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Dr. Mahesh Prakash Shinde


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

Cell : +91-9890728522/9822766473
E-mail : mahesh_research@rediffmail.com

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:

 Packages : MS-Office 2003/2007 [MS-Word, Excel, Power Point, Outlook]


 Software : eCRF, OCRDC and IMPALA.

Professional Qualification:

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

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

Key Skills:

 ICH-GCP Guidelines,

 Site management

 Data management

 Trial monitoring

 Knowledge of Ethics committee

 Knowledge about protocol, CRF, ICF, IRB

 Phase III & IV Trials

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 QC

Achievements and Administrative Work:


 Administrating the total work of Clinical trials.

 Attended Site Initiation Visit.

 Certified in training program in OCRDC and IMPALA

 Handled trauma, surgery and Medicine department.


 Assisting for Craniotomy and Laproscopic operations.
 Assisting for Bone marrow transplantation.

 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

 Pre-screening of subjects.

 Consenting the subject.

 Screening assessment.

 Recruitment of only those subject who fulfil protocol required criteria.

 Follow up of subjects on their scheduled visit.

 Dispensing of medication.

 Assessment of all parameters at all visit.

 Maintaining the lab reports.

 Instructing the caregiver or parents regarding use of medication.

 Physical examination of subject enrolled in study.

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

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

 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,
• eCRF completion and correction,
• Sign –off data queries,
• Vital signs,
• Specimen collection.

Work Experience at Hospital:

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

• 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 : Playing Chess, Reading.

Languages Known : English, Hindi, Marathi, Kannada.

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References

Dr.Reena Verma (Co-Investigator) +91 9821314418


Jaslok Hospital & Research Center,
Mumbai

Mr. Tapankumar Shah (CTL) +91 9967055228


Pfizer Limited,Mumbai

Mrs. N. Shrividhya (CRA) +91 9901133455


Parexel International (India) Pvt.Ltd,
Bangalore

Dr.Promad Patil (Medical Director) +91 9271216944


LRP Hospital & Research Center,
Islampur

Dr. Mahesh P. Shinde

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