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Dr. Mahesh Prakash ShindeAddress : 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 9967055228Pfizer Limited,Mumbai

Mrs. N. Shrividhya (CRA) +91 9901133455Parexel International (India) Pvt.Ltd,

Bangalore

Dr.Promad Patil (Medical Director) +91 9271216944LRP Hospital & Research Center,Islampur

  Dr. Mahesh P. Shinde

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