Ask Question / Post resume

Post a reply to the thread: Indegene LifeSystems Pvt Ltd Bangalore, Delhi, Mumbai : Copywriter

Your Message

Your Username:

Notes:-
1) You can copy and paste your full resume in the box below.
2) Or you can ask your question. We try to answer, as far as possible.

Title:

[QUOTE=ashwinkumar1706@yaho;39181]RESUME

ASHWINIKUMAR R. INGALE.

Career Objective: 
Seeks an appropriate position for working with an organization having a strong vision & mission to enhance its growth & development providing simultaneous opportunities for strengthening the foundation of myself & further enhance my knowledge. 
 
Educational Qualifications:- 
- Post Graduate Advance Diploma in Clinical Research (PGDACR). Institute of Clinical Research of India , Andheri

- B. Pharmacy 
(North Maharashtra University, Jalgaon) -2002 from Collage of Pharmacy, Faizpur with 57.40% in the final year.

- Diploma in Medical Laboratory Technology (D.M.L.T).-1998 From New Delhi with first class, first Rank.

- Diploma in Pharmacy 
(B.T.E. Mumbai)-1997 from Institute of Pharmacy, Faizpur with 57.80% in the final year.

Additional Qualifications / Skills: 
- MS-Office (Word, Excel, Power Point, Internet Concepts)
- FDA Approval in Tablets Manufacturing Section at Ajanta Pharma Limited, Paithan

Job Responsibility:¬ -
- Responsible for activities involved in the conduct of Clinical trial.
- Comply with company policies, SOPs & regulatory guidelines
- Ensuring that the source notes are according to the ICH-GCP requirements.
- Coordinating site initiation visits, submission of study protocols & other documents to ethics committee.
- Performing site drug accountability, checking that the study drugs are appropriately stored and dispensed, ensuring the drug dispensing records & temperature logs are up to date and monitoring expiry dates of study supplies 
- To coordinate between local / central laboratory and courier for the shipment and collection of study material
- Update patient tracking log to the sponsor company
- Assuring adequate reporting of adverse events and ensuring that the collection of data from medical records, subject interviews, questionnaires, diagnostic tests and other sources are complete and reported accurately
- Follow established guidelines in the collection of study data and respond to study procedures/protocol questions
- Works closely with Project Manager, Sponsor’s CRA as appropriate, training & QC Managers, Medical associates
- Maintaining strict confidentiality about study protocol, study drug and study procedures & SOPs
- CRF (Case Report Form) completion
- Track the flow of regulatory documents for all projects responsible for in order to co-ordinate and deliver the appropriate regulatory documents to meet regulatory and Ethics Committee submission dates
- Assist Principal Investigator in patient selection and clinical research study
- Patient’s follow-ups
- Ensuring protocol complaints at the centre
- All other administrative support to the Principal Investigator

Work Experience: 
- Worked as Production Executive (Coordinator) in Shalina laboratories Pvt. Ltd. Mar 2008 to sep 2008. 
- Worked as Production officer in M.J. Biopharm. Pvt. Ltd Navi Mumbai from Sep 2007- Mar 2008. 
- Worked as Jr. Production officer in Ajanta Pharma Ltd. Paithan Dist-Aurangabad. From Oct 2005 to Aug 2007 
- Worked as Production officer in Khandelwal Laboratories Ltd Vapi (Gujarat), From Aug 2004 to Sep 2005. 
- Worked as Trainee Production supervisor in Niramay Pharma Pvt. Ltd, Nashik, From Dec 2002 to Aug 2004. 
 Personal Details:-

Hobbies/Interests: Listening music, surfing internet, Traveling.

Date of birth: 17th June 1977
Nationality: Indian.
Gender: Male
Marital Status: Married
Languages: English, Hindi, Marathi[/QUOTE]

All times are GMT +5.5. The time now is 01:27 AM.