all the forms &
Compile raw data and prepare reports
Resolve all QA queries in timely manner & Prepare and verify all clinical binder

Safety Issues:
Tracking of adverse events and safety issues reporting. To keep tract of to arrange for safety follow
up for the staff (e.g. Vaccination schedule etc.) Sanitation and hygiene supervision of the clinical
facility. Supervision of handling and disposal of biological waste. IEC communication: For adverse
events, clinical updates. To help maintain and update all the systems and SOPs in the departmentAny
other responsibility as designated from time to time by the Head of the Department.
SPECIAL EXPERIENCE
Investigative procedures including Lumbar puncture, and bone marrow aspiration.Transfusion of
blood and Peritoneal Tap. Special experience in FNAC,Fluid cytology & Peritoneal dialysis.
Working for the patients below poverty line & Experience in blood banking and blood donation
camps & Knowledge of MS-office, Excel and Internet.
CONFERENCES AND WORKSHOPS
National Pathology Update Pune Nov 1999
GCP WORKSHOPS AHMEDABAD 2001 TO 2019 Once in every
year
Quality management in Ahmedabad Nov 2003
Blood Transfusion -Prathma
International Workshop on Pune Nov 2004
Clinical Research
Management and Clinical
Data Management
DCGI workshop on ‘Clinical Mumbai Nov 2006
Research -What is preached’
ACLS & BLS Ahmedabad 2008 ,2012
All India Conference of Gandhinagar Dec 2009
Pharmacology
Advanced GCP workshop Ahmedabad October 2011,2013

EDUCATIONAL QUALIFICATION
❖ MBBS from B.J. Medical College, Ahmedabad, India. Registration No. G-23675
❖ One-year internship at B.J. Medical College, Ahmedabad, India.
❖ D.C.P. from MP Shah Medical College, Jamnagar, Gujarat, India.
LANGUAGES KNOWN:
English, Hindi, Gujarati Date of Birth 19-09-1971 ,Married

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