Resume Dr.mahesh

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Dr. Mahesh Prakash Shinde Address

: Dr.Mahesh Prakash Shinde RMO, LRP Hospital and Research center, Islampur, Dist:- Sangli

Cell E-mail

: +91-9890728522/9822766473 : [email protected]

Career Objective: Utilization of technical and Clinical research skills with a progressive, dynamic organization that needs and appreciates a result oriented professional. Executive Summary:( Total 2 yrs experience) Presently working with LRP Hospital, Islampur as Residential Medical Officer. Worked as a Study coordinator in Clinical Research at Jaslok Hospital, Mumbai for HIV trials.

Software Knowledge:

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Packages Software

: MS-Office 2003/2007 [MS-Word, Excel, Power Point, Outlook] : eCRF, OCRDC and IMPALA.

Professional Qualification:

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Bachelor of Ayurveda and Medicine Surgery(B.A.M.S) Aug, 2006 from Rajiv Gandhi Univerisity Bangalore - Registration No-34428(Karnataka)

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Completed Certificate course in Clinical Research and Clinical Data Management with 2nd Rank in 2008 from Brimingham UK University.

Key Skills: 

ICH-GCP Guidelines,

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Site management

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Data management

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Trial monitoring

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Knowledge of Ethics committee

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Knowledge about protocol, CRF, ICF, IRB

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Phase III & IV Trials

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2 

QC

Achievements and Administrative Work: 

Administrating the total work of Clinical trials.

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Attended Site Initiation Visit.

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Certified in training program in OCRDC and IMPALA

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Handled trauma, surgery and Medicine department.

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Assisting for Craniotomy and Laproscopic operations.

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Assisting for Bone marrow transplantation.

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Monitoring and ventilatory care of emergency patients.

Clinical Research Experience: Worked as a study coordinator for two clinical research trials on HIV at Jaslok Hospital and Research Center Mumbai, with Dr.J.K.Maniar

Responsibilities of Trial 1:A multi-centre, open label, expanded phase 3b trial on HIV

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Pre-screening of subjects.

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Consenting the subject.

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Screening assessment.

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Recruitment of only those subject who fulfil protocol required criteria.

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Follow up of subjects on their scheduled visit.

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Dispensing of medication.

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Assessment of all parameters at all visit.

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Maintaining the lab reports.

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Instructing the caregiver or parents regarding use of medication.

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Physical examination of subject enrolled in study.

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Documentation in source notes & case report form or Electronic database.

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Reporting serious adverse events to sponsor & Ethics committee. within specified time lines

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Regular correspondence with sponsor & Ethics committee.

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Maintaining temperature records for investigational product. Accountability of study products, Blood collection at scheduled visits.

Responsibilities of Trial 2:A Multi-centre survey of HIV 1 viral co-receptor tropism in patients infected with clade C HIV-1 at select sites in India •

Informed consent,

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eCRF completion and correction,

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Sign –off data queries,

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Vital signs,

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Specimen collection.

Work Experience at Hospital: •

One year Internship from Shri. S.B.S Ayurvedic Medical College’s Hospital Mundargi, Dist – Gadag, Karnataka, India.

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Worked as a Medical Officer at Prachi Pediatric Hospital, Kolhapur, Maharashtra, India.

AREAS OF INTEREST:     

Clinical Trials Data Management Epidemiological Disease HIV-AIDS Preventive and Social Medicine

STRENGTHS:    

Good communication skill. Hard work Ability to work in team. Handle the crises.

Personal Details Date of Birth

: 27th June, 1983

Sex

: Male

Marital Status

: Unmarried

Other Interests Languages Known

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: Playing Chess, Reading. : English, Hindi, Marathi, Kannada.

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References Dr.Reena Verma (Co-Investigator) Jaslok Hospital & Research Center, Mumbai

+91 9821314418

Mr. Tapankumar Shah (CTL) Pfizer Limited,Mumbai

+91 9967055228

Mrs. N. Shrividhya (CRA) Parexel International (India) Pvt.Ltd, Bangalore

+91 9901133455

Dr.Promad Patil (Medical Director) LRP Hospital & Research Center, Islampur

+91 9271216944

Dr. Mahesh P. Shinde

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